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ISEB-SWTINT1 - ISEB Intermediate Certificate in(R) Software Testing - BrainDump Information

Vendor Name : ISEB
Exam Code : ISEB-SWTINT1
Exam Name : ISEB Intermediate Certificate in(R) Software Testing
Questions and Answers : 43 Q & A
Updated On : January 17, 2019
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ISEB-SWTINT1 exam Dumps Source : ISEB Intermediate Certificate in(R) Software Testing

Test Code : ISEB-SWTINT1
Test Name : ISEB Intermediate Certificate in(R) Software Testing
Vendor Name : ISEB
Q&A : 43 Real Questions

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ISEB ISEB Intermediate Certificate in(R)

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The ISEB verify administration certification is the next level of competency in software trying out after the ISEB groundwork and ISEB Intermediate stages. earning this certification makes employment candidates more constructive and marketable, because it signifies a strong means to analyse, synthesize and evaluate tasks related to utility testing management. These talents are crucial to the profession development of software testers, exceptionally in this age of global competition and economic uncertainty.

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what is an ISEB certificates? | killexams.com Real Questions and Pass4sure dumps

what's an ISEB supervisor's certificates in IT provider administration? and can you inform me what ITIL is? These both had been requested in a recent job description.For counsel in regards to the ISEB supervisor's certificate in IT carrier management, please see this internet website. you are going to also wish to read the instructions at this web page.

as far as i can tell, here's an expert construction effort that combines working towards and checks to advance already-certified managers -- who need to first obtain an ISEB/EXIN groundwork certificates in IT service management (or the ISEB network carrier administration certificate, which offers exemption) -- into more senior certifications in the selected areas of service aid or carrier start.

so far as ITIL goes, that refers to the IT Infrastructure Library, a mostly European strategy to managing IT functions, supported via British regular 15000 (BS15000). See this web web page for greater assistance.

It sounds like you're on account that employment somewhere in the European Union, if no longer within the UK. respectable good fortune and hope that helps!


ISEB Practitioner enterprise and answer structure | killexams.com Real Questions and Pass4sure dumps

This seller-certain Certification is offered via:British desktop Society (BCS)Swindon, Se UKPhone: 44 (0)1793 417417

ability degree: superior                          fame: lively

affordable: no longer obtainable               

summary:For commercial enterprise and answer Architects who observe their intermediate degree competencies to a case analyze and might difficult on the agency and processes required to manage an architecture efficaciously. This certification is proper for those that are engaged in any factor of commercial enterprise and answer structure.

initial requirements:You have to pass the ISEB Practitioner in business and answer structure exam. The examination has a one hour time limit and carries 40 dissimilar-alternative questions in keeping with a case study. A passing score of 26/forty is required.Six years of IS/IT work experience, including some architecture definition is advised. it's additionally counseled you cling the ISEB Intermediate degree certificates, or have studied the ISEB Intermediate level Syllabus and Reference model, and have both TOGAF 8 or TOGAF 9 degree 2 certificate. working towards is purchasable however not required.

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ISEB-SWTINT1 exam Dumps Source : ISEB Intermediate Certificate in(R) Software Testing

Test Code : ISEB-SWTINT1
Test Name : ISEB Intermediate Certificate in(R) Software Testing
Vendor Name : ISEB
Q&A : 43 Real Questions

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Digitization of multistep organic synthesis in reactionware for on-demand pharmaceuticals | killexams.com real questions and Pass4sure dumps

A plastic plan for organic synthesis

The infrastructure for chemical synthesis typically lies at either end of a spectrum: small-scale studies in ad hoc assemblies of glassware or large-scale production in capital-intensive custom reactors. Kitson et al. report a hybrid protocol that customizes a blueprint for synthesis of a target compound in a series of interconnected plastic modules, which can be assembled en masse by 3D printing (see the Perspective by Hornung). The approach, demonstrated for the commercial muscle relaxant baclofen, establishes a systematic workflow that is potentially amenable to automation: All that is necessary for synthesis and purification is the introduction of stock solutions and variation of temperature or pressure.

Science, this issue p. 314; see also p. 273

Abstract

Chemical manufacturing is often done at large facilities that require a sizable capital investment and then produce key compounds for a finite period. We present an approach to the manufacturing of fine chemicals and pharmaceuticals in a self-contained plastic reactionware device. The device was designed and constructed by using a chemical to computer-automated design (ChemCAD) approach that enables the translation of traditional bench-scale synthesis into a platform-independent digital code. This in turn guides production of a three-dimensional printed device that encloses the entire synthetic route internally via simple operations. We demonstrate the approach for the γ-aminobutyric acid receptor agonist, (±)-baclofen, establishing a concept that paves the way for the local manufacture of drugs outside of specialist facilities.

