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.