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According to medical research

According to medical research, Total:124 items.

In the international standard classification, According to medical research involves: Medical sciences and health care facilities in general, Quality, Pharmaceutics, Road engineering, Standardization. General rules, Sociology. Demography, Test conditions and procedures in general, Applications of information technology, Laboratory medicine, Farming and forestry, Microbiology, Medical equipment, Interface and interconnection equipment, Biology. Botany. Zoology.

US-FCR, According to medical research

FCR FED H-08-9 CHAP 278-1983 MEDICAL RESEARCH AND DEVELOPMENT
FCR FED H-08-5 CHAP 278 TRANSMITTAL NO.177-1986 MEDICAL RESEARCH AND DEVELOPMENT, TRANSMITTAL NO. 177
FCR COE ETL 1110-1-154-1994 STANDARD OUTLINES FOR SCOPES-OF-WORK FOR INVESTIGATIONS AND STUDIES AT HAZARDOUS, TOXIC, AND RADIOACTIVE WASTE (HTRW) SITES UNDER CERCLA (SARA), RCRA, AND NEPA

Group Standards of the People's Republic of China, According to medical research

T/NAHIEM 6-2018 General Requirements of Medical ethics committee
T/CACM 1323-2019 Technical Specifications for Supervision of Clinical Research Data of Traditional Chinese Medicine
T/CACM 1335.3-2020 Standardized Operating Procedures for Overall Evidence Research in Traditional Chinese Medicine Part 3: Combing of Modern Research Evidence
T/GDPHA 015-2021 Data Element Standard for Clinical Scientific Research of Live Cancer
T/GDPHA 016-2021 Data Element Standard for Clinical Scientific Research of Gastric Cancer
T/GDPHA 014-2021 Data Element Standard for Clinical Scientific Research of Lung Cancer
T/GDPHA 012-2021 Data Element Standard for Clinical Scientific Research of Diabetes
T/GDPHA 005-2021 Data Element Standard for Clinical Scientific Research of Cerebral Hemorrhage
T/GDPHA 020-2021 Data Element Standard for Clinical Scientific Research of Mammary cancer
T/GDPHA 011-2021 Data Element Standard for Clinical Scientific Research of Anxiety Disorder
T/GDPHA 017-2021 Data Element Standard for Clinical Scientific Research of Esophageal Cancer
T/GDPHA 004-2021 Data Element Standard for Clinical Scientific Research of Cerebral Infarction
T/GDPHA 003-2021 Data Element Standard for Clinical Scientific Research of Coronary Heart Disease
T/GDPHA 008-2021 Data Element Standard for Clinical Scientific Research of Depression
T/GDPHA 006-2021 Data Element Standard for Clinical Scientific Research of Autism
T/GDPHA 019-2021 Data Element Standard for Clinical Scientific Research of Pancreatic Cancer
T/GDPHA 018-2021 Data Element Standard for Clinical Scientific Research of Colorectall Cancer
T/GDPHA 002-2021 Data Element Standard for Clinical Scientific Research of Hypertension
T/GDPHA 001-2021 Data Element Standard for Clinical Scientific Research of Chronic Diseases
T/GDPHA 021-2021 Data Element Standard for Clinical Scientific Research of Malignant Lymphoma
T/GDPHA 025-2021 Data Element Standard for Clinical Scientific Research of Diabetes
T/GDPHA 009-2021 Data Element Standard for Clinical Scientific Research of Schizophrenia
T/GDPHA 010-2021 Data Element Standard for Clinical Scientific Research of Bipolar Disorder
T/GDPHA 007-2021 Data Element Standard for Clinical Scientific Research of Alzheimer's Disease
T/CACM 1335.1-2020 Standardized operating procedures for integral evidence research of traditional Chinese medicine part 1: general principles
T/CACM 1335.2-2020 Standardized Operating Procedures for Overall Evidence Research of Traditional Chinese Medicine Part 2: Combing the Evidence from Ancient Books
T/GDPHA 013-2021 Data Element Standard for Clinical Scientific Research of Chronic Obstructive Pulmonary Disease

National Aeronautics and Space Administration (NASA), According to medical research

NASA NPD 8900.3 REV H-2011 ASTRONAUT MEDICAL AND DENTAL OBSERVATION STUDY AND CARE PROGRAM

Canadian General Standards Board （CGSB), According to medical research

CAN/CGSB-191.1-2013 Research ethics oversight of biomedical clinical trials

GB-REG, According to medical research

REG 7 CFR PART 2812-2012 DEPARTMENT OF AGRICULTURE GUIDELINES FOR THE DONATION OF EXCESS RESEARCH EQUIPMENT UNDER 15 U.S.C. 3710(i)
REG NASA-LLIS-2156-2010 Lessons Learned - Use of Research and Education Networks (RENS) for Science Data Transfer

