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. The global biologics market totaled $200.6 billion in 2013 and is expected to grow to nearly $234 billion in 2014. The total market is expected to grow to $386.7 billion by the end of 2019 at compound annual growth rate (CAGR) of 10.6%.

  • Regulatory Guidelines
  • USFDA
  • EU
  • MHRA
  • Medical writing Pharmacovigilance

Related Conference of Regulatory affairs

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International Pharmacy Conference

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5th Annual European Pharma Congress

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Holiday Inn Birmingham City Centre, Birmingham,UK
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7th Annual Global Pharma Summit

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Drug Formulation & Bioavailability Congress

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4th Global Experts Meeting on Neuropharmacology

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International Conference on Pain Research & Management

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8th Annual Pharma Middle East Congress

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World Pharma Congress

Las Vegas, Nevada, USA
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8th Global Pharmacovigilance Summit

Melbourne, Australia
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International Conference on Medical Devices

Orlando, USA
May 25-26, 2017

World Congress on Biotherapeutics

Mexico, USA
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World Congress on Controlled/ Sustained Release Formulations

Amsterdam, Netherlands
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8th Asian Biosimilars Congress

Japan
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Annual Pharmaceutical Analysis Conference

Vienna, Austria
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Regulatory affairs Conference Speakers

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