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International Conference on Pharmaceutical Analysis, Drug Discovery and Designing Chemistry, will be organized around the theme “Analytical Techniques for Analysis of Pharmaceutical Products”

Pharmaceutical Analysis 2018 is comprised of 15 tracks and 85 sessions designed to offer comprehensive sessions that address current issues in Pharmaceutical Analysis 2018.

Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.

Register now for the conference by choosing an appropriate package suitable to you.

Of late there is a marked interest in enhancing the approaches for analytical method development, validation, and lifecycle management. Most of these are aligned to Quality by Design (QbD) approach for drug development. The enhanced approaches mostly utilize risk assessments and in-depth systematic evaluations of critical method variables to identify the controls required to ensure that the measurement uncertainty of a reportable result is controlled to a level that ensures that the method is “fit for purpose”. Traditional subjective methods use partitions, for example, precipitation, extraction, and distillation. ID might be founded on contrasts in color, odor, melting point, boiling point, radioactivity or reactivity. Established quantitative analysis uses mass or volume changes to measure sum.

  • Track 1-1Physical Analytical Methods
  • Track 1-2Titrimetric Methods
  • Track 1-3Specific methods
  • Track 1-4Reagents
  • Track 1-5Miscellaneous Methods

It is the process to discover a new drug and bringing a drug to the market once a lead compound has been identified through the process of drug discovery. It includes pre-clinical research on microorganisms and animals, filing for regulatory status, such as via the United States Food and Drug Administration and present day logical strategies including the use of refined instruments like GC, HPLC, NMR, GC-MS, and LC-MS and so on for medications, pharmaceuticals and others for an investigational new drug to initiate clinical trials on humans, and may include the step of obtaining regulatory approval with a new drug application to market the drug.

 

  • Track 2-1Random screening
  • Track 2-2Molecular manipulation
  • Track 2-3Molecular metabolites
  • Track 2-4Drug metabolites
  • Track 2-5Industrial pharmacy

Analytic method development and validation are persistent and interconnected exercises directed all through the drug development process. The act of validation checks that a given method measures a parameter as planned and sets up the execution furthest reaches of the estimation. Albeit clearly conflicting, approved methods create comes about inside known vulnerabilities. These outcomes are essential to proceeding with drug development, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing logically solid, hearty, and transferrable analytic methods ought to be lined up with the drug development arrange. The assets that are consumed on method validation must be constantly balanced with regulatory requirements and the likelihood for product commercialization.

  • Track 3-1Classical Methods
  • Track 3-2Instrumental Methods
  • Track 3-3Standards & Errors in Analytical methods
  • Track 3-4Calibration methods for pharmaceutical analysis

Generally, pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may, throughout the years, present day pharmaceutical investigation has advanced past this to envelop mix systems, high-throughput innovations, chemo metrics, micro dosing studies, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosure and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new, enhanced and advancing innovations, and in addition new applications for existing innovation, the scan for new medications for the aversion and treatment of human maladies proceeds.

  • Track 4-1Documentation of pharma industry
  • Track 4-2Regulation of the quality of analytical methods
  • Track 4-3Biological respond and chemical purity thermo analytical analysis
  • Track 4-4High performance liquid chromatography

Chromatography strategy for isolating the parts, or solutes, of a blend on the premise of the relative measures of every solute appropriated between a moving liquid streams, called the versatile stage, and a touching stationary stage. The versatile stage might be either a fluid or a gas, while the stationary stage is either a strong or a liquid. Kinetic sub-atomic movement persistently trades solute particles between the two stages. On the off chance that, for a specific solute, the circulation supports the moving liquid, the atoms will invest a large portion of their energy relocating with the stream and will be transported far from different species whose particles are held longer by the stationary stage. For a given animal types, the proportion of the circumstances spent in the mobile and stationary areas is equivalent to the proportion of its focuses in these locales, known as the partition coefficient. (The term adsorption isotherm is regularly utilized when a strong stage is included).

