This Saturday’s edition of 21st Century Television focuses on software validation for FDA compliance and how meeting FDA regulatory requirements for software related to the use of medical devices is an important step in eliminating patient risk. 21st Century Television provides deep insights into the way the global economy is viewed by the actual businesspeople “in the trenches”, and how they have developed products and strategies to compete.
Scheduled for Saturday, May 3, 2014 at 4:30pm ET/ 1:30pm PT on the Fox Business Network as pd prog, this is one episode you won’t want to miss!
About 21st Century Television
21st Century Television is an award winning business and health program that is independently produced by MMP (USA), Inc. The show provides its viewers an in depth opportunity to find solutions to the industry problems from some of the top business leaders from across the world. With more than 5,000 companies participating on over 500 shows, 21st Century Television continues to be the premier and targeted outlet for the latest business and health stories. 21st Century Television airs on cable networks to over 100 million viewers.
For specific market-by-market air dates and times, please e-mail Moniqueh@mmpusa.com. For more information, please visit http://www.tvbusinessnews.com.
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Company Name:MMP (USA), Inc
Contact Person: Gila Stern
Email:gstern@mmpusa.com
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State: Florida
Country: United States
Website: http://tvbusinessnews.com/may-2014/fbn/21ctv2666-fbn.pdf
2 comments:
Focuses on the validation of laboratory equipments used in the production of pharmaceutical products.
Determination the requirements of the end user,
which are often defined in the User Requirements Specifications.Software validation is a part of the design validation for a finished device,
but is not separately defined in the Quality System regulation.
equipment validation
Validation has become one of the pharmaceutical industry’s most recognized and discussed subjects.
It is a critical success factor in product approval and ongoing commercialization.
This article provide brief introduction about the pharmaceutical process validation and its importance according to regulatory provision,
also provide the answer of question like why to do, when to do and how to do it.
This work is to present an introduction and general overview on process validation of pharmaceutical manufacturing process.
Quality is always an imperative prerequisite when we consider any product.
equipment validation
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