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OVERVIEW
FDA regulated companies want to transition to electronic records for economy and efficiency. FDA, because of its concern for patient safety, wants to prevent electronic records from being compromised with possible resulting harm to the patient.
FDA has set up regulations that address both data security and patient safety. We will show how 21 CFR part 11 considers both.
The confusion over the original FDA regulation and its subsequent “selective enforcement” will be explained. FDA requirements for 21 CFR Part 11 validation will be explained. The requirements are composed of technical and procedural aspects.
Open, Closed and Hybrid (paper and electronic) systems will be explained.
WHY SHOULD YOU ATTEND
Companies want to transition to electronic records but are afraid of compromising their quality system and receiving 483’s at their next inspection. Part of this fear originates from confusion.
FDA originally published a rather severe 21 CFR Part 11. After industry complaints the FDA acknowledged that the regulation, as written, would result in nobody attempting to convert to electronic records. But, instead of rewriting the regulation, FDA said it would “selectively enforce” sections of the regulation.
This webinar will explain what all of this mean. An FDA 21 CFR part 11 compliance checklist and a Test protocol form will be given as handouts.
AREAS COVERED
Origin of the FDA regulation and changes in interpretation ; electronic records; CFR electronic signature; data security; open, closed and hybrid systems; validation methods; risk analysis.
LEARNING OBJECTIVES
This Webinar will explain what is FDA 21 CFR part 11 compliance, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security.
Procedures for controlling electronic signatures and electronic records as described in the FDA regulation will be explained.
WHO WILL BENEFIT
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