Theme: Analytical Techniques for Analysis of Pharmaceutical Products

Pharmaceutical Analysis 2018

Pharmaceutical Analysis 2018

Conference Series LLC Ltd invites all the participants from all over the world to attend “International Conference on Pharmaceutical Analysis and Quality Control Strategies” one of its remarkable Pharmaceutical conferences, to be held during June 27-28, 2018 in Vancouver, Canada. This Pharmaceutical Analysis 2018 Conference includes a wide range of Keynote presentations, Oral talks, Poster presentations, Symposia, Workshops, Exhibitions and Career development programs.

Why to attend???

The Pharmaceutical Analysis 2018 anticipates participants, renowned speakers and eminent delegates across the globe to be attending the conference to share their valuable presentation and galvanize the scientific community. Scientific people from all over the globe focused on learning about emerging technologies about Pharmaceutical Analysis. This is a best globalized opportunity to reach the largest assemblage of participants from the scientific community and research.

This  Pharmaceutical Analysis 2018 emphasizing on recent areas of more optimized research techniques like experimental design, Chemo metrics, chromatography, electrophoresis, Qualitative and Quantitative analysis and also in forensics, medicine, science and engineering.

Conduct presentations, distribute information, meet with current and potential scientists, make a splash with new drug research developments, and receive name recognition at this 2-days event. World renowned speakers and the most recent techniques, developments, the newest updates in Pharmaceutical Analysis are hallmarks of this conference.

Target Audience:

Our Organization would be privileged to welcome the:

  • Pharmaceutical Researchers
  • Pharmaceutical Industry Professionals (CEOs, MDs, Directors)
  • Academicians (Professors, Deans, Directors,)
  • Pharmaceutical Associations and Societies
  • Young Researchers and Students
  • Post -Doctoral

Track 1: Analytical Method Development and Validation

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 2: Drug Discovery & Development

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 3: Analytical Methods and Control Strategies

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 4: Modern 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 5: Chromatography & Separation Techniques

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 6: Quality Control of Analytical Methods

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 7: Errors in Pharmaceutical Analysis & Statistical Validation

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 8: Electroanalytical Methods

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, electro analytical methods are ideal FDOR pharmaceutical analysis.

Track 9: Analysis of Pharmaceutical Agents

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 10: GLP and GMP Method Development, Validation and Remediation

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 11: Pharmaceutical and Biomedical Analysis

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 12: Pharmaceutical Microbiology

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 13: Preformulation Studies

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 14: Biopharmaceutical Research & Development Process

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.

Track 15: Pharmaceutical Nanotechnology

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.

 

International Conference on Pharmaceutical Analysis which is going to held during June 27-28, at Vancouver, Canada. Gathering all the renowned Speakers, Scientists, Academicians, Students, and Business Tycoons at a Common Scientific Platform to discuss, Developed, and discover the advancements in the arena of pharmaceutical Analysis and Quality Control Strategies.

Theme: Analytical Techniques for Analysis of Pharmaceutical Products

The global pharmaceutical excipients market is projected to reach USD 3.35 Billion in 2021 at a CAGR of 18.2% in the forecast period 2016 to 2021. The rising demand for new drug delivery systems, greater understanding of the functional benefits of excipients, growing pharmaceutical industry, and patent expiries of several blockbuster drugs are positively impacting the overall growth of the market. The global particle size analysis market over the forecast period of 2017 to 2021. The market is expected to reach USD 256.1 Million by 2021, at CAGR of 4.7% from 2017 to 2021. Increasing nanotechnology research, presence of stringent regulatory guidelines to ensure compliance with GMP guidelines, and growing efforts by players to expand their geographic presence are driving the growth of the particle size analysis market during the forecast period. Analysis software market is expected to reach USD 3,135.3 Million by 2020 from USD 2,143.7 Million in 2017, at a CAGR of 7.9% from 2017 to 2020.

The survey by the Global Industry Analysts announced the release of a comprehensive global report on chromatography systems market. The global market for chromatography systems, pharmaceutical analytical techniques for the study and research is forecast to reach $1.4 billion by the year 2015.The global market of Pharmaceutical Analysis is forecasted to be around $3.4 billion by 2019, growing at an approximate CAGR of 13% in the forecasted years. America has the largest market growth followed by Asia-Pacific and Europe. The Pharmaceutical Analysis and biotechnology market is poised to grow at a CAGR of around 14% over the next decade to reach approximately $9 billion by 2025.

