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The requirement for QP oversight has been extended to material for use in clinical trials since the introduction of EU Directive 2001/20/EC. In countries that are part of the Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S), the same role may be termed responsible person ( RP ) or authorized person ...
Volume 2C deals with Guidelines. Volume 3 - Guidelines. ... Eudralex,The Rules Governing Medicinal Products in the European Union, European Communities Commission ...
The European regulatory authorities update the database continuously and expect it to grow extensively over the next few years as more “GMP certificates are imported each year.” [2] The database serves as a quick reference for checking the good manufacturing practice (GMP) of a potential contract manufacturer.
In the UK, computer validation is covered in Annex 11 of the EU GMP regulations (EMEA 2011). The FDA introduced 21 CFR Part 11 for rules on the use of electronic records, electronic signatures (FDA 1997). The FDA regulation is harmonized with ISO 8402:1994, [6] which treats "verification" and "validation" as separate and distinct terms.
The company behind Los Angeles' emergency alert technology said it has added safeguards to prevent further inaccurate wildfire evacuation alerts from being sent to residents amid deadly ...
Good manufacturing practice guidelines provide guidance for manufacturing, testing, and quality assurance in order to ensure that a manufactured product is safe for human consumption or use. Many countries have legislated that manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation.
Preeclampsia is a high blood pressure condition that develops during pregnancy. Here's what you should know.
Dry January involves going alcohol-free for the first month of the year. Experts explain how giving up alcohol can improve your health.