Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations (Updated to address recent Homeopathic Drug announcements by FDA & FTC)

Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations (Updated to address recent Homeopathic Drug announcements by FDA & FTC) covers topics such as:

  • Basic requirements for marketing homeopathic OTC drugs
  • Legal definitions of cosmetics, drugs and dietary supplements
  • Regulation differences in allopathic (conventional) drugs and homeopathic drugs
  • Formulation and label of cosmeceuticals products
  • Recent FDA Public Hearings aimed at changing the current FDA OTC Monograph System
  • Minimize the regulatory risk of a Warning Letter or other FDA action

Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations (Updated to address recent Homeopathic Drug announcements by FDA & FTC) brings together:

  • Product Managers
  • Senior Managers / Business Owners
  • Regulatory and Quality Professionals
  • Labeling and Artwork Designers
  • R&D Managers and Staff
  • Sales and Marketing Managers

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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