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  2. Cleaning validation - Wikipedia

    en.wikipedia.org/wiki/Cleaning_validation

    Cleaning validation is the methodology used to assure that a cleaning process removes chemical and microbial residues of the active, inactive or detergent ingredients of the product manufactured in a piece of equipment, the cleaning aids utilized in the cleaning process and the microbial attributes.

  3. Validation master plan - Wikipedia

    en.wikipedia.org/wiki/Validation_master_plan

    A VMP is the foundation for the validation program and should include process validation, facility and utility qualification and validation, equipment qualification, cleaning and computer validation. It is a key document in the GMP ( Good manufacturing practice ) regulated pharmaceutical industry as it drives a structured approach to validation ...

  4. Verification and validation - Wikipedia

    en.wikipedia.org/wiki/Verification_and_validation

    Verification is intended to check that a product, service, or system meets a set of design specifications. [6] [7] In the development phase, verification procedures involve performing special tests to model or simulate a portion, or the entirety, of a product, service, or system, then performing a review or analysis of the modeling results.

  5. File:Male Masturbation with Ejaculation Video.webm - Wikipedia

    en.wikipedia.org/wiki/File:Male_Masturbation...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  6. Reading Scientific Services - Wikipedia

    en.wikipedia.org/wiki/Reading_Scientific_Services

    Reading Scientific Services Ltd. (RSSL) is a British company that provides scientific analysis, consultancy, product development and training to the global food, drink, healthcare, pharmaceutical, biopharmaceutical and consumer goods sectors. It has been inspected by regulatory authorities including the U.S. Food and Drug Administration, the ...

  7. Validation (drug manufacture) - Wikipedia

    en.wikipedia.org/wiki/Validation_(drug_manufacture)

    It is the foundation for the validation program and should include process validation, facility and utility qualification and validation, equipment qualification, cleaning and computer validation. The regulations also set out an expectation that the different parts of the production process are well defined and controlled, such that the results ...

  8. Army sec nominee questions whether military pilots should ...

    www.aol.com/army-sec-nominee-questions-whether...

    Army secretary nominee Daniel Driscoll questioned whether Army helicopters should be flying training missions in one of the nation’s most congested flight paths after Wednesday's tragic ...

  9. Clean-in-place - Wikipedia

    en.wikipedia.org/wiki/Clean-in-place

    Contact time of the cleaning solution. The longer the detergent contact period, the higher the cleaning efficiency. After some time, the detergent eventually dissolves the hard stains/soil from the dirty surface. Pressure exerted by the cleaning solution (or turbulence). The turbulence creates an abrasive force that dislodges stubborn soil from ...