Pages that link to "Glossary:TAG-00135-Inv-ntr"

The following pages link to Glossary:TAG-00135-Inv-ntr:

Displaying 26 items.

• Glossary (← links)
• Reference:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 Overview of the Clinical Research Process (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 (1) (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) Appendix C C.2.3 (← links)
• Reference:EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018 3 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 1.4 (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 investigator (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 49 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.7 (← links)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 10.3 (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 50 (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Schedule 3 Part 1 1. (← links)
• Reference:GBR GUIDANCE FOR THE NOTIFICATION OF SERIOUS BREACHES OF GCP OR THE TRIAL PROTOCOL 08-Jul-2020 Appendix I (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.12.11 – 2.12.14 (← links)
• Reference:USA FDA Guidance for Industry - Computerized Systems Used in Clinical Investigations May-2007 IV (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 6 (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 6.2 (← links)
• Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 15 (← links)
• Reference:DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 41 (← links)
• Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.11 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Inspection (← links)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 11.2 (← links)
• Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Pragraph 5 (← links)
• Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 5 (← links)
• Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 32 (← links)
• Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.11.4.5.2 (← links)