Good Manufacturing Practices . See

Good manufacturing practice See Quality system regulation. 

Current good manufacturer practice, see cGMP Cyanovirin 1406... 

In the pharmaceutical industry Good Manufacturing Practice (see also cGMP)... 

Directive 2001/83/EC points with Article 47 2nd paragraph at the Commission Directive 2003/94/EC laying down the principles and guidelines of good manufacturing practice (see Sect. 35.5.7) in respect of medicinal products for human use and investigational medicinal products for human use. In the introduction on GMP it is stated that... 

The manufacture of all investigational medicinal products (including placebo) that are intended for a clinical trial must be authorised and conducted according to Good Manufacturing Practice (GMP). This should be supervised and certified by a Qualified Person . An import authorisation is required for any product from outside the EU, which should also be manufactured to GMP standards. (See Ghapters 11 and 12 for information on GMP, manufacturing authorisations and Qualified Persons.)... 

See also Current good manufacturing practices (cGMPs)... 

LffiTAL SURFACE TREATMENTS - CHEMICALAND ELECTROCHEMICAL CONVERSION TREATMENTS] (Vol 16) GMP. See Current Good Manufacturing Practice. 

Validation Action of proving, in accordance with the principles of Good Manufacturing Practice, that any procedure, process, equipment, material, activity, or system actually leads to the expected results (see also qualification) (EU PIC/S). 

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