  • Track 5-1Adsorption chromatography
  • Track 5-2Partition chromatography
  • Track 5-3Ion exchange chromatography
  • Track 5-4Separation techniques in chemistry
  • Track 5-5Affinity chromatography
  • Track 5-6Gas chromatography
  • Track 5-7Special techniques in chromatography
  • Track 5-8Advancement and application in chromatography
  • Track 5-9Novel techniques in chromatography

Quality control, or QC for short, is a procedure by which elements audit the quality of all elements engaged with creation. ISO 9000 characterizes quality control as "A piece of quality administration concentrated on satisfying quality necessities". Components, for example, controls, work administration, characterized and all around oversaw procedures, execution and respectability criteria, and recognizable proof of records Competence, for example, knowledge, skills, experience, and capabilities. Delicate components, such as personnel, integrity, confidence, organizational culture, motivation, team spirit, and quality relationships. Controls incorporate item assessment, where each item is inspected outwardly, and frequently utilizing a stereo magnifying instrument for fine detail before the item is sold into the outside market. Examiners will be furnished with records and depictions of unsuitable item deformities, for example, breaks or surface flaws for instance. The quality of the yields is in danger if any of these three angles is insufficient in any capacity.

  • Track 6-1Control of errors in analysis
  • Track 6-2Accuracy & Precision
  • Track 6-3Validation of analytical procedures
  • Track 6-4Compound random errors
  • Track 6-5Basic calculations in pharmaceutical analysis

Analytical errors are fundamental before submitting your report and results with the required level of confidence. However, we should have clarity regarding accuracy and precision before we are talking pharmaceutical error. Most of us believe that these terms have the same meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique and the skill of the observer. Where a measurement consists of a single reading on a simple piece of laboratory equipment, for example, a burette or a thermometer, one would expect the quantity of factors adding to vulnerabilities in that estimation to be less than an estimation which is the consequence of a multi-step process comprising of at least two weight estimations, a titration and the utilization of an variety of reagents.

 

  • Track 7-1Statistical validation
  • Track 7-2Classification of errors

Electroanalytical method is used to determine the concentration of a chemical compound or chemical element with their high sensitivity and appropriateness for measuring redox reactions, electroanalytical methods are ideal fdor pharmaceutical analysis. 

  • Track 8-1Electrogravimetry
  • Track 8-2Conductometry
  • Track 8-3Coulometry
  • Track 8-4Potentiometry
  • Track 8-5Voltammetry

These Drugs often produce adverse effects in different tissues and organ systems. Redox homeostasis is essential for cell health and survival and oxidative stress has been proposed as a key mechanism behind drug-induced adverse effects.

 

  • Track 9-1Analysis of Barbiturates
  • Track 9-2Analysis of Diuretics
  • Track 9-3Analysis of Antibiotics
  • Track 9-4Analysis of Alkaloids drugs
  • Track 9-5Analysis of Steroids
  • Track 9-6Analysis of Local Anaesthetic drugs
  • Track 9-7Analysis of Anti- Pyretics & Analgesics

Good manufacturing practice is the piece of quality assurance which ensures that things are reliably made and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stressed over both generation and quality control, consistency with this standard gives open assurance that the rights, security, and prosperity of trial subjects are ensured; predictable with the rule that have their starting point in the Declaration of Helsinki, and that the clinical information is valid.

 

  • Track 10-1Guideline versions
  • Track 10-2High-Level details
  • Track 10-3Enforcement
  • Track 10-4CGMP inspections
  • Track 10-5Controlled environmental conditions

Analytical biochemistry is the study of biochemical components found in a cell or other biological sample. This field uses a broad vary of techniques for separation, identification, quantification and practical characterization of biological molecules like nucleic acids, enzymes, proteins, pigments, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biological components are qualitative analysis techniques, chromate graphical Techniques, super molecule Estimation & Purification Techniques and medicine Techniques.

