Most linked-to pages

Showing below up to 50 results in range #1,351 to #1,400.

1351. Glossary:TAG-00198-Not-Not (5 links)
1352. Glossary:TAG-00256-GCP-CPZ (5 links)
1353. Glossary:TAG-00263-EUD-izi (5 links)
1354. Glossary:TAG-00275-Lay-ndl (5 links)
1355. Glossary:TAG-00281-Und-sse (5 links)
1356. Glossary:TAG-00284-Pos-ngn (5 links)
1357. Glossary:TAG-00292-Eme-ent (5 links)
1358. Glossary:TAG-00301-Cli-eII (5 links)
1359. Glossary:TAG-00304-Pri-tSt (5 links)
1360. Glossary:TAG-00337-His-tor (5 links)
1361. Document:AUT FAQ - COVID-19 Studien 15-Mar-2021 (4 links)
1362. Document:AUT MPG – Medizinproduktegesetz 26-May-2022 (4 links)
1363. Document:AUT Question - BASG 11-Feb-2025 (4 links)
1364. Document:DEU AMWHV – Arzneimittel- und Wirkstoffherstellungs-verordnung 09-Aug-2019 (4 links)
1365. Document:DEU Deutsches Ärzteblatt 45849 (4 links)
1366. Document:DEU MPAMIV - Medizinprodukte-Anwendermelde- und Informationsverordnung 21-Apr-2021 (4 links)
1367. Document:DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988 (4 links)
1368. Document:DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022 (4 links)
1369. Document:EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005 (4 links)
1370. Document:EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011 (4 links)
1371. Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble (4 links)
1372. Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble (4 links)
1373. Document:EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble (4 links)
1374. Document:EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12 (4 links)
1375. Document:FRA SI RIPH 2G - Website 16-May-2025 (4 links)
1376. Document:GBR Data Protection Act 2018 06-Jun-2022 (4 links)
1377. Document:GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015 (4 links)
1378. Document:GBR MHRA GCP Inspection Dossier template V7.0 (4 links)
1379. Document:GBR NHS: Records Management Code of Practice 07-Aug-2023 (4 links)
1380. Document:GBR The Human Medicines Regulations 2012 01-Jan-2025 (4 links)
1381. Document:ICH ICH E19 Guideline 2022 (4 links)
1382. Document:ICH ICH E21 Concept paper 2023 (4 links)
1383. Document:ICH ICH E2F Guideline 2010 (4 links)
1384. Document:INT ISPE - GPP Revision 3 (2015) (4 links)
1385. Document:INT Nuremberg Code 1947 (4 links)
1386. Document:N.A. (STROBE)statement: guidelines for reporting observational studies Apr-2008 (4 links)
1387. Document:N.A. Minimum Criteria for ICH E6 (R3) GCP Investigator Site Personnel Training V3.0 (4 links)
1388. Document:USA 21 CFR Part 320 09-Apr-2025 (4 links)
1389. Document:USA 21 CFR Part 809 06-May-2024 (4 links)
1390. Document:USA Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff 21-Feb-2018 (4 links)
1391. Document:USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 (4 links)
1392. Document:USA FDA Guidance for Industry - Computerized Systems Used in Clinical Trials 13-Apr-2015 (4 links)
1393. Document:USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998 (4 links)
1394. Document:USA FDA Information - Observations and citations 20-Mar-2024 (4 links)
1395. Document:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 (4 links)
1396. Document:WHO WHO Good Practices for Clinical Trial Design and Implementation 04-May-2026 (4 links)
1397. Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40a (4 links)
1398. Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b-001 (4 links)
1399. Reference:DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 4 Absatz 24 (4 links)
1400. Reference:DEU BGB - Bürgerliches Gesetzbuch 22-Dec-2023 § 630 (4 links)