For conference attendance and participation only Business Visa should be applied. Contact your nearest travel agent/visa information center/US Embassy for the correct application form.

All visas for visiting US shall be processed by respective authorities only upon submission of proper documents through proper channel.

In case of non-furnishing of documents, non-adherence to guidelines visas shall be cancelled by respective authorities.

The minimum supportive documents that might be required while applying for US visa include:

Letter of invitation,

Abstract acceptance letter (if speaker),

Registration payment receipt,

Accommodation confirmation letter issued under conference letter head.

For letter of invitation and accommodation confirmation, payment of registration fees and accommodation charges is a pre-requisite.

Mandate documents required from conference secretariat should be obtained only through Alina Jasmine or Will Thomas.

For more details please contact

Alina Jasmine

Program Manager

Pharmaceutical Analysis 2018

E: [email protected]

T: +1-702-508-5200

 

Pharmaceutical Analysis 2018

Pharmaceutical Analysis 2018 Report:

Conference Series LLC Ltd successfully hosted the International Conference on Pharmaceutical Analysis and Quality Control Strategies during June 27-28, 2018 at Vancouver, Canada. The conference focused on the theme “Analytical Techniques for Analysis of Pharmaceutical Products”. The conference was successful in gathering eminent speakers from various reputed organizations and their paramount talks enlightened the gathering.

The pragmatic meet organized by Conference Series LLC Ltd received generous response from the Editorial Board Members of Journals as well as expertise from academia, talented researchers and young student community. Researchers and students who attended from different parts of the world made the conference one of the most successful events in 2018 from Conference Series Group. The conference was marked with the presence of renowned Speakers, Young Researchers, Students and Business Delegates driving the two day event into the path of success with thought provoking keynote and plenary presentations.

Pharmaceutical Analysis 2018 is designed to offer comprehensive range of sessions that includes Drug Discovery and Development, Analytical Methods and Control Strategies, Pharmaceutical Nanotechnology and many more

  1. Analytical Methods and Control Strategies
  2. Drug Discovery & Development
  3. Analytical Method Development and Validation
  4. Modern Pharmaceutical Analysis
  5. Chromatography & Separation Techniques
  6. Quality Control of Analytical Methods
  7. Errors in pharmaceutical analysis & statistical validation
  8. Electroanalytical Methods
  9. Analysis of Pharmaceutical Agents
  10. GLP and GMP Method Development, Validation and Remediation
  11. Pharmaceutical and Biomedical Analysis
  12. Pharmaceutical Microbiology
  13. Preformulation Studies
  14. Biopharmaceutical Research & Development Process
  15. Pharmaceutical Nanotechnology

The proceedings of the conference were embarked with an Opening Ceremony followed by a series of Lectures delivered by both Honourable Guests and members of the Keynote forum. The adepts who promulgated the theme with their exquisite talks were:

  1. Steinar Madsen - Medical Director, Norwegian Medicines Agency
  2. Steven J. Durham - Partner  Labaton Sucharow, USA
  3. Kouros Motamed - Director Drug Development, NantBioscience Inc , USA
  4. Yara Peluso Cid, Federal Rural University of Rio de Janeiro, Brazil
  5. Eric Ka Wai Hui- Vice President & Cofounder-ArmaGen, USA
  6. Marika Kamberi, Abbott Vascular, USA
  7. Gregory K Bell - Charles River Associates
  8. Yite Robert Chou, Merck & Co Inc., USA
  9. Eleonora Babayants  - President Galaxy Consulting ,USA

We extend our heartiest thanks to all the Organizing Committee Members for their kind support rendered towards the success of Pharmaceutical Analysis 2018. At the same time we take the opportunity to thank all the speakers, delegates and participants for providing their valuable contribution and time for Pharmaceutical Analysis 2018.

Pharmaceutical Analysis 2018 Organizing Committee would like to thank the Chairs and Co-Chairs of the conference, Yite Robert Chou, Kooros Motamed-Larijani, Mandla S Makhanya, who contributed a lot for the smooth functioning of this event.

 

To share your views and research, please click here to register for the Conference.

To Collaborate Scientific Professionals around the World

Conference Date June 27-28, 2018
Sponsors & Exhibitors Click here for Sponsorship Opportunities
Speaker Opportunity Closed Day 1 Day 2
Poster Opportunity Closed Click Here to View

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