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Medication Self-Administration Trial

Medication Self-Administration Trial, Total:9 items.

In the international standard classification, Medication Self-Administration Trial involves: Pharmaceutics, Terminology (principles and coordination).

KR-KS, Medication Self-Administration Trial

• KS P ISO 15197-2017(2022) In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

农业农村部, Medication Self-Administration Trial

• NY/T 1860.37-2016 Test Guidelines for Determination of Physical and Chemical Properties of Pesticides Part 37: Testing of Self-Heating Substances

Hunan Provincial Standard of the People's Republic of China, Medication Self-Administration Trial

• DB43/T 2135-2021 Technical Service Specifications for the Recruitment and Management of Drug Clinical Trial Subjects

Group Standards of the People's Republic of China, Medication Self-Administration Trial

• T/SHQAP 001-2023 Guidelines for the Construction of Quality Management Systems for Drug Clinical Trial Sponsors

Military Standard of the People's Republic of China-Commission of Science,Technology and Industry for National Defence, Medication Self-Administration Trial

• GJB 5382.11-2005 Test methods of physical parameter for pyrotechnic. Part 11: Determination of Autoignition temperature. DTA and DSC method

Military Standard of the People's Republic of China-General Armament Department, Medication Self-Administration Trial

• GJB 8683.11-2015 Test methods for physical parameters of pyrotechnics Part 11: Determination of spontaneous ignition temperature Differential thermal analysis and differential scanning calorimetry

IX-EU/EC, Medication Self-Administration Trial

• 2001/20/EC-2001 Directive of the European Parlament and of the Council on the Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Practice in the Conduct of Clinical Trials on Medicinal
• 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
• COM(1999) 193 FINAL-1999 Amended Proposal for a European Parliament and Council Directive on the Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Parctice in the Conduct of Clinical Trials on

Others:   drug test, drug trial data, drug metabolism test, drug metabolism test, drug compatibility test, drug trials, Medication Self-Administration Trial, Overseas Drug Clinical Trials, drug compatibility test, drug test, experimental drug, Drug Clinical Trials, Drug Clinical Trials, drug stability test, Drug Clinical Trial License, experimental drug, drug penetration test, drug sensitivity test, Classification of experimental drugs, drug toxicity test.