RU-GOST R, According to medical research

GOST R 56700-2015 Medicines for medical applications. Safety Pharmacology studies for human pharmaceuticals
GOST R 56702-2015 Medicines for medical applications. Nonclinical toxicology and pharmacokinetic studies of safety
GOST R ISO 14199-2016 Health informatics. Information models. Biomedical Research Integrated Do-main Group (BRIDG) Model
GOST ISO 10993-16-2016 Medical devices. Biological evaluation of medical devices. Part 16. Toxicokinetic study design for degradation products and leachables
GOST R ISO 10993.16-1999 Medical devices. Biological evaluation of medical devices. Part 16. Toxicokinetic study design for degradation products and leachables
GOST ISO 10993-16-2011 Medical devices. Biological evaluation of medical devices. Part 16. Toxicokinetic study design for degradation products and leachables

Guangdong Provincial Standard of the People's Republic of China, According to medical research

DB4403/T 86-2020 Code of Ethics Review for Biomedical Research Involving Humans

Hunan Provincial Standard of the People's Republic of China, According to medical research

DB43/T 2561-2023 Code of Ethics Review for Biomedical Research Involving Humans

Shanghai Provincial Standard of the People's Republic of China, According to medical research

DB31/T 899-2015 Code of Ethics Review for Biomedical Research Involving Humans

International Organization for Standardization (ISO), According to medical research

ISO 14199:2015 Health informatics - Information models - Biomedical Research Integrated Domain Group (BRIDG) Model
ISO/DIS 14199 Health informatics — Information models — Biomedical Research Integrated Domain Group (BRIDG) Model
ISO/TR 10993-55:2023 Biological evaluation of medical devices — Part 55: Interlaboratory study on cytotoxicity
ISO 10993-16:2010 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
ISO 10993-16:2017 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
ISO/TR 23358:2022 Health informatics — A case study on establishing standardized measurement data in cardiac examination reports
ISO/DTS 9491-1 Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models
ISO/TS 9491-1:2023 Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models
ISO/TS 11796:2023 Biological evaluation of medical devices — Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices

British Standards Institution (BSI), According to medical research

BS ISO 14199:2015 Health informatics. Information models. Biomedical Research Integrated Domain Group (BRIDG) Model
BS EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Clinical investigation plans
PD ISO/TR 10993-55:2023 Biological evaluation of medical devices. Interlaboratory study on cytotoxicity
BS EN ISO 14155:2011 Clinical investigation of medical devices for human subjects. Good clinical practice
23/30461124 DC BS ISO 14199. Health informatics. Information models. Biomedical Research Integrated Domain Group (BRIDG) Model
BS EN ISO 10993-16:2017 Biological evaluation of medical devices - Toxicokinetic study design for degradation products and leachables
BS EN ISO 10993-16:2010 Biological evaluation of medical devices - Toxicokinetic study design for degradation products and leachables
BS EN ISO 10993-16:1997 Biological evaluation of medical devices - Toxicokinetic study design for degradation products and leachables
PD ISO/TR 23358:2022 Health informatics. A case study on establishing standardized measurement data in cardiac examination reports
PD ISO/TS 9491-1:2023 Biotechnology. Predictive computational models in personalized medicine research. Constructing, verifying and validating models
PD 6632:1998 Biotechnology. Laboratories for research, development and analysis. Guidance on the selection of equipment needed for biotechnology laboratories according to the degree of hazard
BS ISO 20916:2019 In vitro diagnostic medical devices. Clinical performance studies using specimens from human subjects. Good study practice

European Committee for Standardization (CEN), According to medical research

EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
EN ISO 10993-16:2010 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

API - American Petroleum Institute, According to medical research

API PUBL 4494 VOL II-1989 Monitoring near Refineries for Airborne Chemicals on the SARA Title III Section 313 List Volume II A Generic Study Design Protocol
API 26-60117- CHAPTER III: EXPERIMENTS IN HUMAN WORK CAPABILITIES UNDER PRESSURE@ NOW BEING CONDUCTED AT THE INSTITUTE FOR ENVIRONMENTAL MEDICINE@ UNIVERSITY OF PENNSYLVANIA (Best Copy Available)

