Richtlijnen Kennisbank
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Beschikbare richtlijnen
74 resultaten
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Commission Staff Working Document SWD(2025) 244 on the use of titanium dioxide in medicinal products
Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/commission-staff-working-document-use-titanium-dioxide-medicinal-products-2025-08-06_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/document-summarising-evidence-supporting-legislative-proposal-strengthening-availability-supply-and-2025-09-03_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/new-and-updated-documents-eudralex-volume-10-clinical-trials-guidelines-2025-10-30_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/new-and-updated-documents-eudralex-volume-10-clinical-trials-guidelines-2025-10-30_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/new-and-updated-documents-eudralex-volume-10-clinical-trials-guidelines-2025-10-30_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/new-and-updated-documents-eudralex-volume-10-clinical-trials-guidelines-2025-10-30_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/2024-annual-report-paediatric-medicines-regulation-2025-12-18_en).
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Imported from European Commission — EudraLex (https://health.ec.europa.eu/latest-updates/questions-and-answers-version-22-safety-features-medicinal-products-human-use-2026-07-10_en).
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Imported from U.S. Food and Drug Administration (https://www.fda.gov/drugs/guidances-drugs/product-specific-guidances-generic-drug-development).
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Imported from U.S. Food and Drug Administration (http://www.fda.gov/vaccines-blood-biologics/guidance-compliance-regulatory-information-biologics/biologics-procedures-sopps).
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