Training

Oral Solid Dosage Manufacturing Process Training Course (T10)

This training course examines current technology and provides scenario-based exercises for system troubleshooting and investigational events for process deviations, discusses quality management and GMP inspection preparation, and provides guidance on advanced asset lifecycle management strategy.
Explore the Programme (ED)

Explore the Programme


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Training

Managing Cross Contamination with Risk-MaPP Training Course (T41)

This course will focus on using the logic diagram, how cross contamination control fits into the Quality System, how health-based limits are developed, setting cleaning validation limits, risk assessments for cross contamination and formulation a Quality Risk Management Plan.
Training

Implementing Process Analytical Technology Training Course (T29)

This course is designed to help pharmaceutical manufacturing professionals chart a new course for innovation based on PAT. The course provides an overview to the tools and principles outlined in the FDA guidance, PAT - A Framework for Innovative Pharmaceutical Development, Manufacturing and Quality....
Training

Combination Products: Challenges and Expectations Training Course (T47)

Combination Products: Challenges and Expectations (T47) Overview With the increasing regulatory scrutiny on combination products, this new highly interactive course provides six (6) different aspects of a combination product which are: Combination Product GMPs Criticality of Design Input and how to....
Online Live Training

HVAC & Environmental Control for Life Science Facilities Training Course (T14)

This training course focuses on common issues and problems in the operation of a facility and maintaining readiness for cGMP inspection. Topics include control system alarm management, common system construction deficiencies, cGMP documentation, maintaining an "inspection ready" state, frequency of....
Training

ICH Q7A GMPs for Active Pharmaceutical Ingredients Training Course (T30)

This course covers areas in which compliance requirements differ most from traditional pharmaceuticals and biologics and will review common deficiencies and problem areas related to the ICH Harmonised Tripartite Guideline Good Manufacturing Practice Guide For Active Pharmaceutical Ingredients Q7 and....
Training

GMP Fundamentals for the Pharmaceutical Industry (G01)

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. They....
Training

GAMP® Data Integrity 21 CFR Part 11, 3-Day Training Course (T50)

This GAMP Data Integrity 21 CFR Part 11 Training 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.

CaSA 25th Annual Life Sciences Technology Conference

13 March 2018 - 13 March 2018
SAVE THE DATE (March 13, 2018): 25th Annual ISPE-CaSA Life Sciences and Technology Conference Raleigh Convention Center Tuesday, March 13, 2018
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