German Institute for Standardization, According to medical research

DIN 58959-4:1997-06 Quality management in medical microbiology - Part 4: Requirements for investigations using light microscopes / Note: To be replaced by DIN 58959-6 Beiblatt 2 (2021-08, t).
DIN 58959-19:1997 Quality management in medical microbiology - Part 19: Requirements for the use of control strains for the examination of fungi
DIN 58959-18:1997 Quality management in medical microbiology - Part 18: Requirements for the use of control strains for the examination of mycoplasms
DIN 58959-17:1997 Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria
DIN EN ISO 10993-16:2018-02 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017); German version EN ISO 10993-16:2017
DIN EN ISO 10993-16:2018 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
DIN 58959-20:1997 Quality management in medical microbiology - Part 20: Requirements for the use of control material for the examination of protozoae and microorganisms of higher order

CU-NC, According to medical research

NC 20-06-24-1987 Medical Sciences. Electrolytic and Basic Acid Equilibrium Study. Determination of Ion Potassium Concentration. Chemical Analysis Method

Shanxi Provincial Standard of the People's Republic of China, According to medical research

DB14/T 2857-2023

International Telecommunication Union (ITU), According to medical research

ITU-T SERIES J SUPP 11-2021 Guidelines for installing a digital television service for cable networks based on ITU-T Recommendations (Study Group 9)
ITU-T V.16-1988 MEDICAL ANALOGUE DATA TRANSMISSION MODEMS
ITU-T K.63-2004 Maintaining the suitability of production telecommunications equipment to its intended electromagnetic environment SERIES K: PROTECTION AGAINST INTERFERENCE Study Group 5
ITU-T X.1092-2013 Integrated framework for telebiometric data protection in e-health and telemedicine (Study Group 17)
ITU-T D.41-1989 INTRODUCTION OF ACCOUNTING RATES BY ZONES IN THE INTERNATIONAL PUBLIC TELEGRAM SERVICE

ITU-T - International Telecommunication Union/ITU Telcommunication Sector, According to medical research

ITU-T R.11-1989 Calculation of the Degree of Distortion of a Telegraph Circuit in Terms of the Degrees of Distortion of the Component Links - Telegraph Transmission (Study Group IX) 2 pp
ITU-T P.78-1989 Subjective Testing Method for Determination of Loudness Ratings in Accordance with Recommendation P.76 - Telephone Transmission Quality (Study Group XII) 17 pp
ITU-T U.15-1989 Interworking Rules for International Signalling Systems According to Recommendations U.1@ U.11 and U.12 - Telegraph Switching (Study Group IX) 8 pp
ITU-T X.28 ADD 1-1994 Addendum 1 to Recommendation X.28 to Enable Map Support in Accordance with Recommendation X.8 - Data Networks and Open System Communications Public Data Networks - Interfaces (Study Group 7; 11 pp)
RECMN X.28 ADD 1-1994 Addendum 1 to Recommendation X.28 to Enable Map Support in Accordance with Recommendation X.8 - Data Networks and Open System Communications Public Data Networks - Interfaces (Study Group 7) 11 pp
ITU-T K.133-2018 Electromagnetic environment of body-worn equipment in the 2.4 GHz and 13.56 MHz industrial@ scientific and medical band (Study Group 5)
ITU-T G.9992-2019 Indoor optical camera communication transceivers – System architecture@ physical layer and data link layer specification (Study Group 15)
ITU-T P.78-1993 Subjective Testing Method for Determination of Loudness Ratings in Accordance with Recommendation P.76 - Telephone Transmission Quality Measurements Related to Speech Loudness (Study Group XII) 19 pp

Korean Agency for Technology and Standards (KATS), According to medical research

KS P ISO 10993-16:2017 Biological evaluation of medical devices — Part16:Toxicokinetic study design for degradation products and leachables
KS P ISO 10993-16:2006 Biological evaluation of medical devices－Part 16：Toxicokinetic study design for degradation products and leachables
KS P ISO 10993-16:2021 Biological evaluation of medical devices —Part 16: Toxicokinetic study design for degradation products and leachables

KR-KS, According to medical research

KS P ISO 10993-16-2017 Biological evaluation of medical devices — Part16:Toxicokinetic study design for degradation products and leachables
KS P ISO 10993-16-2021 Biological evaluation of medical devices —Part 16: Toxicokinetic study design for degradation products and leachables

国家市场监督管理总局、中国国家标准化管理委员会, According to medical research

GB/T 16886.16-2021 Biological evaluation of medical devices—Part 16: Toxicokinetic study design for degradation products and leachables

US-AAMI, According to medical research

ANSI/AAMI/ISO 10993-16:2017 Biological evaluation of medical devices-Part 16: Toxicokinetic study design for degradation products and leachables