The manufacture of active pharmaceutical ingredients (APIs) is vital for modern health care, yet critical drugs are regularly manufactured for a finite period in a limited number of sites. The manufacture of chemical products—whether bulk, fine, or specialty chemicals, such as APIs—is currently based on a model whereby a central plant is exclusively designed for the manufacture of the product, or range of products, sold by that particular company (1). This model holds whether the manufacturer is a large pharmaceutical company or, as is increasingly the case, a contract research organization operating large chemical manufacturing plants to order from the pharmaceutical industry. This process leads to safety issues around both the storage and transport of such materials, as well as the issues inherent in the large-scale manufacture of chemicals (2). In addition, these large-scale plants are often at the mercy of complicated and global supply chains of raw materials, the failure of which at any point will reduce or halt the capacity of the plant to produce materials and deliver them effectively (3, 4). Also, when a given complex intermediate or API goes out of production, the plants are often repurposed and the manufacturing capacity is lost. The reinstatement of the process would require, in the best case, substantial capital investment to reconfigure a chemical plant for its synthesis. To alleviate this issue, we propose a concept whereby the large-scale manufacturing process of complex fine chemicals, such as APIs, is augmented by distributed, point-of-use manufacturing in self-contained cartridges, requiring limited user interaction to produce the desired products on demand. To achieve this, we developed a methodology for the translation of bench-scale synthesis procedures into a step-by-step workflow that could be used to create digital designs for custom reactionware that can be fabricated by using three-dimensional (3D) printing technologies. In this way, we aim to move beyond the preserve of industrial manufacturing and prototyping applications (5), to revolutionize the relationship between the design, manufacture, and operation of functional devices (6–11) and exploit the increasing use of 3D printing in the automation of the chemical sciences (12–15). This methodology, which is in stark contrast to both large- and medium-scale traditional chemical manufacture, and also to the use of continuous-flow and microreactor approaches (1, 16, 17), allows for the distribution of simple chemical precursors and solvents rather than the complex products themselves. These precursors could then continue to benefit from the economies of scale brought by traditional manufacturing processes while complex products with short shelf lives, or lower and more distributed demand, can be produced locally. This has added benefits in terms of manufacture of the final products as the synthesis of smaller quantities is inherently safer than large-scale processes and poses less risk to both operators and infrastructure. Further, the translation of these synthetic approaches into a digitally defined format, where the reactor design and, eventually, an automated synthesis procedure are encoded, could allow the digitization of all chemical products into a very low-cost manufacturing format. This could allow large numbers of discontinued APIs to be made available as they can be brought back into production on a small scale by the fabrication and use of the appropriate cartridges (18, 19).

As a proof of principle, we present a process by which the traditional laboratory-scale synthesis of a commercially available API can be translated into the design of an integrated cartridge. To do this, all the reaction steps and intrasynthesis purification processes are encoded into the 3D architecture of the cartridge so that the chemical reactions, work-ups, and purification are done with minimal user intervention and exposure automatically. We have demonstrated this process in the full synthesis of the anticonvulsant medication (±)-baclofen (see below).

This method for translating traditional laboratory syntheses into a form that can be encapsulated in a single cartridge is split into three layers of consideration, which were iteratively reevaluated during the cartridge development process. The first is the “conceptual layer,” where the chemical reactions and processes necessary are identified and developed. The second is the “digital layer,” in which these processes are translated into digital 3D models of the final cartridge devices. Finally, a “physical layer,” where the digital models are realized as either a modular implementation or a monolithic implementation, is used to generate the finalized cartridge, which can be used to effect the designed synthesis (Fig. 1). These physical systems can then be tested for efficacy as a final implementation, before iterating the process to develop reliable cartridge syntheses.

Fig. 1 Schematic representation of the translation of a multistep synthesis from conception through to implementation as a reaction cartridge.

Reactions necessary for the synthesis are identified (A→B→C→D, top left panel) and the specific chemical and physical processes and reaction parameters necessary for each reaction are laid out (conditions i. – iii., left panel). These processes are then translated into bespoke reaction modules designed to accomplish one or more of the chemical processes identified in the previous step (top right panel). The modules are then designed as 3D CAD models (lower center panel), with libraries of module components to accommodate the required reaction parameters. These digital models can then be fabricated to produce either a modular or monolithic implementation (lower right panel) of the process.

First, the fundamental chemistry required for the transformations is considered and optimized to minimize the necessary interstep purification for the completion of the full synthesis. This approach is similar to that taken to develop telescoped (i.e., consecutive transformations in a single reactor or sequence of reactors without isolation and purification of intermediates) and “one-pot” syntheses (20, 21), often used in process chemistry, both of which aim to maximize the efficiency of the synthetic route. Although here it is not necessary to produce genuinely telescoped syntheses, as modules for interstep purification can be built into the cartridge design, the synthesis of the desired compound, including all reagents and starting materials for all the necessary steps, must be considered as a unified process. The choice of synthetic route to any target compound will be dictated by a number of factors, including the relative availability and cost of starting materials, reagents, and solvents, as well as the compatibility of reaction and purification sequences with the reactor modules produced. In any wide-scale application of our approach, a cost analysis of any proposed synthetic route will have to be performed to ensure its viability for the product. Once the chemistry for the synthesis is developed, a sequence can be produced where the physical processes and reaction parameters—such as heating, cooling, phase separations, reaction volumes, and times—can be identified.

