Fundamentals of Pharmaceutical and Biologics Regulations Bundle (Hardcover)

This bundle comprises the pharmaceutical and biologics subsets from RAPS’ four Fundamentals of Regulatory Affairs books: US, EU, Canada and International. The subsets review requirements throughout the lifecycle of biopharma products, from R&D through postmarketing requirements in these regions. Bundled together, they make excellent resource to find answers to questions about pharmaceutical and biologics and products and to learn more about the industry. It also is an outstanding study toolfor the new RAC Drug exam.

Included in the bundle

• Fundamentals of US Pharmaceutical and Biologics Regulations
• Fundamentals of EU Pharmaceutical and Biologics Regulations
• Fundamentals of Canadian Pharmaceutical and Biologics Regulations
• Fundamentals of International Pharmaceutical and Biologics Regulations