Showing items related by title, author, creator and subject.

• Code of Practice for the Clinical Assessment of Licensed Medicinal Products in General Practice 

  Unknown author (British Medical Association; Royal College of General Practitioners; Association of the British Pharmaceutical Industry, 1983-04-16)

  A code of practice for the clinical assessment of licensed drugs by physicians in general practice has been developed jointly by the British Medical Association, the Royal Society of General Practitioners, and the Association ...
• International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Adopts Consolidated Guideline on Good Clinical Practice in the Conduct of Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use 

  Unknown author (1997)
• Draft Commission Directive Laying Down Principles and Detailed Guidelines for Good Clinical Practice as Regards Investigational Medicinal Products for Human Use, as Well as the Requirements for Authorisation of Manufacturing or Importation Of Such Products 

  Unknown author (European Commission, 2004-06-14)

  This proposed directive redrafts the original European Union clinical trials directive (2001/20/EC) that was developed to govern approval and monitoring of commercially-sponsored clinical research in countries of the ...