ConferenceSeries Ltd organizing splendorous Pharmaceutical conferences welcomes you to attend the 5^th Global Pharmacovigilance Summit to be held during April 28-29, 2016 in Dubai,UAE focuses on the advancements in pharmacovigilance and risk management.

Track-1: Drug Safety:

Drug Safety or Pharmacovigilance (PV or PhV), is the  study of Pharmacology  related to the data collection, assessment, detection,  monitoring, and prevention of adverse effects with drug products. In this Track we will discuss about  Drug safety awith its importance in various fields as Training, softwares etc. & other topics which are  discussed in Pharmacovigilance Conferences

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques ,March 17-18, 2016, London, UK; Asia Pacific Drug Formulation & Bioavailability Congress, Beijing, China, June 06-08, 2016; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA ; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA;2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; SCT 37^th Annual Meeting (2016); Conference on Pharmacology and Toxicology Research; Pharmacovigilance Conferences and Risk Management Strategies 2016

Track-2: Adverse Drug Reactions:

Adverse drug reaction (ADR) can be defined as a damage caused by taking a medication. Most of the adverse drug reactions represent an enhancement  of the drug's therapeutic effects. There are various types of Adverse Drug Reactions and its effect on the body. Proper assessment and reporting of adverse drug reactions is important for drug safety systems. In this track we will focus on  Expected and un-expected drug reactions and its reporting. Even drug product manufacturers, professionals, and consumers can report Post marketing reports on adverse effects & other topics which are  discussed in Pharmacovigilance Conferences

Related Conferences:

2^nd International Conference on Clinical Trials , August 22-24, 2016, Philadelphia, USA; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; Asia Pacific Drug Formulation and Bioavailability Congress ,  Beijing, China, June 06-08, 2016; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference; Pharmacovigilance conferences and Clinical Trials; Conference on Pharmacovigilance and Drug Safety

Track 3: Pharmacovigilance Significance&Scope:

The focus in the track named Pharmacovigilance and its Significance and Scope will be on importance of pharmacovigilance. It will help to analyze its  potential as a major discipline within medical science, and to find out its influence on patient health and public welfare. This will help to better understand what is pharmacovigilance. In  Pharmacovigilance Practice we will come to know about Pharmacovigilance legislation, the rules and laws to follow. Pharma Industries have a major role in the improvement of Pharmacovigilance system to maintain the safety data.  Pharmacovigilance Conferences also deals with  Ecopharmacovigilance (EPV), pharmacoenvironmentology and pharmacovigilance in herbal medicines.

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK ; Asia Pacific Drug Formulation and  Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016,Dallas,USA; 6^thInternational Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR,  September 12-14, 2016, San Atonio, USA ; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference ; Conference on Pharmacovigilance and Drug Safety ; Pharmacovigilance Conferences and Clinical Trials

Track 4: Continental Pharmacovigilance:

Continental Pharmacovigilance provides a scope  to ensure compliance with local and international requirements, to operate more efficiently across various regions and health authorities.

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK ; Asia Pacific Drug Formulation and  Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016,Dallas,USA; 6^thInternational Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR,  September 12-14, 2016, San Atonio, USA ; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference ; Conference on Pharmacovigilance and Drug Safety ; Conference on Pharmacovigilance and Clinical Trials

Track 5: Good Pharmacovigilance Practice:

Pharmacovigilance and Pharmacoepidemiology role in the  risk management mainly focusses on  to overcome  insufficient evidence of safety from clinical trials. Good Pharmacovigilance  Practice avoids major problems in risk management which are discussed in Pharmacovigilance Conferences. It is of high importance to focus  on Signal investigation via observational studies and Interpreting safety signals. Concentrating on dosages forms in random clinical trials is very important. The Pharmacovigilance clinical trials service providing companies should have the Pharmacovigilance certification .