  • Track 11-1Membrane technology in separation processes
  • Track 11-2Novel separation techniques in chemistry
  • Track 11-3Emerging separation technologies
  • Track 11-4Biological Techniques
  • Track 11-5Biochemical Components

Modern microbiology is unmistakably a branch of biotechnology and incorporates the customary and nucleic corrosive aspects. Pharmaceutical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straightforwardly or with the utilization of some item delivered by them.  

  • Track 12-1Microorganisms
  • Track 12-2Exotoxin and Endotoxin
  • Track 12-3Validation of Disinfectants
  • Track 12-4Antimicrobial Activity and Disinfection
  • Track 12-5Sterile Products

New innovations for example those that give better approaches to target therapeutic items to particular destinations inside the body or to control hereditary material. The division is associated with showing pharmaceutical investigation to the students. The educational programs incorporate broad addresses and research facility sessions to guarantee that understudies can interface hypothesis to rehearse and apply their hypothetical information picked up. The field of pharmaceutical examination is extremely powerful and the educational modules guarantees that the understudies are stayed informed concerning the most recent improvement in this field. They are shown traditional and present day logical strategies including the use of refined instruments like GC, HPLC, NMR, GC-MS, and LC-MS and so on for medications, pharmaceuticals and others.

  • Track 13-1Analytical Techniques and Instruments for Preformulation Studies
  • Track 13-2Thermal Analytical Methods
  • Track 13-3Separation Sciences
  • Track 13-4Specific Detection

The discovery and development of new solutions is a long, complex and rigorous process. Each progression is gone for conveying compelling pharmaceuticals to patients as fast as could reasonably be expected, while guaranteeing the most noteworthy conceivable level of wellbeing. It takes a normal of ten years to build up a potential new prescription. Advances in our understanding of human science and malady are opening up energizing new conceivable outcomes for potential new medications and cures to address persistent issues. As the complexity of the science increments and R&D challenges mount, researchers are ceaselessly adjusting and improving to speed restorative advances. Researchers are working each day in labs over the U.S. and around the globe to transform logical guarantee into new drugs for patients. Research-based biopharmaceutical organizations are focused on propelling science and creating imaginative drugs. Understanding the guarantee and potential of the pipeline will require expanded joint effort and merging over a scope of segments and fields to outfit novel logical methodologies, enormous measures of information and computational capabilities, and a scope of new advancements. The extent of logical and mechanical difficulties and openings are proclaiming another period of communitarian movement over a scope of partners. Guaranteeing an ideal strategy and administrative condition is basic to supporting the lively life sciences biological community in the U.S. and encouraging the development of new medicinal advances against our most expensive and testing infections.

  • Track 14-1Biological Molecules
  • Track 14-2Drug Metabolism
  • Track 14-3Biological respond and chemical purity Thermo analytical analysis
  • Track 14-4Pharmacokinetics
  • Track 14-5Clinical Trials Process

Nanotechnology has turned into a fundamental component of pharmaceutical sciences and finds various applications in sedate conveyance frameworks in upgrading remedial execution of medications. A considerable lot of the current "Nano" medicate conveyance frameworks are family of traditional measurements shapes like Nano suspensions, Nano emulsions and Nano micelles. Nano suspension is a way to deal with conveys water insoluble and inadequately bioavailable medications by decreasing size to submicron extend. Along these lines its disintegration rate is expanded and thus the bioavailability, where tranquilize disintegration rate is the constraining element. Nano emulsions are O/W or W/O emulsion, having bead measure from 20-200 nm that are straightforward and don't tend to mix. Nano emulsions demonstrate awesome stylish interest and skin feel and discover their application in transdermal conveyance of medications, topical application for foundational sedate conveyance, oral conveyance of proteins and conveying drugs through parenteral and intranasal courses.

 

  • Track 15-1Biological evaluation
  • Track 15-2Drug targeting and design
  • Track 15-3Clinical testing
  • Track 15-4Smart drug delivery Systems
  • Track 15-5Biomaterials in drug delivery
  • Track 15-6Toxicological assessment of nanomaterial
  • Track 15-7Pharmaceutical innovation
  • Track 15-8Drug synthesis