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Property:RefTags

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Raw TAG-ID list for this reference (used for glossary queries).

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Showing 20 pages using this property.
U
USA 21 CFR Part 312 09-Apr-2025 § 312.32 - Unexpected adverse event +
TAG-00331-Une-irk ++ TAG-00003-Adv-cht ++ TAG-00045-Adv-hte ++ TAG-00244-Def-ini ++ TAG-00034-Inv-Bro ++ TAG-00320-Foo-eri  +
D
DEU DGEPi - GEP Guter Epidemiologischer Praxis Sep-2018 Leitlinie 6 6.4 +
TAG-00334-Tra-ngP ++ TAG-00144-Qua-gew ++ TAG-00010-Non-Stu  +
W
WHO WHO - Guidance for best practices for clinical trials 2024 3.2.4 +
TAG-00334-Tra-ngP ++ TAG-00335-Ret-uff ++ TAG-00340-Req-nfo ++ TAG-00338-Met-odi  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - 1.5 Regulatory requirements +
TAG-00340-Req-nfo ++ TAG-00061-Cli-rtr ++ TAG-00017-Spo-die ++ TAG-00246-Inv-hte ++ TAG-00341-Res-ben  +
E
EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 4.2 +
TAG-00341-Res-ben ++ TAG-00127-Com-meC ++ TAG-00017-Spo-die ++ TAG-00246-Inv-hte ++ TAG-00306-Dat-nDa  +
I
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2.2 +
TAG-00342-Sit-der ++ TAG-00083-Enr-enr ++ TAG-00018-Inv-die ++ TAG-00017-Spo-die  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.7 +
TAG-00342-Sit-der ++ TAG-00135-Inv-ntr ++ TAG-00329-Saf-lne ++ TAG-00340-Req-nfo  +
E
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 56 +
TAG-00343-Doc-ten ++ TAG-00095-Sto-ung ++ TAG-00129-Dat-ali ++ TAG-00063-Dat-per ++ TAG-00017-Spo-die  +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8 +
TAG-00343-Doc-ten ++ TAG-00122-Aud-Aud ++ TAG-00129-Dat-ali ++ TAG-00306-Dat-nDa  +
E
EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011 4 +
TAG-00343-Doc-ten ++ TAG-00129-Dat-ali  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Paragraph 3 – 4-001 +
TAG-00343-Doc-ten ++ TAG-00129-Dat-ali ++ TAG-00201-Cli-eSt ++ TAG-00017-Spo-die ++ TAG-00063-Dat-per  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 3 – 4-001 +
TAG-00343-Doc-ten ++ TAG-00129-Dat-ali ++ TAG-00231-Per-ung ++ TAG-00017-Spo-die ++ TAG-00063-Dat-per  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter II Section 1.7 +
TAG-00343-Doc-ten ++ TAG-00201-Cli-eSt ++ TAG-00202-Inv-Pro ++ TAG-00017-Spo-die  +
U
USA 21 CFR Part 812 09-Apr-2025 § 812.140 (b) (5) +
TAG-00343-Doc-ten ++ TAG-00208-Dev-ers ++ TAG-00017-Spo-die ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri  +
E
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter I Section 1.8 +
TAG-00343-Doc-ten ++ TAG-00231-Per-ung ++ TAG-00235-Int-stu ++ TAG-00176-Ris-erh  +
U
USA 21 CFR Part 812 09-Apr-2025 Subpart G +
TAG-00343-Doc-ten ++ TAG-00272-Ret-enA ++ TAG-00271-Ret-Arc ++ TAG-00155-Med-Med ++ TAG-00320-Foo-eri  +
D
DEU BGB - Bürgerliches Gesetzbuch 22-Dec-2023 § 630 +
TAG-00343-Doc-ten ++ TAG-00341-Res-ben  +
G
GBR MHRA GCP Inspection Dossier template V7.0 - +
TAG-00344-Art-ngK ++ TAG-00044-Ins-ion ++ TAG-00324-Med-Age ++ TAG-00043-Goo-tek  +
E
EU European Medicines Agency’s Data Protection: Notice For Microsoft (MS) Copilot 365 - EMA pilot phase ; EMA/216030/2025 45838 - +
TAG-00344-Art-ngK ++ TAG-00058-Eur-zne ++ TAG-00176-Ris-erh  +
U
USA WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591 46114 - +
TAG-00344-Art-ngK ++ TAG-00117-Ins-sfe ++ TAG-00035-Man-odu ++ TAG-00320-Foo-eri ++ TAG-00328-Com-egu  +
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