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List of results

• Document:GBR NHS: Records Management Code of Practice 07-Aug-2023  + (NHS: Records Management Code of Practice)
• Document:USA NIH - SCORE Manual N.A.  + (NIH - SCORE Manual)
• Document:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025  + (NIH - SCORE Manual: Appendix Source Documents Requirements)
• Document:USA NIH - Glossary 27-May-2025  + (NIH - Glossary)
• Document:GBR NIHR - National Institute for Health and Care Research 28-Jan-2025  + (NIHR - National Institute for Health and Care Research)
• Document:GBR National Health Service Act 2006 02-Dec-2019  + (National Health Service Act 2006)
• Document:INT Nuremberg Code 1947  + (Nuremberg Code)
• Document:AUT Question - BASG 11-Feb-2025  + (Question - BASG)
• Document:USA Recognized Consensus Standards N.A.  + (Recognized Consensus Standards)
• Document:USA Recognized Consensus Standards - ISO 14155 21-Dec-2020  + (Recognized Consensus Standards - ISO 14155)
• Document:EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017  + (Recommendations of the expert group - Risk proportionate approaches in clinical trials)
• Document:EU ; GBR Regulation (EC) No 1223/2009 - Cosmetic Products 01-Dec-2023  + (Regulation (EC) No 1223/2009 - Cosmetic Products)
• Document:EU ; GBR Regulation (EC) No 178/2002 - Food Safety 01-Jul-2022  + (Regulation (EC) No 178/2002 - Food Safety)
• Document:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22  + (Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use)
• Document:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016  + (Regulation (EU) 2016/679 (GDPR))
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble  + (Regulation (EU) 2017/745 - Medical Device Regulation)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023  + (Regulation (EU) 2017/745 - Medical Device Regulation)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble  + (Regulation (EU) 2017/746 - in vitro diagnostic medical devices)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023  + (Regulation (EU) 2017/746 - in vitro diagnostic medical devices)
• Document:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022  + (Regulation (EU) 536/2014 - clinical trials)
• Document:EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble  + (Regulation (EU) 536/2014 - clinical trials)
• Document:EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014  + (Regulation (EU) 910/2014 - electronic identification)
• Document:EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12  + (Regulation (EU) No 520/2012 - performance of pharmacovigilance activities)
• Document:DEU Richtlinie zur Bewertung der Qualifikation von Prüfern, Hauptprüfern, Leitern und ärztlichen Mitgliedern von Prüfungsteams durch Ethik-Kommissionen von Arbeitskreis Medizinischer Ethik-Kommissionen in der Bundesrepublik Deutschland e. V. und  + (Richtlinie zur Bewertung der Qualifikation … Richtlinie zur Bewertung der Qualifikation von Prüfern, Hauptprüfern, Leitern und ärztlichen Mitgliedern von Prüfungsteams durch Ethik-Kommissionen von Arbeitskreis Medizinischer Ethik-Kommissionen in der Bundesrepublik Deutschland e. V. und Bundesärztekammerik Deutschland e. V. und Bundesärztekammer)

• Document:DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988  + (SGB V - Sozialgesetzbuch Fünftes Buch)

• Document:FRA SI RIPH 2G - Website 16-May-2025  + (SI RIPH 2G - Website)
• Document:SMW Test  + (SMW Test Document)
• Document:N.A. SPIRIT 2013 - Chan et al. 2013  + (SPIRIT 2013 - Chan et al.)
• Document:FRA SURV VIG DOC118 V01 REC-Avis aux promoteurs -Partie V 16-May-2025  + (SURV_VIG_DOC118 V01 REC-Avis aux promoteurs -Partie V)
• Document:DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022  + (StrlSchG - Strahlenschutzgesetz)
• Document:DEU StrlSchV - Strahlenschutzverordnung 08-Oct-2021  + (StrlSchV - Strahlenschutzverordnung)
• Document:DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024  + (TAMG - Tierarzneimittelgesetz)
• Document:GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019  + (The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019)
• Document:GBR The Human Medicines Regulations 2012 01-Jan-2025  + (The Human Medicines Regulations 2012)
• Document:GBR The Medical Devices Regulations 2002 11-Feb-2021  + (The Medical Devices Regulations 2002)
• Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004  + (The Medicines for Human Use (Clinical Trials) Regulations 2004)
• Document:N.A. Transcelerate GCP mutual recognition programm FAQ 21-May-2025  + (Transcelerate GCP mutual recognition programm FAQ)
• Document:USA U.S. Code Title 21 30-Sep-2023  + (U.S. Code Title 21)
• Document:GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020  + (UK GDPR - United Kingdom General Data Protection Regulation)
• Document:USA WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591 46114  + (WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591)
• Document:WHO WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS Forty-fifth report  + (WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS)
• Document:WHO WHO - Guidance for best practices for clinical trials 2024  + (WHO - Guidance for best practices for clinical trials)
• Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995  + (WHO - Guidelines for GCP for trials on pharmaceutical products*)
• Document:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005  + (WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP))
• Document:WHO WHO - ICD 11  + (WHO - ICD)
• Document:WHO WHO Good Practices for Clinical Trial Design and Implementation 04-May-2026  + (WHO Good Practices for Clinical Trial Design and Implementation)
• Document:WHO World Health Organization -  + (World Health Organization)
• Document:AUT Ärztegesetz 08-Mar-2023  + (Ärztegesetz)