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK ; Asia Pacific Drug Formulation and  Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016,Dallas,USA; 6^thInternational Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR,  September 12-14, 2016, San Atonio, USA ; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference ; Conference on Pharmacovigilance and Drug Safety ; Conference on Pharmacovigilance and Clinical Trials

Track-6: Pharmacovigilance and Risk Management:

Pharmacovigilance and Risk Management play a major role in Drug Industry. The new turn in Drug Industry is to use Information technology in pharmacovigilance companies. Drug industry needs to promote companies in pharmacovigilance Practice and the Review of Softwares used in Pharmacovigilance and Clinical Trials. Monitoring of  unlicensed, off labels and orphan drugs is major task in risk management. In this conferences so many experts from different Pharmacovigilance CRO's ,pharmacovigilance service providers are participating to shares their knowledge and discuss about the new updates. In 2016  there is a Pharmacovigilance Conference , which is going to be held in Dubai, on April 28-29.

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques ,March 17-18, 2016, London, UK; Asia Pacific Drug Formulation & Bioavailability Congress, Beijing, China, June 06-08, 2016; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA ; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA;2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; SCT 37^th Annual Meeting (2016); Conference on Pharmacology and Toxicology Research; Pharmacovigilance Conferences and Risk Management Strategies 2016

Track-7: Pharmacokinetics and Pharmacodynamics:

Drugs at various steps undergo, Pharmacokinetics and Pharmacodynamics and toxicity testing through animal testing. These tests allow researchers to allometrically find out a safe starting dose of the drug for clinical trials in humans. This track will be  revolving around  Advances in Pharmacodynamic Interactions, Drug and substance abuse, Drug-drug interactions. Also discussion will be about the Pharmacy Practices to maintain the Pharmacokinetics and Pharmacodynamics, its Challenges and its guidelines. There are several challenges in compounding and dispensing practice in Pharmacokinetics and Pharmacodynamics which are also covered in Pharmacovigilance Conferences

Related Conferences:

Asia Pacific Drug Formulation and Bioavailability Congress , June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA;  2^nd International Conference on Clinical Trials , August 22-24, 2016, Philadelphia, USA; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ;6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference; Pharmacovigilance Conferences and Drug Safety; Conference on Pharmacovigilance and Clinical Trials

Track 8: Pre-Clinical and Clinical Trials:

The main goals of Pre-Clinical and Clinical Trials are to determine the safe dose and start to assess product's safety profile. In Designing of trials there are pre-clinical studies and different phases of clinical trials. In this trails they estimate the Bioassay and its types. The Data collection and quality control is the major part in Pre-Clinical and Clinical Trials. For some specific drugs there are some Alternative trials designs and models are used. Pre-Clinical and Clinical Trials are conducted as Multi center trials and monitoring basis. Each Pre-Clinical and Clinical Trials study of a drug, biological product, or medical device regulated by the FDA must be reviewed, approved, and monitored by the Regulatory authorities and ethics committee. There are several types of clinical trials like Clinical trials on drugs used in respiratory disorders. Advanced Information technology in clinical trials improves the quality of Pre-Clinical and Clinical Trials which are a part of Pharmacovigilance Conferences

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8^th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems , June 06-08, 2016, Beijing, China; Asia Pacific Drug Formulation & Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA; Anatomy and Physiology-2016, August 11-13, 2016, Birmingham, UK ; 2^nd International Conference and Expo on Drug Discovery & Designing, October 24-26, 2016, Istanbul, Turkey; Outsourcing in Clinical Trials Europe 2016; 5^th Annual Clinical Development and Trials Asia Congress; SCT 37^th Annual Meeting (2016); Outsourcing in Clinical Trials East Coast 2016; Pharmacovigilance Conferences and Clinical Trials

Track-9: Clinical Trials on Various Disorders:

Clinical Trials on Drugs used in Various Disorders, Pharmacotherapy and Pharmacotherapeutics Emerging technology in clinical trials track mainly deals on the clinical trials in long chronic diseases and several disorders. In This track we will be discussing about the Recent clinical trials on AIDS, Clinical trials on benign and malignant tumours, Clinical trials on cardiovascular diseases, Clinical trials on diabetes, Clinical trials of monoclonal and polyclonal antibodies, Clinical trials on drugs used in psychological disorders The current research mainly focuses on Applications of biomarkers in clinical trials. These are a part of Pharmacovigilance Conferences

Related Conferences:

