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human drug

human drug, Total:13 items.

In the international standard classification, human drug involves: Medical sciences and health care facilities in general, Pharmaceutics, Services, Applications of information technology.

RU-GOST R, human drug

• GOST R 56700-2015 Medicines for medical applications. Safety Pharmacology studies for human pharmaceuticals

US-FCR, human drug

• FCR 21 CFR PART 250-2015 SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
• FCR 21 CFR PART 250-2014 SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
• FCR 21 CFR PART 330-2014 OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED
• FCR 21 CFR PART 330-2013 OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED

GOSTR, human drug

• GOST R 58173-2018 Immunotoxicity investigations intended for humans pharmaceuticals

Group Standards of the People's Republic of China, human drug

• T/ZSP 004-2023 Operation guide for non-pharmacological intervention therapy for the elderly with dementia in nursing homes

CU-NC, human drug

• NC 26-135-03-1988 Drugs. Adults Composed Theophiline Suppósitories Quality Specifications
• NC 26-75-19-1985 Drugs. Freeze-dried Solvent for "Gonadotrofina Corionica" Human Injection Quality Specifications

British Standards Institution (BSI), human drug

• BS EN ISO 27953-2:2012 Health informatics. Individual case safety reports (ICSRs) in pharmacovigilance. Human pharmaceutical reporting requirements for ICSR
• BS EN ISO 27953-2:2011 Health informatics. Individual case safety reports (ICSRs) in pharmacovigilance - Human pharmaceutical reporting requirements for ICSR

American National Standards Institute （ANSI), human drug

• ANSI/HL7 V3 ICSRP 2, R 2-2012 HL7 Version 3 Standard: Pharmacovigilance - Individual Case Safety Report, Part 2: Human Pharmaceutical Reporting Requirements for ICSR, R2

International Organization for Standardization (ISO), human drug

• ISO/HL7 27953-2:2011 Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 2: Human pharmaceutical reporting requirements for ICSR

Others:   people, Prion for everyone, Prion for everyone, human drug, Prion + Everyone, rat man, Imaging people, American, program person, human environment, people extract, Thousand Talents Program, Experiment everyone, everyone, experiment for everyone, Hundred people plan, Hominid, L-drugs D-drugs, others, human chemical drug.