VTS Consultants

Training Sessions

The following training session topics have been some of the ones given to various companies and through professional organizations. Training sessions are custom tailored to the client’s needs, knowledge level of the audience and level of detail requested. VTS Consultants have given training sessions to audiences ranging from 7 to over 300 people around the world.
•    Equipment and Computer Change Control
•    General Qualification Requirements of IQ/OQ and PQ Protocols
•    Computer System Validation Requirements
•    High Purity Water System Validation Requirements
•    Validation Requirements for Sterile Products
•    How to Prepare for FDA Audits of Sterile Manufacturing Facilities
•    Aseptic Manufacturing Processes
•    Quality Assurance Practices and Expectations
•    Process Validation Requirements
•    Good Documentation Practices
•    Vendor Quality Agreements
•    Quality System Requirements for Preventative maintenance, calibration and cleaning programs.
VTS has provided training in association  with the PDA, ISPE, The Institute for International Research (IIR), FDANews, Pharmaceutical Training International (PTI) and IPA of Canada (International Pharmaceuticals Academy) to name a few.  We also provide customized training for “In-House” cGMP presentations to save our clients money and to have the training given to as many employees as possible.
For a current list of scheduled training sessions, please visit our “Training Events” page

FDA Audit Practices: the 10 Most Commonly Cited Drug GMP Deficiencies of 2012-2013