8^th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems , June 06-08, 2016, Beijing, China; Asia Pacific Drug Formulation & Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA; Anatomy and Physiology-2016, August 11-13, 2016, Birmingham, UK ; 2^nd International Conference and Expo on Drug Discovery & Designing, October 24-26, 2016, Istanbul, Turkey; Outsourcing in Clinical Trials Europe 2016; 5^th Annual Clinical Development and Trials Asia Congress; SCT 37^th Annual Meeting (2016); Outsourcing in Clinical Trials East Coast 2016; Pharmacovigilance Conferences and Clinical Trials

Track-10: Clinical Research and Statistics:

In Clinical Research Statistics plays major role. Depends upon the Statistics the clinical trials go for regulatory submissions. There are several guidelines mainly ICH guidelines for clinical research and its statistics follow for the clinical research. Stastical analysis of past pharmacovigilance conferences and adverse drug reactions reports also consider for the regulatory submission.

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8^th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems, March 07-09, 2016, Madrid, Spain; International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK; International Conference and Exhibition on Medical Writing and Healthcare Communications, April 28-29, 2016, Dubai, UAE; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA; International Conference on Precision Medicine, November 03-05, 2016, Baltimore, USA; Conference on Pharmacodynamics, Biomarkers and Personalised Therapy; Conference on Drug Formulation, Bioavailability and Pharmacy; Conference on Drug Formulation, Bioavailability and Pharmacological Sciences; Conference on Developing Countries and Pharmacological Sciences; Conference on Pharmacology and Toxicology Research

Track-11: Case Report in Clinical Trials:

Case Report in Clinical Trials plays major role in clinical research. In this track focus will be  about the several case reports like Cancer case reports, Cardiovascular trials case report, Case studies on sexually transmitted diseases, Case studies on type 1 and type 2 diabetes, Case reports on drugs used in pregnancy and lactation.

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8^th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems, March 07-09, 2016, Madrid, Spain; International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK; International Conference and Exhibition on Medical Writing and Healthcare Communications, April 28-29, 2016, Dubai, UAE; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA; International Conference on Precision Medicine, November 03-05, 2016, Baltimore, USA; Conference on Pharmacodynamics, Biomarkers and Personalised Therapy; Conference on Drug Formulation, Bioavailability and Pharmacy; Conference on Drug Formulation, Bioavailability and Pharmacological Sciences; Conference on Developing Countries and Pharmacological Sciences; Conference on Pharmacology and Toxicology Research

Track-12: Biopharmaceutics:

In Clinical Pharmacology and Bio pharmaceutics track discussion will be about the Rational drug management of cancer, diabetes and cardiovascular disorders, and Management of psychiatric disorders and autoimmune disorders. Along with clinical trials Bioavailability and bioequivalence studies also plays major role in clinical research.

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8^th International Conference and Exhibition on Pharmaceutics and Novel Drug Delivery Systems, March 07-09, 2016, Madrid, Spain; International Conference and Exhibition on Advances in HPLC and Chromatography Techniques, March 17-18, 2016, London, UK; Asia Pacific Drug Formulation and  Bioavailability Congress, June 06-08, 2016, Beijing, China; 7^th World Congress on Bioavailability and  Bioequivalence: BA/BE Studies Summit, August 29-31, 2016, Atlanta, USA; 5th Biologics and Biosimilars Conference, September 12-14, 2016, San Antonio, USA; Conference on Biomedical and Pharmaceutical Sciences; Conference on Drug Formulation, Bioavailability and Pharmacological Sciences; Conference on Biopharmaceutics and Drug Delivery Systems; Conference on Biopharmaceutics and Pharmacodynamics; Conference on Biopharmaceutical and Life Sciences

Track-13: PV Data Base Management:

There is advantage in centralising all safety data, clinical data, analysis and reporting with one provider. Pharmacovigilance Software tool provides comprehensive analysis of adverse events arising from the use of pharmaceutical products (Medicinal Product, Medical Device, Vaccines, Non-Drug Therapy and Veterinary Medicinal Product). The drug safety database allows the risk- benefit analysis of medicinal products taking into account new and emerging information, in the context of cumulative information. Pharmacovigilance since beginning has been a compliance driven activity, wherein your regulatory compliance determines company’s risk assessment scores. A drug safety database offers scheduling of alerts for expedited cases, follow-up cases and PSUR/PADER reports submission to meet regulatory timeline compliance. PV database is also covered in Pharmacovigilance Conferences

