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Glossary:TAG-00001-Med-rzn

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Glossary > Medicinal product

Medicinal product
Tag-ID TAG-00001-Med-rzn
English Medicinal product / Medicine / Drug
French Médicament / Spécialité pharmaceutique
German Arzneimittel / ArzneispezialitÀt

References

 ScopeDocument partLanguageDocument
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 2 Absatz 1 – 2HM§ 2 Absatz 1 – 2DEDEU AMG - Arzneimittelgesetz 19-Jul-2023
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 2 Absatz 3HM§ 2 Absatz 3DEDEU AMG - Arzneimittelgesetz 19-Jul-2023
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 67 (6)HM§ 67 (6)DEDEU AMG - Arzneimittelgesetz 19-Jul-2023
DEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022 2.1NIS2.1DEDEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022
DEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022 2.7.7NIS2.7.7DEDEU Gemeinsame Empfehlungen - zur Anzeige von Anwendungsbeobachtungen und nichtinterventionellen Unbedenklichkeits-studien 15-Dec-2022
DEU SGB V - Sozialgesetzbuch FĂŒnftes Buch 20-Dez-1988 § 35aNIS§ 35aDEDEU SGB V - Sozialgesetzbuch FĂŒnftes Buch 20-Dez-1988
EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005 2.1HM2.1ENEU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005
GBR Medicines and Medical Devices Act 2021 21-Feb-2021 Chapter 2 Article 8GChapter 2 Article 8ENGBR Medicines and Medical Devices Act 2021 21-Feb-2021
ICH ICH E11 Guideline R1 (2017) -G-ENICH ICH E11 Guideline R1 (2017)
USA 21 CFR Part 320 09-Apr-2025 § 320.22HM§ 320.22ENUSA 21 CFR Part 320 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (g)G§ 50.3 (g)ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (j)G§ 50.3 (j)ENUSA 21 CFR Part 50 09-Apr-2025
USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 2.1.1.G2.1.1.ENUSA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - adverse reactionHMGlossary - adverse reactionENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - pharmaceutical productHMGlossary - pharmaceutical productENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995