Investigation of Out-of-Specification Test Results

  • Check with publisher
  • Published date: June 26, 2021
    • san Jose, california, United States

Attendees will learn how to streamline and conduct timely OOS and OOT investigations that meet FDA GMP expectations.

Responsibility of the Analyst
Responsibility of the Supervisor
Obvious error
Retesting
Resampling
Result validation
Initiation of a production investigation.
Invalidation of the initial result and accept the retest result.

Result 0 votes
Ashutos Swain
0 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • Human Error Reduction in GMP Manufacturing

    Human Error Reduction in GMP Manufacturing

    Pharmacology - Drug Development san Jose (california) June 25, 2021 Check with publisher

    Human error is known to be the major cause of observations from regulatory agencies, quality deviations, and production losses in many organizations. Although it is unlikely that human error will ever be totally eliminated, many human performance pro...

  • Writing and Revising SOPs for Increased Operational Efficiency

    Writing and Revising SOPs for Increased Operational Efficiency

    Pharmacology - Drug Development san Jose (california) May 24, 2021 Check with publisher

    Are new staff confused during training on your SOPs? Do you have too many SOPs? Do some SOPs give directions that conflict with directions from other SOPs? Are you writing up deviations far too often? Do you have some SOPs that just plainly don’t mak...

  • The Drug Development Process from Concept to Market

    The Drug Development Process from Concept to Market

    Pharmacology - Drug Development san Jose (california) May 22, 2021 Check with publisher

    This course is designed to cater for employees of pharmaceutical companies who would like an understanding of the drug development and regulatory approval process. The course starts by considering the global pharmaceutical market, important therapeut...