Search by property

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:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.5.3  + (7.5.3)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.6  + (7.6)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.8  + (7.8)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.9  + (7.9)
• Reference:ICH ICH E11 Guideline R1 (2017) 8  + (8)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8  + (8)
• Reference:GBR MEDDEV 2.7/3 revision 3 May-2015 8  + (8)
• Reference:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-001  + (8)
• Reference:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-002  + (8)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8 - Electronic data handling  + (8 - Electronic data handling)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8 - Introduction  + (8 - Introduction)
• Reference:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8.2-001  + (8.2)
• Reference:EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8.2-002  + (8.2)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 8.2  + (8.2)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 8.3  + (8.3)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8.3  + (8.3)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9  + (9)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.1  + (9.1)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.2  + (9.2)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.2  + (9.2.2)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.4  + (9.2.4)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.5  + (9.2.5)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 9.3  + (9.3)
• Reference:EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 A4.13  + (A4.13)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section D No. 17  + (ANNEX I Section D No. 17)

• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section D No. 19  + (ANNEX I Section D No. 19)

• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section D No.17 ; No. 22  + (ANNEX I Section D No.17 ; No. 22)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX I Section K No. 59-60  + (ANNEX I Section K No. 59-60)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX III Section 2.1  + (ANNEX III Section 2.1)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX VI Section 2.5 No. 17-22  + (ANNEX VI Section 2.5 No. 17-22)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX VI Section D No. 8  + (ANNEX VI Section D No. 8)
• Reference:GBR Directive 93/42/EEC 11-Oct-2007 ANNEX X 2.1  + (ANNEX X 2.1)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 ANNEX XV Chapter III, 6  + (ANNEX XV Chapter III, 6)
• Reference:ICH ICH E8 Guideline R1 (2021) ANNEX: TYPES OF CLINICAL STUDIES  + (ANNEX: TYPES OF CLINICAL STUDIES)
• Reference:EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022 Annex 1  + (Annex 1)
• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 2.2  + (Annex 2 2.2)
• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 2.3  + (Annex 2 2.3)
• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 2.3.2  + (Annex 2 2.3.2)
• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 2.4 - 2.5  + (Annex 2 2.4 - 2.5)
• Reference:WHO WHO - Guidance for best practices for clinical trials 2024 Annex 2 2.5  + (Annex 2 2.5)
• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 3  + (Annex 2 3)
• Reference:ICH ICH E6 Guideline - Annex 2 R3 Annex 2 Annex 2 Introduction  + (Annex 2 Introduction)
• Reference:EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 Annex 5 A5.2  + (Annex 5 A5.2)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.17  + (Annex A A.17)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.5  + (Annex A A.5)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.6.3-001  + (Annex A A.6.3)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.6.3-002  + (Annex A A.6.3)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A A.7  + (Annex A A.7)
• Reference:EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 Annex A A5.3  + (Annex A A5.3)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A - CIP  + (Annex A - CIP)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 Annex A - medical device-001  + (Annex A - medical device)