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EDQM Database
What do you need to know about the database?
The European Directorate for the Quality of Medicines & HealthCare (EDQM) maintains several databases to regulate the quality and safety of medicines and healthcare products in Europe. These databases provide valuable information for pharmaceutical professionals, regulatory bodies, and researchers.
The European Pharmacopoeia (Ph. Eur.) database is a key resource containing monographs on active pharmaceutical ingredients, excipients, and finished medicinal products. It ensures that medicines meet strict quality standards for manufacturing, testing, and quality control.
Additionally, the European Reference Materials (ERM) database offers access to certified reference materials essential for validating laboratory testing and ensuring consistency in pharmaceutical quality control.
The EDQM also manages a database on substances of human origin, providing standards for blood, tissues, organs, and cells used in transplantation and transfusion.
These databases play a crucial role in ensuring medicine safety, promoting transparency, and supporting regulatory compliance across Europe.
Database Administrator
Managed by: Council of Europe
What data are included in the database?
- European Pharmacopoeia (Ph. Eur.): Quality standards and monographs for active ingredients, excipients, and finished medicinal products.
- European Reference Materials (ERM): Certified reference materials for laboratory testing and quality control in the pharmaceutical industry.
- Substances of Human Origin: Regulatory guidelines for blood, tissues, and organs used in transplantation and transfusion.
- Counterfeit Medicines: Information on detecting and preventing counterfeit medicines to ensure public safety.
- Regulatory Guidelines: Compliance documents and harmonization standards for pharmaceutical manufacturing and drug safety.
How to search the database?
- Access the Database: Visit the EDQM website and select the desired database.
- Search by Keywords: Use the search bar to find specific pharmaceutical monographs, reference materials, or regulatory guidelines.
- Filter Results: Apply filters by substance type, regulatory category, or quality standards.
- Download Data: Retrieve documents, guidelines, and reference materials in various formats for further analysis.
Related Resources
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