Procedural assessments of SOPs to ensure SOPs are logical and meet GXP requirements [electronic resource] / Susan Ollier.

By: Ollier, Susan [spk]Contributor(s): Wilson, Pam. (QED Clinical Services, UK) [spk]Material type: FilmFilmSeries: Henry Stewart talksBiomedical & life sciences collection. SOPs for regulatory applications for the pharmaceutical industry: Publisher: London : Henry Stewart Talks, 2013Description: 1 online resource (1 streaming video file (33 min.) : color, sound)Other title: Procedural assessments of standard operating procedures to ensure standard operating procedures are logical and meet GXP requirementsSubject(s): Communication of technical information | Pharmaceutical industry -- Documentation -- Standards | Pharmaceutical industry -- Quality control -- Documentation | Quality control -- Documentation | Drug Industry -- methods | Drug Industry -- organization & administration | Drug Industry -- standards | Guideline Adherence -- organization & administration | Guidelines as Topic | Quality Control -- methodsOnline resources: Click here to access online | Series
Contents:
Contents: Procedural assessment cycle and tools of SOPs -- Working instruction template -- The SOP title -- The scope of content -- When scope covers multiple tasks or is a part of a larger process -- Filling the scope, procedure & checklist in our template -- Authors, general requirements and further elements of content -- Importance of up-to-date information -- Proper writing & revising of the content -- Preparing a checklist -- Regulatory requirements -- Sources of information -- Documentation -- Format and language -- Points to remember -- Added value -- Feasibility.
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Animated audio-visual presentation with synchronized narration.

Title from title frames.

Contents: Procedural assessment cycle and tools of SOPs -- Working instruction template -- The SOP title -- The scope of content -- When scope covers multiple tasks or is a part of a larger process -- Filling the scope, procedure & checklist in our template -- Authors, general requirements and further elements of content -- Importance of up-to-date information -- Proper writing & revising of the content -- Preparing a checklist -- Regulatory requirements -- Sources of information -- Documentation -- Format and language -- Points to remember -- Added value -- Feasibility.

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