Vital to the success of these modules is the compatibility of the cartridge material with the chemistry being performed. Whereas traditional laboratory syntheses take place mostly in glassware, we use polypropylene (PP) as a basic structural material for the fabrication of the cartridges. We have found that this polyolefinic material, while demonstrating a robust range of chemical compatibility for traditional synthetic organic reactions, is also a suitable substrate for 3D printing applications (22–24). This gives the best balance of chemical resistance and material properties for 3D printing. Therefore, the first step in the design process is testing the reactions necessary for compatibility in the reactor materials. Future iterations of the concept could expand on the materials and fabrication processes available for the reaction modules to further develop the range of chemistries feasible in this system, using, for example, perfluorinated polymers to increase the chemical resistance of the module.

To demonstrate the feasibility of incorporating these PP reactors into the production of APIs, we tested a number of reactions that lead to such targets in test modules fabricated from PP (Fig. 2). We tested reactions for the synthesis of three APIs: the central nervous system inhibitor (±)-baclofen (25), the anticonvulsant lamotrigine (26), and the gastroprotective agent zolimidine (27). As can be seen, all of the reactions tested were observed to work, but with slightly lower efficiency in PP reactors than in traditional glass reactors, owing to physical loss of material on the relatively rough PP surface hampering product recovery. Surface roughness is inherent in the 3D printed process; however, use of other, as yet undeveloped, materials or different manufacturing techniques could reduce this issue. The zolimidine reactions, particularly the copper-catalyzed iodination reaction, experienced a pronounced reduction in efficiency, compared to (±)-baclofen or lamotrigine. We surmised that this was due to side reactions of the iodine with the polypropylene. These issues highlight that the process of translation from glassware must take into account both the physical and chemical properties and limitations of the reactor substrate (23). For this reason, the first two syntheses were selected for further development into reaction cartridges to explore the concept.

Fig. 2 Comparison of glass reactors with plastic reactionware for the optimized synthetic routes to (±)-baclofen (top), lamotrigine (middle), and zolimidine (bottom) with reaction yields for each step (reaction yields in PP vessels given in parentheses).

Single (top right) or double (bottom right) chambered polypropylene reaction test cartridges were used. PP, polypropylene; TBAF, tetrabutylammonium fluoride; THF, tetrahydrofuran.

Once the processes needed for the reaction sequence are identified, the combined continuous protocol is mapped onto the 3D digital designs for the target-specific cartridge. The sequence of processes is split into a series of modules, with each representing a telescoped series of processes that can take place in a single chamber of the 3D printed system. Each process module is then created as a digital model that can be manipulated to provide the correct physical dimensions necessary for the reaction scheme. The 3D models of the cartridges used in this study were created with OpenSCAD software, an open-source framework for CSG (constructive solid geometry) modeling that allows a highly flexible and configurable approach to create versatile libraries of components as reusable pieces of code. Once defined, these pieces of code can be manipulated by the software, allowing the generation of complex reactor geometries with minimal human inputs. For example, in this study, we designed a module library consisting of interchangeable top and bottom components with varying features that can be easily combined to produce reaction vessels with different shapes and features. From a single line of code, an entire module can be created, with 18 different shapes available (i.e., three different tops and six different bottoms can be selected; Fig. 3). The modules were designed around simple chambers where each reaction or process could be performed in as close a manner as possible to the way it would be carried out with traditional batch chemical techniques, easing the transition between published synthesis in glassware and “cartridge” synthesis. Typically, a standard module would have an opening on the top of the wall of the chamber for transfer of reaction mixtures from previous modules and an opening at the bottom of the chamber for expelling material from the module subsequent to the completion of the desired process. The transfer of material between modules is facilitated by a further opening in the roof of the compartment, which can be used to apply pressure that forces the reaction medium out of the chamber via the outlet at the bottom. The opening at the top otherwise equalizes pressure throughout the device to prevent the premature transfer of material, and also allows for application of vacuum to remove and exchange solvents. These modules can then be combined in sequences by use of further components of our module library such as siphon tubes for the transfer of material from one reaction module to another.

Fig. 3 Parameterized approach to the design of individual process modules.

Digital libraries of module components (top) can be easily assembled to produce a wide range of module geometries dictated by the specific process and reaction parameters (e.g., solvent volumes, number of inputs and outputs, etc.) (bottom). Hydrophobic filters for phase separation are shown in red, and fritted glass filters are shown in blue. DCM, dichloromethane. HR, reactor height.

Once a reaction chamber is created, new features can be introduced by subtracting or adding shapes to the module. For example, a filtration device can be made from a module with a top input, a round bottom with a port, and a glass filter. To achieve this feature, a cylindrical model conforming to the dimensions of the physical filter to be inserted is created and subsequently subtracted from the model of a reaction chamber, producing a void space in the model into which the filter fits (see supplementary materials). Phase separation modules were achieved in a similar manner by using hydrophobic frit inserts that effectively separate organic and aqueous phases for product extractions. In keeping with our desire to design synthesis cartridges that can be produced outside traditional manufacturing regimes, we have exploited our group’s development of 3D printed reactors—reactionware—for synthetic chemical applications as a method of prototyping the physical reactors (28, 29). Three-dimensional printing–based fabrication approaches have the added advantage of being intimately linked to the design process.

