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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

• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 4  + (Article 80 Paragraph 4)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 80 Paragraph 5 – 6  + (Article 80 Paragraph 5 – 6)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 82  + (Article 82)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 82 Paragraph 3 – 5  + (Article 82 Paragraph 3 – 5)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 87 Paragraph 1 – 2  + (Article 87 Paragraph 1 – 2)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 87 Paragraph 3 – 5  + (Article 87 Paragraph 3 – 5)
• Reference:FRA Constitution du 4 octobre 1958 10-Mar-2024 Article 89  + (Article 89)
• Reference:GBR Directive 93/42/EEC 11-Oct-2007 Article 9  + (Article 9)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 9  + (Article 9)
• Reference:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016 Article 9 Paragraph 1  + (Article 9 Paragraph 1)
• Reference:GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020 Article 9 Paragraph 1  + (Article 9 Paragraph 1)
• Reference:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016 Article 9 Paragraph 2  + (Article 9 Paragraph 2)
• Reference:GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020 Article 9 Paragraph 2  + (Article 9 Paragraph 2)
• Reference:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 Article R1121-3-1  + (Article R1121-3-1)
• Reference:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 Article R1123-20  + (Article R1123-20)
• Reference:FRA Code de la Santé Publique - Partie Réglementaire - 1ere partie, Livre 1er, Titre II 16-May-2025 Article R1123-20-1  + (Article R1123-20-1)
• Reference:GBR Medicines and Medical Devices Act 2021 21-Feb-2021 Chapter 2 Article 8  + (Chapter 2 Article 8)
• Reference:INT Nuremberg Code 1947 Code  + (Code)
• Reference:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 D Investigator/Institution  + (D Investigator/Institution)
• Reference:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 D What needs to be reported  + (D What needs to be reported)
• Reference:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 D When should the notification be made  + (D When should the notification be made)
• Reference:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 D Who should notify  + (D Who should notify)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Adverse Drug Reaction (ADR)  + (GLOSSARY - Adverse Drug Reaction (ADR))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Adverse Event (AE)  + (GLOSSARY - Adverse Event (AE))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Agreement  + (GLOSSARY - Agreement)

• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Audit  + (GLOSSARY - Audit)

• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Blinding/Masking  + (GLOSSARY - Blinding/Masking)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Case Report Form (CRF)  + (GLOSSARY - Case Report Form (CRF))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Certified Copy  + (GLOSSARY - Certified Copy)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Clinical Trial  + (GLOSSARY - Clinical Trial)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Clinical Trial/Study Report (CSR)  + (GLOSSARY - Clinical Trial/Study Report (CSR))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Comparator  + (GLOSSARY - Comparator)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Compliance (in relation to trials)  + (GLOSSARY - Compliance (in relation to trials))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Computerised Systems Validation  + (GLOSSARY - Computerised Systems Validation)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Contract Research Organisation (CRO)  + (GLOSSARY - Contract Research Organisation (CRO))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Data Acquisition Tool (DAT)  + (GLOSSARY - Data Acquisition Tool (DAT))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Data Integrity  + (GLOSSARY - Data Integrity)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Independent Data Monitoring Committee (IDMC)  + (GLOSSARY - Independent Data Monitoring Committee (IDMC))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Informed Consent  + (GLOSSARY - Informed Consent)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Inspection  + (GLOSSARY - Inspection)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Institutional Review Board (IRB)/Independent Ethics Committee (IEC)  + (GLOSSARY - Institutional Review Board (IRB)/Independent Ethics Committee (IEC))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Interim Clinical Trial/Study Report  + (GLOSSARY - Interim Clinical Trial/Study Report)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigational Product  + (GLOSSARY - Investigational Product)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator  + (GLOSSARY - Investigator)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator’s Brochure (IB)  + (GLOSSARY - Investigator’s Brochure (IB))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Metadata  + (GLOSSARY - Metadata)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Protocol Amendment  + (GLOSSARY - Protocol Amendment)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Randomisation  + (GLOSSARY - Randomisation)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Regulatory Authorities  + (GLOSSARY - Regulatory Authorities)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Serious Adverse Event (SAE)  + (GLOSSARY - Serious Adverse Event (SAE))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Service Provider  + (GLOSSARY - Service Provider)