Equipment and QMS Software by Verification Process

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Category R&D, Engineering, Production, Operations

Deadline: March 07, 2017 | Date: March 08, 2017

Venue/Country: Online Event, U.S.A

Updated: 2017-01-16 20:26:30 (GMT+9)

Call For Papers - CFP

The FDA and other regulatory agencies have stated that software validation can only be accomplished effectively if "risk-based".How can this be done in the "real world".

Why should you Attend:

Software has become pervasive in medical devices themselves, and in the controlling, running and monitoring of medical product processes, whether they be in the pharmaceutical, medical device, biologics or dietary supplements industries. A quick review of Internet forums will show much confusion about the subject.

Areas Covered in the Session:

Verification or Validation-FDA Expectations

The Project V&V Plan

An FDA-accepted Documentation "Model"

Product and Process/Test Facilities/Equipment Software V&V

Who Will Benefit:

Senior management in Drugs,Devices,Combination Products,Biologics,Dietary Supplements

QA / RA

Software development,Programming,Documentation,Testing teams

R&D

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.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com