Fabrication of the modular system was carried out on low-cost (~$2000) 3D printers, Ultimaker 2 and 2+, although many other fused deposition modeling (FDM) printers could print the 3D modules produced through this approach. If it is necessary to incorporate nonprinted materials during 3D printing of the final module, a preprogrammed pause in the printing process is instigated at a point just above the designed void, and the component is inserted in this space before the resumption of printing. Upon completion of printing, the inlet and outlet ports were tapped with a ¼ inch unified national fine (UNF) thread to allow ease of integration with the external infrastructure for performing the reaction sequences. Using standard ports allowed us to attach either standard fluidic tubing connectors such as those found in traditional flow synthesis setups, or widely used Luer lock adapters. These Luer lock connectors are easily reconfigurable, facilitating feedback into the design process.

The API chosen to accomplish a complete end-to-end synthesis was the central nervous system depressant and antispastic medication (±)-baclofen (30, 31) [RS-β-(4-chlorophenyl)-γ-aminobutyric acid] (4) (Fig. 4), a derivative of γ-aminobutyric acid (GABA) that modulates the action of this central inhibitory neurotransmitter (25). This target was chosen as an example to demonstrate that even relatively short syntheses require a disproportionately larger set of chemical processing steps to effect the full synthesis; in the future, we envision that the synthesis of larger numbers of compounds and compound classes will greatly expand the scope of this approach. (±)-Baclofen has found a number of applications since its first reported synthesis and is currently being investigated beyond its traditional use, as a high-dose treatment for alcoholism (32). Many syntheses of (±)-baclofen have been published since it was first reported, often proceeding through the formation, and subsequent hydrolysis, of β-(4-chlorophenyl)-γ-butyrolactam (3). We have modified such a traditional synthesis of (±)-baclofen starting from the commercially available material methyl 4-chloro-cinammate (1), and proceeding via the Michael addition of nitromethane to form 4-nitro-3-(4-chlorophenyl)butanoic acid (2), followed by nickel-catalyzed reductive lactamization and subsequent acid hydrolysis to produce the final product in its commercially available racemic form as a hydrochloride salt. This three–reaction-step sequence contains 12 individual processing steps that must be incorporated into the reactionware device to complete the synthesis (Fig. 4). This sequence was designed to be particularly amenable to translation into the modular or monolithic system as at each stage, the reactions are either sufficiently clean, or reaction impurities that would impinge on subsequent process in the synthesis could be readily removed by phase partition. The final product is purified through a methanol–diethyl ether crystallization, which yields a crystalline solid that can be retrieved directly from the cartridge device. An animation of the entire process, showing the passage of reagents, processes, and work-ups, is shown in movie S1.

Fig. 4 Synthesis of (±)-baclofen in a series reaction cartridges.

(Top) Conceptual synthetic procedure for the synthesis of (±)-baclofen under the conditions described in Fig. 2, showing the necessary processing sequence to effect this synthetic pathway. These processes were then split into modules (a) to (e) (indicated by gray boxes in the process sequences), which we translated into a digital design (middle left) and finally fabricated as either a modular (middle right) or monolithic (bottom left) implementation. A partially fabricated monolithic cartridge is also shown indicating the placement of non-3D printed components and internal fluidic pathways (bottom center and right). Both modular and monolithic cartridges are shown with Luer taper–compatible valving for interfacing with external fluidic inputs and pressure or vacuum lines.

Each of these processes was translated into operations that could be successfully embodied in one or more reaction or purification modules. The specific reaction modules used for the synthesis of (±)-baclofen were (a) a combined Michael addition, evaporation and ether extraction module; (b) a combined solvent exchange and reduction module; (c) a phase separation and filtration module; (d) a combined solvent exchange and hydrolysis module; and (e) a filtration module. Individual modules were fabricated for a “plug-and-play” approach to the reaction process development by using Luer lock fittings to connect individual modules and Luer taper–compatible valves to interface with pressure or vacuum systems. This design allowed testing of each individual process in isolation before the modules were combined to build up the full synthesis. Finally, the module designs were “digitally stitched together” by using the developed CAD libraries for internal fluidic pathways to create the design for a monolithic synthesis cartridge. Once fabricated, the individual modules and the monolithic cartridges were evacuated and filled with a nitrogen atmosphere to ensure an inert environment for the subsequent chemistry.

The first chamber, (a), consists of a lower volume (4.9 ml) where the initial reaction can take place and is separated from the upper outlet by a hydrophobic frit. Reactor modules (b) and (d) consist of a single unbroken reaction chamber (31.8 ml) with sufficient volume to accommodate the reaction volumes and extraction solvents from the previous processes before concentration under reduced pressure. Extraction module (c) consists of a chamber of sufficient volume (4.7 ml) to contain the aqueous phase from the previous chamber, which has a drain at the bottom covered by a hydrophobic frit that prevents both solid material and aqueous solution from passing into the next chamber or module. The final module is a filtration module for separating and retrieving the final product. This single module can be either open to the atmosphere or enclosed as required. During the fabrication process, chambers or modules that required stirring were equipped with a PTFE (polytetrafluoroethylene)–coated magnetic stirring bead (length 10 mm) to enable mixing of the contents. Each module or chamber of the monolith was equipped with a ¼ inch UNF threaded port carrying a female Luer lock adapter, which was used to introduce an inert (dry, N2) atmosphere, or reduced pressure, into the system. The modular system was designed such that there was a single fluidic path through the reactor; flow from one chamber into the next was induced either by pressure from excess solvent, in the case of the phase separation processes, or the introduction of nitrogen pressure difference between the relevant chambers to push the reaction mixture through an embedded channel running from the bottom of one chamber to the top of the next.

