Instructor:
Michelle Sceppa
Product ID: 701188
It is a Regulatory Requirement to establish a program for the preventive maintenance and calibration requirements for equipment and instrumentation used for characterization, testing and/or release of pharmaceutical & biotechnology products.
Areas Covered in the seminar:
Who will benefit:
This webinar will provide instruction on how to establish and maintain a Maintainance & Calibration program for pharmaceutical instrumentaition & equipment
Instructor Profile:
Michelle Sceppa, is the Principal at MSceppa Consulting, an establish Consulting firm and is in its 12thth year in the Industry that specializes in quality systems for Pharmaceutical and Biotechnology interests. MSceppa Consulting has implemented and managed Preclinical, Clinical, and Manufacturing Quality Assurance Programs for numerous clients. As the lead auditor, MSceppa Consulting has conducted and managed more than 400 internal and external vendor audits for Drug and Biologic firms in the US and Europe. MSceppa Consulting is knowledgeable in the details of compliance with all U.S. Federal Regulations-Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP) for Drugs, Biologics and Medical Devices.
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