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Document: Response to Paediatric Committee request for supplementary information and modification of proposed PIP (RSI) - Re-submission following clock-stop-2025/7/28
2025-07-29查看详情 > -
Document: Key elements form: Applicant’s proposal for a paediatric-investigation-plan opinion-2025/7/28
2025-07-29查看详情 > -
Document: Template for scientific document for paediatric investigation plan or product-specific waiver-2025/7/28
2025-07-29查看详情 > -
Document: Procedural advice on paediatric applications-2025/7/28
2025-07-29查看详情 > -
Page: COVID-19 vaccines: key facts-2025/7/28
2025-07-29查看详情 > -
Document: Substances considered as not falling within the scope of Regulation (EC) No. 470/2009, with regard to residues of veterinary medicinal products in foodstuffs of animal origin-2025/7/25
2025-07-27查看详情 > -
Document: IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants-2025/7/25
2025-07-27查看详情 > -
Page: ICH Guideline M13B on bioequivalence for immediate-release solid oral dosage forms - additional strengths biowaiver - Scientific guideline-2025/7/25
2025-07-27查看详情 > -
Document: Overview of comments received on ICH M13B guideline on bioequivalence for immediate-release solid oral dosage forms - additional strengths biowaiver (EMA/CHMP/ICH/85092/2025)-2025/7/25
2025-07-27查看详情 > -
Document: HMPC meeting report on European Union herbal monographs, guidelines and other activities - 07-09 July 2025-2025/7/25
2025-07-27查看详情 >