Regulatory Affairs, Drug Safety & Utilization Research

Regulatory Affairs is involved in all the stages of development of a new medicine and its post-marketing activities with medicinal products authorities. This department heart of pharmaceutical industry. Internally it is a cluster of drug development, drug manufacturing, drug marketing and clinical research. Outward it is an interface between the company and regulatory authorities. Regulatory affairs are independent for specific country and their guidelines. Drug safety and Utilization Research  promoting, dissemination, medicine, and utilization of medications in a general public, with uncommon action on the subsequent therapeutic, social and monetary outcomes. From that point then, various different terms have come into utilization and it is important to comprehend the interrelationships of the distinctive areas. The principal aim of drug utilization research is to facilitate the rational use of drugs in populations. For the individual patient, the rational use of a drug implies the prescription of a well documented drug at an optimal dose, together with the correct information, at an affordable price.

  • Medical Product Safety Surveillance
  • Pre-marketing & Drug utilization review
  • Cohort studies & Bias Studies
  • Pharmacoeconomics
  • Characterization of drugs and bio-therapeutics
  • Rapid methods to assess quality and stability of bio-therapeutics

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14th International Conference on Biopharma and Biotherapeutics

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20th Annual Pharma Middle East Congress

Istanbul, Turkey
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27th Global Experts Meeting on Neuropharmacology

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20th Annual Meet on Pharmaceutical Sciences

Bangkok, Thailand
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European Congress on Nanomedicine and Pharmaceutical Nanotechnology

Prague, Czech Republic
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Prague | Czech Republic
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13th European Biosimilars Congress 2020

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