Industrial & Regulatory pharmacy

Industrial Pharmacy includes in all areas such as manufacturing of new drug product,  and also development, marketing and distribution of drug products including quality assurance of these activities. This broad research area relates to different functions in pharmaceutical industry and having contact areas with engineering and economics. In pharmacy drug regulatory affairs refers to all aspects within the pharmaceutical development process of medicinal products and how they are subject to various degrees of regulation. The pharmaceutical law frame, guidelines covering Quality, Safety and Efficacy as well as Health Authorities' attitudes and requirements etc. have a great influence on the drug development process and the success of it. 

  • Supply chain management
  • Waste management
  • Product management
  • Post- marketing surveillance
  • Good manufacturing practices
  • Pharmaceutical companies and regulatory guidelines
  • Quality assurance in regulatory affairs
  • Regulatory affairs for clinical trails
  • Regulatory requirements of pharmaceutical products
  • Regulatory services and market analysis
  • US FDA guidelines

Related Conference of Industrial & Regulatory pharmacy

January 29-30, 2026

19th World Drug Delivery Summit

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3rd World Congress on Biologics and Biosimilars

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36th Annual European Pharma Congress

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19th European Biosimilars Congress

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39th World Congress on Pharmacology

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