How do the FDA CFR 21 Part 11 requirements relate to the VL-series system?
The CFR 21 Part 11 regulations apply to any electronic records that are used as a part of GMP documentation, including the ones produced by the VL-series data logging system. The following table summarizes the key requirements of the CFR 21 Part 11 regulations and how the VL-series system addresses those requirements. (For a complete summary, request the “White Paper on Veriteq 21 CFR Part 11 Compliance”.
