Over two decades, QPharma has played a leadership role in guiding the implementation of regulatory compliance best practices throughout the life sciences industry. Our subject matter experts don’t simply interpret the regulations; they actively contribute to their development and continuous refinement. QPharma’s trainers have conducted compliance seminars, lectures, and workshops throughout the nation and around the world.
Whether our clients need a one-day, Internet-based executive session or a comprehensive, on-site technical series spanning several days or weeks, QPharma has the knowledge and resources to deliver a top-quality training solution. We also offer online training and certification solutions for life sciences sales forces. If you don’t see a topic listed here, simply ask — we’re at your service to develop a custom educational program to meet any client need.
A Comprehensive Variety of Topics
- Project Management
- Validation Planning
- Process Validation
- 21 CFR Part 11
- PDMA Compliance
- FDA, DEA, and other Regulatory Authorities
- Sunshine Act/Aggregate Spend
- Quality System Regulations
- Current Good Manufacturing Practices
- Custom Topics on Request
To engage QPharma to develop an innovative training solution for your team, please contact us.