2019 - 21 CFR part 11 Compliance - electronic records & electronic signatures
Topics/Call fo Papers
Overview
This Webinar will explain what 21 CFR Part 11 is, 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 will be explained. 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
Why should you attend this webinar?
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 this means.
Areas Covered in the Session:
Company certification
Records covered
Audit trails
Open /closed system access rules
Electronic signatures
Training requirements
Who can Benefit:
Engineering personnel
Regulatory personnel
IT
Management
Speaker Profile:
Edwin Waldbusser is Keynote Speaker at ComplianceKey. He is retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices. QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/ control and manufacturing.
Register: https://www.compliancekey.us/webinarDetails?indust...
Contact Info:
Compliance Key
Email: support-AT-compliancekey.us
Visit: https://www.compliancekey.us/upcoming-webinars
Phone: 717-208-8666
This Webinar will explain what 21 CFR Part 11 is, 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 will be explained. 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
Why should you attend this webinar?
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 this means.
Areas Covered in the Session:
Company certification
Records covered
Audit trails
Open /closed system access rules
Electronic signatures
Training requirements
Who can Benefit:
Engineering personnel
Regulatory personnel
IT
Management
Speaker Profile:
Edwin Waldbusser is Keynote Speaker at ComplianceKey. He is retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices. QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/ control and manufacturing.
Register: https://www.compliancekey.us/webinarDetails?indust...
Contact Info:
Compliance Key
Email: support-AT-compliancekey.us
Visit: https://www.compliancekey.us/upcoming-webinars
Phone: 717-208-8666
Other CFPs
- 2019 International Conference on E-Business and E-Commerce Engineering (EBEE 2019)--EI Compendex and Scopus
- The UK Careers Fair in Derby - 14th June
- 32nd Materials Science and Engineering Conference: Advancement & Innovations
- International Conference of Artificial Intelligence and Fuzzy Logic (ICAIL 2019)
- 2019 International Artificial Intelligence Technology Conference (AITC 2019) will be held during November,27-29, 2019 in Hangzhou, China
Last modified: 2019-04-25 18:20:45