2025 ISPE June Online Live Training
Deep Dive into Pharma Training Courses
Gain solutions to your company's immediate goals to lower production costs, improve process efficiency, increase production quality, and meet regulatory requirements.
- Real World Practice: Courses present exercises that use current problems and situations common to the industry.
- Experienced Instructors: Subject matter experts and top leaders in the pharmaceutical industry who have years of experience in their field of study.
- Global Training to Fit Your Needs: With eLearning
In-Person Training Events Online Live Training Events
In-Person Training Events
ISPE Hands-On Commissioning & Qualification (C&Q), Process Validation, and ATMP Training
16 - 18 June 2025
The course will cover qualification and process validation, from EU and US perspectives, considering both small and large molecule aspects, plus it will include a half day to consider qualification and process validation for ATMPs.
Instructor
Online Live Training Events
Pharma Facilities Project Management
3 - 6 June 2025
This course is structured around a typical facility project lifecycle of Project Initiation, Delivery Planning, Design Planning and Delivery, Procurement, Construction, Commissioning and Qualification and Project Close-Out & Review and uses case study examples throughout to illustrate key points.
Instructor
GAMP® 5 GxP Process Control
3 - 6 June 2024
The course covers recommended good practice based on a lifecycle approach for the development and management of process control systems and shows how the principles and concepts of GAMP 5 may be practically applied to process control systems. It looks at the data created by the process control system through the data lifecycle to understand how to protect against threats to data integrity. The course covers both regulated company and supplier quality management systems and the full system life cycle from concept to retirement.
Instructors
GMP Fundamentals for the Pharmaceutical Industry
9 - 12 June 2025
This course is designed to help participants understand the GMPs as they relate to the pharmaceutical industry. Participants will gather information about both European regulators and the FDA, how the various agencies enforce GMP requirements, and what to expect during a routine GMP inspection.
Instructor
Overview Biopharmaceutical Manufacturing Processes
16 - 19 June 2025
Explore commonly used manufacturing process operations including cell culture and fermentation; harvest and recovery; viral removal and inactivation; purification processes such as tangential flow filtration, centrifugation, size exclusion, and adsorptive chromatography.
Instructor
GAMP® Data Integrity 21 CFR Part 11 Training Course
24 - 26 June 2025
This course will cover data integrity, electronic records and signatures, and the compliant operation of GxP Computerized Systems to provide the tools and techniques to implement proper controls for data to ensure the integrity and validity of the information throughout the data lifecycle.
Instructor