Starting materials were prepared as simple solutions and transferred to the cartridge via standard Luer syringes. The cooling and heating required for the reaction sequence were achieved by the immersion of the reaction cartridge or module in an ice or sand bath, respectively, and the temperature required for the reactions can be achieved automatically on a stirring-hotplate. The exact sequence of operations, positioning of the module in the heating or cooling bath, and time intervals necessary for completing the synthesis are outlined in the supplementary materials (figs. S12 and S13 and table S3).

Performing the synthesis starting from 200 mg of 1 in the manner described yielded 98 mg (39% yield over three reaction steps and 12 processing steps from 1 with ≥95% purity as determined by high-performance liquid chromatography) of (±)-baclofen hydrochloride salt, which is more than 1 day’s maximum dosage of the drug. Better efficiency of reaction can be achieved with lower concentrations of starting materials (using a similar cartridge at half concentration, i.e., 100-mg scale, gave a 44% yield over three steps of similar purity). Increasing the volume of the reactor as well increases the quantity of (±)-baclofen obtained [a 300-mg scale synthesis yielded 133 mg (35%) (±)-baclofen]. The integration of the reaction processing steps into the design of the modules greatly simplifies the operations required to perform the reaction sequence compared to traditional bench synthesis and simultaneously reduces the level of technical skills required to perform the process down to simple operations that do not require the specific skills of a trained synthetic chemist. Although the total time for the reaction sequence is around 40 hours in this case, including all intermediate operations, the workflow is constrained by the geometry of the device, so all human interaction is limited to simple interventions at specific time periods, and it should be possible to shorten the interaction time further. The use of such bespoke, single-use cartridges would greatly reduce the time spent on glassware preparation, liquid handling, and other ancillary tasks associated with the majority of chemical syntheses at this scale. Also, by using the geometry of the reactor to constrain the operation of the synthesis, we reduce the human decision making involved in the synthesis processes, making the sequence more reproducible. Given sufficient facilities, several instances of the synthesis cartridge could be used at once, achieving scalability by numbering-up arrays of cartridges, and using these in parallel to increase the output. As a result of the ability to parameterize and encode multistep organic synthesis reactions with work-ups embedded, we envisage that a digital programmable universal heater-stirrer-solvent-reagent plug-and-play device can be constructed into which only the cartridge, specific to a given synthesis, can be plugged in.

The (±)-baclofen synthesis necessitated liquid handling and separation of reaction chambers to effect the full reaction sequence. In some cases, however, syntheses can be conducted in single reaction cartridges, depending on the nature and quality of the interstep purification required. For example, the synthesis of lamotrigine (Fig. 2) can be achieved in a single cartridge as the intermediate material is insoluble in the reaction solvent at low temperatures. In a single, closed, filtration module, the initial reaction product could be washed and processed in situ before introduction of the solvent for the subsequent cyclization step. This stands in contrast to the traditional procedure, which requires the solid product of the first step to be removed from the initial reactor to be filtered, dried, and then reintroduced to a reactor for the second step of the synthesis. Performing the synthesis of lamotrigine on a 250-mg scale of starting material yields 112 mg (46% over two reaction steps) of the final product, giving an off-white crystalline powder.

The digital approach to the design of the system that we have adopted allows the blueprints for these cartridges to be stored electronically for implementation as and when required. The distribution model for fine and specialty chemicals, such as the APIs implied by this approach, would lead to a decentralizing of logistical approaches to chemical manufacture. Here, any location with access to a sufficiently diverse market of chemical precursors and suitable cartridge fabrication facilities could be used to produce chemical products, which could previously be achieved only in a fully equipped synthesis laboratory with highly trained staff. This approach not only holds promise for eventually delivering on-demand personalized medicines manufactured at, or near, the point of use, but also has short-term potential applications in the synthesis of APIs that are currently out of production. An immediate impact of digitization is that the cost for synthesis at the bench scale (milligrams) could decrease markedly owing to savings in labor and infrastructure with only a one-off digitization cost (and allow operators to make 5 to 10 different products at the same time). Once the saving meets the digitization cost, the efforts of the expert chemist will shift from bespoke on-demand chemical manufacturing to chemical digitization (see supplementary materials for an economic analysis). Our methodology will have the most rapid impact for chemicals that are currently produced on demand in small batches and that occupy a gap in the market where the demand for a product is sufficient for it to be commercially viable but insufficient to justify plant-scale production. This gap lies between the high cost of bench-scale versus reactor-scale synthesis, and thus the digitization benefit of compounds in this zone is high.

The regulatory framework necessary to produce complex materials in this fashion will need thorough attention; indeed, our approach would require a completely new system for the regulation of API manufacture. This system would have to be developed alongside the evolution of this approach as a method for pharmaceutical synthesis, which we have presented here in proof-of-concept form; however, we can envision a situation in which regulatory agencies certify specific cartridge or module designs as soon as a digitized process is fully established (including the embedded quality-control protocols), independent of the physical location of person who uses the cartridge. This approach has multiple benefits. First, the framework can adopt well-established methods of digital object certification from the information technology universe (e.g., digital signing with asymmetric ciphers). Second, no explicit certification would be needed for each new “facility” (which might be a hospital or a private house) that would need the drug. Third, existing methods for protecting and manipulating digital content provide much more efficient models for distribution and regulation compared to the retail and patent system, respectively. These regulatory issues surrounding the commercial or clinical application of this approach are not trivial, and care must be taken to ensure that end-user safety is not compromised. However, we believe that the benefits in terms of efficiency of delivery, robustness of supply, and range of materials available could lead to the digitization of chemical synthesis.

