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Page: Good agricultural and collection practice for starting materials of herbal origin - Scientific guideline-2025/8/12
2025-08-13查看详情 > -
Document: Combined VeDDRA list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products-2025/8/12
2025-08-13查看详情 > -
Page: Pre-authorisation guidance-2025/8/12
2025-08-13查看详情 > -
Document: European Medicines Agency Write PMS API implementation Guide (zip)-2025/8/11
2025-08-12查看详情 > -
Document: European Medicines Agency Write PMS API implementation Guide-2025/8/11
2025-08-12查看详情 > -
Document: Product Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 2 - track changes-2025/8/8
2025-08-10查看详情 > -
Document: Product Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 2-2025/8/8
2025-08-10查看详情 > -
Document: Paediatric investigation plan (PIP) - Key elements form-2025/8/8
2025-08-10查看详情 > -
Document: Procedural advice on paediatric applications-2025/8/8
2025-08-10查看详情 > -
Page: Paediatric medicines: applications and procedures-2025/8/8
2025-08-10查看详情 >