Search by property
From GxPlex
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:GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019 - +
- Reference:USA 21 CFR Part 11 09-Apr-2025 § 11.3 (b) (5) ; (b) (7) ; (b) (8) +
- Reference:USA 21 CFR Part 11 09-Apr-2025 § 11.50 +
- Reference:USA 21 CFR Part 11 09-Apr-2025 § 11.70 +
- Reference:USA 21 CFR Part 11 09-Apr-2025 § 11.100 +
- Reference:USA 21 CFR Part 11 09-Apr-2025 § 11.200 +
- Reference:USA 21 CFR Part 11 09-Apr-2025 § 11.300 +
- Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Case Report Form (CRF) +
- Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Data Acquisition Tool (DAT) +
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.2.1 +
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 4.2.3 - 4.2.4 +
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - case -report form (CRF) +
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 6.6 +
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 56 +
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 57 +
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Paragraph 3 – 4-001 +
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter III Paragraph 3 +
- Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 3 – 4-001 +
- Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 3-001 +
- Reference:DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.8 +
- Reference:USA 21 CFR Part 314 09-Apr-2025 § 314.50 +
- Reference:ICH ICH E6 Guideline R3 (2025) III. Annex 1 3.11.4 3.11.4.3 - 3.11.4.6 +
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - monitor +
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - verification (validation) of data +
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-001 +
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 6 +
- Reference:ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9.2.4 +
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 48 +
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Pragraph 2 +
- Reference:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter III Section 4 +