Acknowledgments: We acknowledge the help of S. Marshall in compiling our analysis of the economic impact of our methodology. Supplementary materials include a PDF document detailing the materials and methods used in this article; the STL and OpenSCAD files used to generate all 3D printed objects mentioned; a schematic movie illustrating the process of baclofen synthesis in the monolithic cartridge; and Python code that can be used to automate the stirrer-hotplate operations for the baclofen synthesis. We gratefully acknowledge financial support from the Engineering and Physical Sciences Research Council (grant nos. EP/H024107/1, EP/J015156/1, EP/K021966/1, EP/L015668/1, EP/L023652/1) and European Research Council (project 670467 SMART-POM). This research was developed with funding from the Defense Advanced Research Projects Agency (DARPA). The views, opinions and/or findings expressed are those of the author and should not be interpreted as representing the official views or policies of the Department of Defense or the U.S. Government. L.C. is the founder and director of CroninGroupPLC and is listed as an inventor on a patent application filed by The University of Glasgow (GB 1800299.8). L.C. conceived the initial concept and the design approach; P.J.K. designed the reactionware with help from J.P.F. and S.Z.; G.M. and R.C.S. telescoped the methods, porting them from glass to plastic; and P.J.K. developed the monolithic cartridges with help from S.Z. J.S.M. helped evaluate the purity of the products, and P.J.K. coordinated the team with help from L.C.


Top Tutorials To Learn MATLAB For Beginners | killexams.com real questions and Pass4sure dumps

As the volume and complexity of data and results continues to grow with the increasing complexity of data sources and algorithms, the need for intuitive representations of that data and results becomes increasingly critical.

We want to create the representations in such a way that the human mind can, after all, better understanding our universe and the processes taking place within — representation of a real-world object, an abstract mathematical expression, specific values of some measurable quantities, etc. Since 80 percent of the sensory information the brain receives comes from our eyes, the visual presentation of data is the natural choice.

The graphical representation of the results is often not only the most effective means of conveying the points of the study or work which has provided the data, but is in most cases an expectation of the audience of the work. It helps you to identify and emphasize areas of interest in data behavior, to express your thoughts, observations, and conclusions to others in a quick and intuitive way.

Why MATLAB?

1. Ease of Use

MATLAB is an interpreted language. Programs may be easily written and modified with the built-in integrated development environment and debugger.

2. Platform Independence

MATLAB is supported on many different computer systems, providing a large measure of platform independence. The language is supported on Windows, Linux, Unix, Macintosh. Programs written on any platform will run on all of the other platforms.

4. Device-Independent Plotting

MATLAB, unlike other computer languages, has many integral plotting and imaging commands. The plots and images can be displayed on any graphical output device supported by the computer on which MATLAB is running. This capability makes MATLAB an outstanding tool for visualizing data.

5. Full set capabilities

MATLAB has all graphics functions necessary to visualize scientific and engineering data. It includes features for representation of two-dimensional and three-dimensional diagrams, three-dimensional volume visualization, animation, tools to create diagrams interactively and the possibility of exporting to the most popular graphic formats. It is possible to customize diagrams adding multi-axes, change the colors of the lines and markers, add annotations, LaTeX expressions, legends and other plotting options.

1. Become a Good Matlab Programmer in less than 30 days

This is the last time, you wish you could be a Matlab Programmer.

Matlab Programming is one of the most important technical programming languages and skills today. In this course, we will start learning Matlab from beginner level, and slowly we ease our way into more technical topics. This course is a general Matlab Programming, and it means that all the majors can benefit from this course. Matlab Programming is an easy and understandable programming language and is an excellent choice for learning before starting other programs like Java, Python, C, and C++.

The list of contents is:

Chapter 1: An Introduction to Matlab Software

Chapter 2: Mathematics in Matlab

Chapter 3: Working with Variables in Matlab environment

Chapter 4: Trigonometric Functions in Matlab

Chapter 5: Complex Numbers in Matlab

Chapter 6: Working with Vectors in Matlab

Chapter 7: Working with Matrices in Matlab

Chapter 8: Introduction to Calculus and Engineering Functions in Matlab

Chapter 9: Graphs and Plotting in Matlab

Chapter 10: Loops, Conditions, and Intro to Programming in Matlab

Chapter 11: Projects (Updates Weekly with new programming drills)

Chapter 12: Import Data from Excel to Matlab

Chapter 13: How to Claim your Coursovie Training Certificate (LinkedIn)

Chapter 14: Bonus Materials for the Course

Chapter 15: Massive Discount Codes for other Courses (Coursovie Collection)

Find the best free online courses to learn MatLab and other programming languages on Quick Code.

Get new updates on new free courses on Facebook Messenger.

2. Complete MATLAB Tutorial: Go from Beginner to Pro

Essential MATLAB Tutorial that will take you from beginner to advance level.

