Quality management of drug non-clinical research

Quality management of drug non-clinical research, Total:5 items.

The international standard classification for "Quality management of drug non-clinical research" includes: .

The Chinese standard classification for "Quality management of drug non-clinical research" includes: .

IX-EU/EC

• 1999/11/EC-1999 Commission Directive Adapting to Technical Progress the Principles of Good Laboratory Practice as Specified in Council Directive 87/18/EEC on the Harmonisation of Laws, Regulations and Administrative Provisions Relating to the Application of the Principle
• 2004/9/EC-2004 DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on the inspection and verification of good laboratory practice (GLP) (Codified version; Text with EEA relevance)
• COM(2002) 529 FINAL-2002 Proposal for a DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on the inspection and verification of good laboratory practice (GLP)(codified version)
• COM(2002) 530 FINAL-2002 Proposal for a DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applicat
• 2004/10/EC-2004 DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applications for tests

Others: Quality management of drug non-clinical research,The content of drug non-clinical research