Ostrove Associates, Inc. (OAI) was founded in 1999 by Dr. Steven Ostrove in order to provide the Pharmaceutical and Bio-Pharmaceutical industries with expert guidance in CGMP compliance at reasonable cost. Our expertise rests on hands-on knowledge of the equipment and processes used throughout the industry. We know the regulations; we take a practical approach to their implementation and we do it at a reasonable cost.
Dr. Ostrove has over 30 years of experience in the Bio-Pharm industry including R&D, scale up, technical service and department management.A certified teacher, noted author and lecturer, Dr. Ostrove has been an invited speaker and trainer around the world on GMP and compliance issues and has served on an FDA Advisory Panel.
He has been an invited speaker and trainer around the world on GMP training and compliance issues. He has extensive experience in project management for compliance projects of all sizes. He built two departments, each to multi-million dollar revenue status, in fewer than 3 years. His project experience ranges from small GMP audits to qualifying multi-million dollar facilities.
Dr. Ostrove holds a BS degree from the State University of New York at Albany in Biology/Chemistry, an MS degree in Biology (cell culture) from Adelphi University and a Ph.D. degree in Biochemistry from Rutgers, the State University of New Jersey.
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