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International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK ; Asia Pacific Drug Formulation and  Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016,Dallas,USA; 6^thInternational Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR,  September 12-14, 2016, San Atonio, USA ; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference ; Conference on Pharmacovigilance and Drug Safety ; Pharmacovigilance Conferences and Clinical Trials

Track-14: PV Consulting’s and Business opportunity:

Due to the changing resources necessary to fulfil the regulatory requirements, some companies also choose to outsource or out task regulatory affairs to external service providers. Regulatory Affairs department is constantly evolving and growing and is the one which is least impacted during the Acquisition and Merger, and also during recession. The stringent regulations on safety monitoring and their periodical revision have led to increased safety data collection, analysis and regulatory surveillance, and increased costs. Thus, Pharmacovigilance has become a critical phase in clinical development programs.

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK ; Asia Pacific Drug Formulation and  Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016,Dallas,USA; 6^thInternational Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR,  September 12-14, 2016, San Atonio, USA ; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; Pharmacovigilance and Risk Management Strategies 2016; EGA Pharmacovigilance Conference ; Conference on Pharmacovigilance and Drug Safety ; Pharmacovigilance Conferences and Clinical Trials

Track-15: Regulatory affairs:

Regulatory affairs for clinical trials is the major part in the clinical trials approaches. Every clinical trial must be conduct according to the Regulatory affairs guidelines. There are several Regulatory affairs depending upon the countries. Regulatory Affairs departments are growing within companies. Global harmonization in standards has led to consistent approach in regulatory submissions and hence its review.

Related Conferences:

International Conference and Exhibition on Advances in HPLC and Chromatography Techniques , March 17-18, 2016, London, UK ; Asia Pacific Drug Formulation & Bioavailability Congress, June 06-08, 2016, Beijing, China; 2^ndInternational Conference on Therapeutic Drug Monitoring and Toxicogenomics , June 09-10, 2016, Dallas, USA; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA; 2^nd International Conference and Expo on Drug Discovery and Designing, October 24-26, 2016, Istanbul, Turkey ; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; SCT 37^th Annual Meeting (2016); Conference on Pharmacology and Toxicology Research; Pharmacovigilance and Risk Management Strategies 2016

Track-16: Growth strategies in Pharma:

Strategies for Growth in Pharma Environment track mainly focused in Strategic development towards FDA approval and Post market product surveillances. The updates and advances in pharmacovigilance regulation system will be discussed in Advances in changing pharmacovigilance regulation system track. These strategies are covered in the Pharmacovigilance Conferences

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8^th International Conference and Exhibition on Pharmaceutics and  Novel Drug Delivery Systems  , March 07-09, 2016, Madrid, Spain; International Conferences and Expo on Industrial Pharmacy, April 28-29, 2016, Dubai, UAE;  6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, , September 12-14, 2016, San Atonio, USA; Conference on Pharmacy and Pharmaceutical Sciences; Conference on Pharmaceutical Analysis; Conference on Pharmacy and Pharmacological Sciences; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; SCT 37^th Annual Meeting (2016)

Track-17: Pharmacy Practices and its Challenges:

In Pharmacy Practices and its Challenges track mainly focused on Pharmacy practice and its guidelines and Challenges in compounding and dispensing practice. Dosage regimen, drug toxicity and drug safety measures place important position in clinical research.

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8^th International Conference and Exhibition on Pharmaceutics and  Novel Drug Delivery Systems  , March 07-09, 2016, Madrid, Spain; International Conferences and Expo on Industrial Pharmacy, April 28-29, 2016, Dubai, UAE; World Drug Delivery Summit, June 30-July 02, 2016, New Orleans, USA; 6^th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR, September 12-14, 2016, San Atonio, USA; International Conference on Pharma Marketing, November 17-19, 2016, Alicante, Spain; Conference on Pharmacy and Pharmaceutical Sciences; Conference on Pharmaceutical Analysis; Conference on Pharmacy and Pharmacological Sciences; 6^th Annual Pharmacovigilance and Risk Management Strategies Forum; SCT 37^th Annual Meeting (2016)