Thursday, May 3, 2018

FDA 21 CFR Part 11 Compliance – Validation Seminar 2018 (Washington DC, United States, June 28-29, 2018) – ResearchAndMarkets.com | Business

DUBLIN–(BUSINESS WIRE)–May 2, 2018–The “FDA 21 CFR Part 11 Compliance – Validation Seminar 2018” training has been added to ResearchAndMarkets.com’s offering.

Part 11 / Annex 11 Computer Systems Validation (CSV) is implemented in order to increase the integrity, accountability and security of the spreadsheets and achieve GxP Compliance. CSV enables the level and rigor of specification and verification applied to spreadsheets to be based on spreadsheet risk, complexity, and novelty. This hands-on seminar will provide the attendees with the tools for successful computer systems validation for Excel Spreadsheets.

Spreadsheets are a very powerful and useful tool in the GxP environment especially when coupled with the fact that it is easy to build spreadsheet applications without much training. However, this results in spreadsheets being among the most under-documented systems used in GxP environments because:

Users regard them as part of the desktopThe ease with which applications can be built without much trainingThe data processing power that they can haveLack of knowledge that spreadsheets need to be validatedLack of knowledge on how to validate spreadsheets

Consequently, Spreadsheets have become low hanging fruit during FDA or other regulatory inspections and many warning letters have been issued.

Agenda

Day 1 Schedule

Lecture 1: Types of SpreadsheetsLecture 2: Excel Validation at a High LevelLecture 3: FDA Use of Excel SpreadsheetsLecture 4: Excel Validation Master Plan (VaMP)

Day 2 Schedule

Lecture 5: Excel Risk Assessment & RequirementsLecture 6: Excel Functional & Design SpecificationLecture 7: Verification & Testing for Excel CSVLecture 8: Quality Assurance for Excel CSV

For more information about this training visit https://www.researchandmarkets.com/research/wnfbcg/fda—21—cfr—part?w=4

View source version on businesswire.com:https://ift.tt/2rgnGni

CONTACT: ResearchAndMarkets.com

Laura Wood, Senior Manager

press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470

For U.S./CAN Toll Free Call 1-800-526-8630

For GMT Office Hours Call +353-1-416-8900

Related Topics:Pharmaceuticals,Drug Discovery,Pharmaceutical Manufacturing

KEYWORD:

INDUSTRY KEYWORD: HEALTH PHARMACEUTICAL

SOURCE: Research and Markets

Copyright Business Wire 2018.

PUB: 05/02/2018 03:31 PM/DISC: 05/02/2018 03:31 PM

https://ift.tt/2Kyww8Y

Copyright Business Wire 2018.

Source link

No comments:

Pharmaceutical Validation Documentation Requirements

Pharmaceutical validation is a critical process that ensures that pharmaceutical products meet the desired quality standards and are safe fo...