Dr. Ostrove has been involved in the Bio-Pharmaceutical business for over 35 years. He recently published a book titled “How to Validate a Pharmaceutical Process, 1st Edition” and is a recognized speaker at industry conferences.
Steve’s Bio Video | GMP Course Video
Good Manufacturing Practices (cGMP)
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
Process Validation for Drugs and Biologics
CfPIE Announces New Training Course on the Regulated Medical Marijuana Business
CfPIE Improves Website Experience for Life Science Training Attendees
CfPIE Announces New Regulatory Compliance Training Course for Compound Pharmacies
CfPIE Discusses Life Sciences Training Advancements at Regulatory Conferences
New CAPA Process Course for Medical Device Professionals
Partnership with the Society for Clinical Data Management
The Center for Professional Innovation and Education (CfPIE) provides technical training for Pharmaceutical, Biotech, Medical Device and Skin/Cosmetics professionals. CfPIE offers more than 350 class sessions annually across 80 course titles in multiple formats, such as classroom, on-site and certification programs.
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