Successful system validation for GLP, GCP, cGMP and 21 CFR11
Validating analytical hardware, software and methods–plus ensuring data security, integrity and traceability can be time-consuming and costly.Our hardware and software offer more built-in compliance features than any other systems on the market. You can validate your systems, methods and data in the shortest possible time and at the lowest cost.
To make regulatory compliance even easier, Agilent Technologies support services offer fast, affordable compliance solutions.
Five steps guide you to fast, cost-effective and successful validation:
1) Design qualification (DQ)
2) Installation qualification (IQ) and operational qualification/performance verification (OQ/PV)
3) Method validation
4) Performance qualification (PQ)
5) Electronic records protection for compliance with 21 CFR Part 11
- E-seminar series provides basic and update information on validation and compliance in laboratories.
- Comprehensive primer describing the basics of GLP and cGMP and their impact on analytical work.
- Brochure describing validation and compliance solutions for analytical laboratories.
- Compliance Services offered by Agilent Technologies.
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