MATLAB (matrix laboratory) is a multi-paradigm numerical computing environment and fourth-generation programming language which is frequenlty being used by engineering and science students. In this course, we will start learning MATLAB from a beginner level, and will gradually move into more technical and advnace topics. This course is designed to be general in scope which means that it will be beneficial to students in any major. Once, passed a certain learning thresholds, you will definately enjoy MATLAB Programming. The key benefit of MATLAB is that it makes the programming available to everyone and is very fast to turn ideas into working products compared to some of the conventional programming languages such as Java, C, C++, visual basic and others.

Below is the detailed outline of this course.

Segment 1: Instructor and Course Introduction

Segment 2: Handling variables and Creating Scripts

Segment 3: Doing Basic Maths in MATLAB

Segment 4: Operations on Matrices

Segment 5: Advance Math Functions with Symbolic Data Type

Segment 6: Interacting with MATLAB and Graphics

Segment 7: Importing Data into MATLAB

Segment 8: File Handling and Text Processing

Segment 9: MATLAB Programming

Segment 10: Sharing Your MATLAB Results

Segment 11: Cell Data Type

Segment 12: Tables and Time Tables

Segment 13: Working with Structures and Map Container Data Type

Segment 14: Converting between Different Data Types

3. Learn MATLAB and Simulink Programming

Master MATLAB Programming fundamentals and Simulink to increase your number crunching abilities.

Learn MATLAB and Simulink Programming is a course that focuses on teaching students about the various commands, functions, and features that MATLAB and Simulink have to offer. MATLAB and Simulink have a lot of capabilities and so this course will only focus on the main topics to get you comfortable creating your own scripts and Simulink models. This course contains many examples of different projects as well as step-by-step solutions to help you best understand what is going on. the completed code is attached in the projects so that students can download and get the same results they see onscreen.

This course is designed to teach students through a combination of articles to help explain various topics and videos to show examples of these topics. There are also various quizzes that are designed to test students and let them know if they sufficiently understand the information presented in the section. This course starts out by briefly covering an overview of the MATLAB environment and where specific tools are located. Each section of this course covers different topics including the following:

  • Generating Figures
  • Plotting Data
  • Basic MATLAB Commands
  • Vectors
  • Matrices and Matrix Commands
  • MATLAB Scripts
  • Programmings Loops & Conditional Statements
  • User Defined Functions
  • Simulink
  • Simulink Features
  • Example Simulink Projects
  • There are several quizzes that will test your understanding of the various sections. There are multiple projects that require students to solve problems using MATLAB & Simulink.

    Each of the projects in this course contain the following information:

    Instructions: This article explains what is required to complete the project.

    Demonstration: This lecture demonstrates what is expected of the students in terms of how to complete the project.

    Step-By-Step Solution: This lecture explains the thought process and how to complete the project in a step-by-step fashion.

    4. Learn MATLAB programming, debugging, and style

    Learn the key MATLAB programming skills that separate experts from novices: debugging, functions, and visualization.

    MATLAB is one of the most important and widely used programming environments, data visualization tools, and numerical solvers in academia and industry. On the other hand, MATLAB is just a programming language, not so different from learning other “high-level” coding or visualization languages; therefore, my goal in this course is not just to teach you how to code in MATLAB, it’s to teach you high-level, transferable skills that will help you become a better programmer, regardless of whether you are using MATLAB, Python, R, JavaScript, or any other language.

    What you will learn in this course:

  • Using and customizing the visual MATLAB environment (including replacing those awful default black-on-white colors with something that suits your colorful personality!)
  • MATLAB programming basics
  • Control statements (for-loops, while, if-else, switch)
  • Make your own MATLAB functions
  • Create and edit data visualizations using the MATLAB graphics engine
  • How to write good, clean, readable code
  • General strategies for debugging (finding and fixing errors)
  • Recognize common coding mistakes and how to avoid them
  • How to organize and optimize your code before you start coding
  • Build confidence about your programming skills
  • 5. Data Visualization with MATLAB — Projects and Examples

    Learn how to Visualize Data with MATLAB in 2D, 3D, 4D, 5D and create animated plots with tens of projects and examples.

    Why this course?

  • Breaks the complex plot techniques down into simplistic steps.
  • Easy and intuitive approach from professional trainers.
  • Ideal for students, academics, scientists.
  • Suitable for beginner programmers.
  • 6. Learn Matlab Programming by Examples (Codes Included)

    An Intermediate & advanced guide for getting proficiency in Matlab Programming Fast.

    The list of contents is:

    Chapter 1: General & Important Notes

    Chapter 2: M-Files, Functions, and Scripts in Matlab

    Chapter 3: Matrices and Vectors

    Chapter 4: Importing and Exporting Files in Matlab

    Chapter 5: Decision Making Techniques in Matlab

    Chapter 6: Strings & Text Manipulation

    Chapter 7: Plotting & New Features

    Chapter 8: Matlab Programming Techniques

    Chapter 9: References and Conclusion

    7. MATLAB Basics for Beginners

    Learn MATLAB Programming with step by step Exercises.

    This is a practicing course for MATLAB. Learn the leading software in numerical computing through step by step exercises. Master the basics and move to an advanced level in MATLAB.

