GMPs for OTC and Cosmetic Products - US and Global Requirements 2016 is a webinar that covers topics such as:
- FDA Guidance Documents for OTC`s and Cosmetics
- Can OTC medicines be marketed without pre-approval from FDA?
- FDA`s review of OTC drugs is primarily handled by CDER`s Office of Drug Evaluation IV
- OTC Drug Products for existing Monographs
- CGMP regulations for OTC products contain minimum requirements for the methods, facilities, and controls used in manufacturing, processing, and packing of a drug product
- FDA ensures the quality of drug products by carefully monitoring drug manufacturers` compliance with its Current Good Manufacturing Practice (CGMP) regulations
- Good manufacturing practice (GMP) is an important factor in helping to assure that your cosmetic and OTC products are neither adulterated nor misbranded
- What are the requirements for manufacturing OTC drug products and cosmetics?
GMPs for OTC and Cosmetic Products - US and Global Requirements 2016 is intended for attendees from personal care, cosmetic, chemical application and pharmaceutical industries involved in:
- Technology, Formulation and Product Development
- Research & Development
- Regulatory Affairs
- Marketing & Technical Sales
- QA / QC
- Manufacturing
