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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• 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)