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Compliance with 21 CFR Part 11 (Data Integrity)

View: 73

Website https://www.compliance4all.com/control/w_product/~product_id=502237LIVE?channel=ourglocal_Dec_2018_S | Edit Freely

Category Auditors, Managers and Directors, Software Vendors, Hosting Providers

Deadline: December 09, 2018 | Date: December 11, 2018

Venue/Country: Online, U.S.A

Updated: 2018-10-08 14:43:16 (GMT+9)

Call For Papers - CFP

Overview:

It explains how to write a Data Privacy Statement for compliance with EU

General Data Protection Regulation (GDPR).

Areas Covered in the Session:

What 21 CFR Part 11 means today

Purpose of Part 11

What does Part 11 mean?

SOPs

System features

Infrastructure qualification

Validation

Who Will Benefit:

GMP, GCP, GLP, Regulatory Professionals

QA/QC

IT

Auditors

Managers and Directors

Software Vendors, Hosting Providers

Speaker Profile:

David Nettleton, is an FDA Compliance Specialist for 21 CFR Part 11,

HIPAA, and Computer System Validation. His latest book is "Risk Based

Software Validation - Ten easy Steps" that relates to the development,

purchase, installation, operation and maintenance of computerized

systems used in regulated applications.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.