FDAnews Management Report: Devicemaker’s Guide to Process Validation

Devicemaker’s Guide to Process Validation

Falls Church, VA (PRWEB) November 13, 2013

Devicemaker’s Guide to Process Validaiton

**FDAnews Management Report**


Time hasn’t stood still on the manufacturing floor: New and more complex manufacturing processes emerge every year, greater outsourcing leaves devicemakers relying more on third-party manufacturers, and international standards continue evloving. Devicemakers need to be sure their process validation systems have kept pace with reality.

This management report takes readers step-by-step through the most complex, challenging process validation compliance problems, filling in the gaps left in the available guidance. Among questions it addresses and resolves:

    What processes should be validated? The simplified decision tree included in this report removes all questions
    If a company uses sampling plans in lieu of a validated process, what percentage of sampling is adequate? Discover how the FDA has addressed this issue in warning letters
    When the GHTF talks about operation qualification, does it mean the same as when the FDA talks about operational qualification? The report includes a simple crosswalk that clarifies the FDA’s meaning

Discover specific solutions to issues and questions that bedevil many devicemakers. The report includes:

    An overview of the existing requirements for process validation from the Quality Systems Regulation and Quality Systems Manual
    How the FDA inspects devicemakers for process validation compliance
    Latest thinking of international and US regulators on process validation approaches contained in GHTF guidelines
    Lessons from warning letters on the FDA’s evolving expectations for process validation
    And much more

Order today.

Lacking specific new guidance, FDA’s intentions for process validation must be identified through warning letters, official statements and official documents. FDAnews has done the hard work for you. Until CDRH issues its long-awaited guidance, Devicemaker’s Guide to Process Validation will keep devicemakers in compliance.

Devicemaker’s Guide to Process Validaiton

**FDAnews Management Report**


FORMAT: Print or PDF

PRICE: $ 377


Online:     http://www.fdanews.com/ProcessValidation

By phone: 888-838-5578 or 703-538-7600


FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews’ print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA’s complex and ever-changing regulations.


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