Course Overview
This comprehensive program covers three critical modules: Good Laboratory Practices (GLP), Good Distribution Practices (GDP), and Good Documentation Practices (GDP), designed to enhance operational excellence in the pharmaceutical industry. Participants will gain practical insights into regulatory compliance, risk management, and effective documentation through real-world case studies, interactive simulations, and actionable exercises. The course equips professionals with the skills to tackle challenges in laboratory operations, distribution systems, and technical writing, emphasizing situational awareness and industry-specific best practices. By the end, participants will have actionable takeaways to implement in their daily workflows.
Features
- To equip participants with practical knowledge and situational awareness required for regulatory compliant lab operations, with insights from real-life scenarios and industry challenges.
- To provide actionable insights into managing distribution risks, ensuring compliance with GDP, and improving supply chain resilience through real-world examples.
- To empower participants with practical skills in documentation and technical writing, focusing on real-world applications, compliance challenges, and effective communication.
Target audiences
- Quality Assurance
- R&D
- Regulatory & Compliance Teams
Instructor
