 The Process Validation certification program is ideal for anyone in the Pharmaceutical, Medical Device, Biotech, Biopharmaceutical and Skin/Cosmetic industries who is tasked with process validation. Personnel involved in validation activities from product development through post-approval production concerns will find comprehensive insight on what regulators are looking for. This program requires completion of three of four core courses. Pharmaceutical personnel should select the Process Validation for Drugs and Biologics course and participants from Medical Device manufacturers should choose Process Validation for Medical Devices.
To complete your Process Validation certification, you must also complete one elective course from the list below. Simply choose a course that is of the most interest to you or most relevant to your current position:
Core Courses (Choose Three):
- Validation of Computer Systems
- Process Validation for Drugs and Biologics
- Process Validation for Medical Devices
- Writing Effective Standard Operating Procedures and Other Process Documents
- Best Practices for an Effective Cleaning Validation Program
Elective Courses (Choose One):
- Overview Of FDA Regulatory Compliance For Medical Devices
- Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
- Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
- Practical Methods for Project Management
- Reporting Failure Investigations and Process Deviations
- Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
- cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
- Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Please contact CfPIE at +1-610-688-1708 or via email at info@cfpie.com for more information, or to register for any course.
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