Pharmacovigilance & Clinical Trials

Pharmacovigilance is defined as ,it deals with the science and the activities related for the collection, detection, assessment, monitoring, and prevention of the adverse effects of a drug or any other drug-related problem. Clinical trials are also known as research studies that explore whether a medical strategy, treatment, or device is safe and effective for humans. And these studies may also show which medical approaches are useful for the certain illnesses or groups of the people. Clinical trials will produce the best data available for health care decision making.

  • Clinical or Contract Research
  • Bioavailability of Drugs
  • Pre-formulation &Formulation aspects
  • Research Advancements in Drug Formulation
  • ADME Compliances
  • Continental Pharmacovigilance
  • Pharmacovigilance and Risk Management
  • Pharmacoepidemiology

Related Conference of Pharmacovigilance & Clinical Trials

January 29-30, 2026

19th World Drug Delivery Summit

Paris, France
February 10-11, 2026

40th World Congress on Pharmacology and Therapeutics

Barcelona, Spain
February 23-24, 2026

3rd World Congress on Biologics and Biosimilars

London, UK
March 23-24, 2026

36th Annual European Pharma Congress

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March 24-25, 2026

11th International Conference on Future Pharma and Innovations

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April 16-17, 2026

19th European Biosimilars Congress

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9th European Biopharma Congress

Paris, Aland Islands
May 28-29, 2026

3rd International Conference on Pharmacognosy

Madrid, Spain
July 27-28, 2026

39th World Congress on Pharmacology

Rome, Italy
September 24-25, 2026

6th World Congress on Rare Diseases & Orphan Drugs

Paris, France

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