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Cloud Software Applications for 21 CFR Part 11

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Website | Edit Freely

Category Data Integrity, Cloud Software Applications, cloud computing software, cloud based software, saas application 2018, Compliance Online Programs, Compliance Solutions

Deadline: August 12, 2018 | Date: August 14, 2018

Venue/Country: Online, U.S.A

Updated: 2018-06-07 14:32:21 (GMT+9)

Call For Papers - CFP


This webinar demystifies Part 11, and get you on the right track

for using electronic records and signatures to greatly increase


Areas Covered in the Session:

Which data and systems are subject to Part 11

What Part 11 means to you, not just what it says in the regulation

Avoid 483 and Warning Letters

Explore the three primary areas of Part 11 compliance: SOPs,

software product features, and validation documentation

Ensure data integrity, security, and protect intellectual property

Who Will Benefit:




Laboratory Staff


GMP, GCP, GLP Professionals

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


Event Fee: One Dial-in One Attendee Price: US $290.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407


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.