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, According to medical research

GB/T 16886.16-2013 Biological evaluation of medical devices.Part 16: Toxicokinetic study design for degradation products and leachables
GB/T 16886.16-2003 Biological evaluation of medical devices--Part 16: Toxicokinetic study design for degradation products and leachables

未注明发布机构, According to medical research

BS EN ISO 10993-16:2017(2020) Biological evaluation of medical devices Part 16 : Toxicokinetic study design for degradation products and leachables

TH-TISI, According to medical research

TIS 2395.16-2008 Biological evaluation of medical devices.part 16: toxicokinetic study design for degradation products and leachables

ES-UNE, According to medical research

UNE-EN ISO 10993-16:2018 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

Association Francaise de Normalisation, According to medical research

NF EN ISO 10993-16:2017 Évaluation biologique des dispositifs médicaux - Partie 16 : conception des études toxicocinétiques des produits de dégradation et des substances relargables
NF EN 60335-2-95:2017 Évaluation biologique des dispositifs médicaux - Partie 16 : conception des études toxicocinétiques des produits de dégradation et des substances relargables
NF S99-501-16*NF EN ISO 10993-16:2017 Biological evaluation of medical devices - Part 16 : Toxicokinetic study design for degradation products and leachables
NF S99-501-16:2010 Biological evaluation of medical devices - Part 16 : toxicokinetic study design for degradation products and leachables.
FD X42-205*FD CR 12739:1999 Biotechnology. Laboratories for research, development and analysis. Report on the selection of equipment needed for biotechnology laboratories according to the degree of hazard.
FD CR 12739:1999 Biotechnologie - Laboratoires de recherche, développement et analyse - Rapport sur le choix des équipements nécessaires dans les laboratoires de biotechnologie en fonction du degré de danger.
NF S99-516:1997 Biological evaluation of medical devices. Part 16 : toxicokinetic study design for degradation products and leachables.

Institute of Electrical and Electronics Engineers (IEEE), According to medical research

IEEE P1584.1/D5, January 2021 IEEE Draft Guide for the Specification of Scope and Deliverable Requirements for an Arc-Flash Hazard Calculation Study in Accordance with IEEE Std 1584(TM)
P1584.1/D7, January 2022 IEEE Draft Guide for the Specification of Scope and Deliverable Requirements for an Arc-Flash Hazard Calculation Study in Accordance with IEEE Std 1584(TM)

IX-EU/EC, According to medical research

2008/345/EC-2008 COMMISSION RECOMMENDATION on a code of conduct for responsible nanosciences and nanotechnologies research
2007/678/EC-2007 COMMISSION DECISION amending Decision 2004/452/EC laying down a list of bodies whose researchers may access confidential data for scientific purposes

CEN - European Committee for Standardization, According to medical research

EN ISO 10993-16:2017 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
EN ISO 10993-16:2009 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

IAEA - International Atomic Energy Agency, According to medical research

WS-G-2.7-2005 Management of Waste from the Use of Radioactive Material in Medicine@ Industry@ Agriculture@ Research and Education

Conference of European Post Telecommunication (CEPT), According to medical research

CEPT ERC REPORT 29-1994 Compatibility Study between Mobile Satellite Service in the 1610-1626.5 MHz Band and Fixed Service Operating under RR730 (Brussels, June 1994)

Danish Standards Foundation, According to medical research

DS/CEN/CR 12739:1999 Biotechnology - Laboratories for research, development and analysis - Report on the selection of equipment needed for biotechnology laboratories according to the degree of hazard

VN-TCVN, According to medical research

TCVN 7391-16-2007 Biological evaluation of medical devices.Part 16: Toxicokinetic study design for degradation products and leachables

Taiwan Provincial Standard of the People's Republic of China, According to medical research

CNS 14393-16-2006 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

AENOR, According to medical research

UNE-EN ISO 10993-16:2010 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)
UNE-CR 12739:2000 BIOTECHNOLOGY. LABORATOIRES FOR RESEARCH, DEVELOPMENT AND ANALYSIS. REPORT ON THE SELECTION OF EQUIPMENT NEEDED FOR BIOTECHNOLOGY LABORATORIES ACCORDING TO THE DEGREE OF HAZARD

Canadian Standards Association (CSA), According to medical research

CSA ISO 10993-16-00-CAN/CSA:2000 Biological Evaluation of Medical Devices - Part 16: Toxicokinetic Study Design for Degradation Products and Leachables First Edition; ISO 10993-16: 1997