enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Critical process parameters - Wikipedia

    en.wikipedia.org/wiki/Critical_Process_Parameters

    Critical process parameters (CPP) in pharmaceutical manufacturing are key variables affecting the production process. CPPs are attributes that are monitored to detect deviations in standardized production operations and product output quality or changes in critical quality attributes .

  3. Process validation - Wikipedia

    en.wikipedia.org/wiki/Process_Validation

    Process analytical technology is used to measure critical process parameters (CPP) and critical quality attributes (CQA). PAT facilitates measurement of quantitative production variables in real time and allows access to relevant manufacturing feedback.

  4. Process analytical technology - Wikipedia

    en.wikipedia.org/wiki/Process_analytical_technology

    Process analytical technology (PAT) has been defined by the United States Food and Drug Administration (FDA) as a mechanism to design, analyze, and control pharmaceutical manufacturing processes through the measurement of critical process parameters (CPP) which affect the critical quality attributes (CQA).

  5. Certificate of pharmaceutical product - Wikipedia

    en.wikipedia.org/wiki/Certificate_of...

    The certificate of pharmaceutical product (abbreviated: CPP) is a certificate issued in the format recommended by the World Health Organization (WHO), which establishes the status of the pharmaceutical product and of the applicant for this certificate in the exporting country; [1] it is often mentioned in conjunction with the electronic Common Technical Document (eCTD).

  6. Certified Quality Auditor - Wikipedia

    en.wikipedia.org/wiki/Certified_Quality_Auditor

    A Certified Quality Auditor (CQA) is a professional that knows and employs the standards and principles associated with auditing. A CQA is capable of using various evaluation techniques to identify a production system 's strengths and weaknesses in quality control .

  7. Compatibility of C and C++ - Wikipedia

    en.wikipedia.org/wiki/Compatibility_of_C_and_C++

    This article, however, focuses on differences that cause conforming C code to be ill-formed C++ code, or to be conforming/well-formed in both languages but to behave differently in C and C++. Bjarne Stroustrup , the creator of C++, has suggested [ 4 ] that the incompatibilities between C and C++ should be reduced as much as possible in order to ...

  8. 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.

  9. List of professional designations in the United States

    en.wikipedia.org/wiki/List_of_professional...

    CPP: ASIS International, International Foundation for Protection Officers: Certified Protection Executive CPE National Protective Services [127] Certified Protection Officer: CPO: International Foundation for Protection Officers: Certified in Security Supervision and Management: CSSM: International Foundation for Protection Officers