Training

Deep Dive into Pharma Training Courses

Join us in person for hands-on training that delivers practical solutions to your company's critical challenges. Through interactive sessions and direct engagement with industry experts, you'll gain actionable strategies to optimize costs, improve process efficiency, enhance production quality, and ensure regulatory compliance. This face-to-face learning experience offers unique networking opportunities and real-time problem-solving with peers and instructors.

 

Key Benefits:

  • Real World Practice: Courses present hands-on exercises and interactive discussions using current problems and situations common to the industry.
  • Experienced Instructors: Learn directly from subject matter experts and top leaders in the pharmaceutical industry who have years of experience in their field of study.
  • Personalized Learning Experience: Benefit from face-to-face interaction, direct Q&A opportunities, and valuable networking with industry peers and experts.
  • Interactive Workshop Format: Engage in collaborative problem-solving and gain practical insights through in-person demonstrations and group exercises.

GAMP Basic Principles Training Courses

15 - 16 May 2025

 

This classroom course has been updated to include the new revised GAMP® 5 Second Edition. This fundamental course introduces participants to regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explores tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner.
 

GAMP 5 Guide 2nd Edition

Cleaning Validation

15 - 16 May 2025

As cleaning technology and detection methodology advance, so do the challenges associated with establishing, managing, and maintaining a scientifically sound cleaning validation program. With the FDA's risk-based regulatory initiatives focusing new attention on the risks of cross-contamination understanding lifecycle management techniques for an effective cleaning validation program is paramount. This training course covers the risk-based approach to cleaning development and verification; risk analysis; procedures and evaluation tools including FMEA / FMECA, master planning, risk control, PAT, periodic assessment and monitoring, risk review and communication.

Guide: Cleaning Validation Lifecycle - Applications, Methods, & Controls

Training Venue

Novotel London West

Novotel London West

One Shortlands, Hammersmith
London
W6 8DR 
United Kingdom
Hotel & Reservations:  (+44) 20 8741 1555