    MATLAB is a leading software in numerical computing and building algorithms that is widely used by Engineers, Programmers, Researchers, Teachers, Colleges and Entrepreneurs.

    In this course you will start learning MATLAB by creating and manipulating Matrices which are the key for MATLAB programming, then you will learn how to use MATLAB in some Elementary Mathematics Problems, after that comes the Graphics section in which you will learn how to use MATLAB to produce 2D & 3D graphs also how to build 2D animations. In the programming section you will learn how to use MATLAB as a programming language to build your own Algorithms, you will learn how to import and analyze data to MATLAB, and finally you will get introduced to the symbolic capabilities of MATLAB.

    8. Learn MATLAB with Image Processing from scratch!

    Learn how to use MATLAB with this awesome toolbox of Image Processing. No previous experience required at all.

    MATLAB’s Image Processing (IP) toolbox is insanely popular and widely used in almost all academic Institutions and Enterprises. That’s because, it is so well written and organized, that it makes this toolbox very user-friendly for even the toughest of the IP operations.

    If you want to learn MATLAB for your Work or College, this is the right course for you. This course teaches you this complete Image Processing toolbox from scratch. All the theoretical concepts have been explained in presentations with examples. Then, their implementation is covered with Matlab Programming. All these presentation files and working Matlab scripts are provided as supplementary materials along with the lectures. You don’t need any previous Matlab Programming experience to take this course, as it starts everything from scratch.

    The course content covers all the (Beginner and Intermediate Level) topics in IP toolbox like Image Filtering, Noise Removal, Morphological Operations, Histogram operations, Image Thresholding, Edge Detection and basics of Image Segmentation. Several quizzes have been set up to keep a track of your performance and understanding. Besides all the theoretical content, some real world applications have been covered as well in the form of Projects Like “Detect the faces of all your friends in an image”

    9. MATLAB for Scientists and Engineers

    Introduction to MATLAB for Engineers and Scientists.

    Whether of engineering, science, economics or medical background, you are about to join over 2 million users of MATLAB that cut across these backgrounds; a multi-paradigm numerical computing environment and fourth-generation programming language that allows matrix manipulations, plotting of functions and data, implementation of algorithms, creation of user interfaces, and interfacing with programs written in other languages, including C, C++, C#, Java, Fortran and Python with additional package, Simulink, adds graphical multi-domain simulation and model-based design for dynamic and embedded systems.

    This course starts from the elementary topics, then progressively and systematically advances to more advanced (but well explained) topics in MATLAB. It touches the major topics Engineers and Scientists meet on daily bases and major aspects of MATLAB you need to progress to become an expert. After this course, you can stand boldly and tackle those difficult problems on your own with MATLAB and be able to proceed and specialize on any aspect of MATLAB you choose to.

    Each lecture has quiz which must be attempted to obtain a certificate for this course. Each section has assignment which can be evaluated by fellow Udemy students if you give the permission. Note that some of these quizzes serve as summary to the course, you will get to learn some more things and also understand some key facts emphasized in the lectures. The step-by-step answers to the assignment are also provided.

    In this course, you will typically become a guru and will move from zero knowledge in MATLAB to hero.

    10. MATLAB Projects with iPhone & iOS Sensors

    Build your own MATLAB programs using the Accelerometer, Compass, GPS & other iOS Sensors on your iPhone & iPad.

    Now you can collect sensor data from your iPhone or Apple iOS device using MATLAB! Impress your friends, build some cool programs, and take your MATLAB skills to a new level with this interactive course. You’ll learn how to capture and utilize data from 5 different sensors without the need to buy additional software or hardware.

    Build 6 iPhone Sensor Projects (Source Code Included)

    In this course, you will master the MATLAB® Support Package for Apple iOS Sensors by building a unique set of projects which enable you to:

  • Build Your Own 3D Compass
  • Rotate 3D Objects Using Your Phone
  • Detect iPhone Facing Up or Down
  • Track Position and Speed of A Car
  • Detect Shaking
  • Count Your Steps While Walking
  • Getting set up is a little tricky, but, don’t worry, I’ll walk you through it. And if you have any problems you can ask for help through the discussion forum. I’ll show an easy method to enable and acquire data from all 5 iOS sensors including:

  • Acceleration Sensors — Learn how to use abrupt changes in your iPhone’s movement
  • Magnetic Field Sensors — Explore magnetic fields used by the compass and other input devices
  • Orientation Sensors — See how you can detect your iPhone state and control virtual items
  • Angular Velocity Sensors — Detect your iPhone’s movement and use to control software
  • Position Sensors — Capture your GPS position and speed and build location based apps
  • You will learn how easy it is to enable these sensors and acquire data for your MATLAB programs.

    Be a part of Quick Code Community to receive special offers on free and paid courses before everyone else.😍

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    Late Preterm Infants and Neurodevelopmental Outcomes at Kindergarten | killexams.com real questions and Pass4sure dumps

    Late Preterm Infants and Neurodevelopmental Outcomes at Kindergarten | Articles | Pediatrics

    '); document.write(''); } function OAS_AD(pos) { if (OAS_version >= 11 && typeof(OAS_RICH)!='undefined') { OAS_RICH(pos); } else { OAS_NORMAL(pos); } } //-->



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