Technology Conference Listing
Featured: InterDrone, The International Drone Conference, Las Vegas, Sept 6-8, 2017
Featured: Women in STEM Conference and Award, San Francisco, Sept 10-12, 2017
Featured: PrecisionAg Vision Conference, Phoenix, Oct 10-12, 2017
Featured: SPTechCon, SharePoint Technology Conference, Washington, DC, Nov 12-15, 2017
Featured: Women in STEM Conference and Award, San Francisco, Sept 10-12, 2017
Featured: PrecisionAg Vision Conference, Phoenix, Oct 10-12, 2017
Featured: SPTechCon, SharePoint Technology Conference, Washington, DC, Nov 12-15, 2017
San Francisco Professional Events List
Please wait...
Things To Do Immediately About Master Validation Plan 2021
Date
Jan 29, 2021 - 09:00 AM
Link to Website
Organizer
Netzealous LLC DBA - Compliance4All
Venue
online
Location
161 Mission Falls Lane, Suite 216,,
Fremont,
California,
USA,
ZIP: 94539
Phone: 8004479407
Overview:
How to develop or improve upon a Master Verification and Validation Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements.
Why should you Attend:
The billions of dollars spent by industry annually for V&V are not providing the product safety or efficacy seemingly promised. For most companies, the fixes are not rocket-science, but proper up-front V&V planning and execution, documented in a corporate MVP and implemented by other V&V documents.
Areas Covered in the Session:
The 11 key documents for software validation
Incorporating 21 CFR Part 11 requirements
Suggested "test case" formats
Who Will Benefit:
Engineering
Production
Operations
Senior Management in Drugs
Speaker Profile:
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
How to develop or improve upon a Master Verification and Validation Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements.
Why should you Attend:
The billions of dollars spent by industry annually for V&V are not providing the product safety or efficacy seemingly promised. For most companies, the fixes are not rocket-science, but proper up-front V&V planning and execution, documented in a corporate MVP and implemented by other V&V documents.
Areas Covered in the Session:
The 11 key documents for software validation
Incorporating 21 CFR Part 11 requirements
Suggested "test case" formats
Who Will Benefit:
Engineering
Production
Operations
Senior Management in Drugs
Speaker Profile:
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses.
Event Fee: One Dial-in One Attendee Price: US $290.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
Event Categories
Keywords: Educational, technology , training