Process Validation for cGMP Dietary Supplements
We know you want to rest assured that every critical piece of equipment and every step in your cGMP process is going to deliver a high quality product every time. Just testing at the end of manufacturing is not enough. You want to make sure you are building quality into each step of the process so the end-product testing is only a confirmation of what you already know – you are making the best product possible. We along with our partners at PharmaDirections can help you validate your equipment and your processes.Our Process Validation Services include:
- Risk Assessment
- Master Validation Plan
- Validation Protocol Design
- Design of Experiments and Statistical Analysis
- Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
GMP Compliance Series LinksPart 1: Improving Documentation of GMP Procedures
Part 2: Better Compliance through Master Manufacturing Records
Part 3: Improving Batch Production Records
Part 4: Specifications That Improve Compliance
Part 5: Improving Quality through In-Process Control
Part 6: Documenting Deviations for Improved Compliance
Part 7: Supplier and Vendor Qualification
InstantGMP™ MES: The only cloud based Manufacturing Execution System designed to make it easy to manufacture products regulated by the FDA.