The Future of Medicinal Product Registration: What You Need to Know ????
Stay Ahead in Pharma: Navigating the EDA’s Guidelines?????
Welcome to the first edition of our Regulatory Insights newsletter! ?? In this issue,
The EDA has just released the latest Guidelines on Reliance Practices During Registration of Medicinal Products. This comprehensive document aligns with WHO guidelines and aims to streamline regulatory activities, ensuring efficient and effective registration processes. ????
?? ?Key Highlights:
? Enhanced Collaboration: Leveraging global expertise to avoid duplication and focus on value-added regulatory activities.
? Quality Assurance: Rigorous evaluation of product quality, bioavailability, stability, and clinical data.
? Public Health Focus: Prioritizing medicinal products for unmet medical needs and public health emergencies.
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Dive into the full guidelines to stay ahead in the pharmaceutical industry and ensure compliance with the latest standards. ????
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Check reference for more details
https://edaegypt.gov.eg/media/2rydqaxz/guide-line-reliance-practices-during-registration-of-medicinal- products.pdf
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