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Gloramp
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🇺🇸 U.S. Food and Drug Administration (FDA) Framework for AI Models in Regulatory Submissions

The FDA published a draft framework for assessing Artificial Intelligence and Machine Learning models used…

  • athershathiByathershathi
  • OnAugust 18, 2020
  • News

🧾 CMDh — Coordination Group for Mutual Recognition and Decentralised Procedures (Human)

CMDh issued updated guidance covering the management of variations, national requirements, and harmonisation between mutual-recognition…

  • athershathiByathershathi
  • OnAugust 18, 2020
  • News

European Directorate for the Quality of Medicines & HealthCare (EDQM) EDQM 2024 Annual Report — Commitment to Public Health

The EDQM’s annual report highlights achievements in reference standards, laboratory accreditation, and quality-management expansion across…

  • athershathiByathershathi
  • OnAugust 18, 2020
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At GLORAMP Pharma Consulting, we monitor these developments daily to help our clients stay ahead of change and fully compliant. For guidance tailored to your organisation — from regulatory strategy to PV and QP support — contact us at

📧 info@gloramppharma.co.uk

About Us

We partner with pharmaceutical, biopharma and device manufacturers to deliver regulatory, pharmacovigilance, quality solutions and end-to-end compliance worldwide— with agility, scientific depth and global readiness.

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  • 📧 info@gloramppharma.co.uk

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  • Phone: +44 1296 790 435
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Core Services:

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  • Pharmacovigilance(QPPV)
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  • QP Batch release
  • Wholesale Dealer Authorisation (WDA)
  • eTMF Support
  • Compliance Audits.

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Based in the UK and Ireland, supporting clients worldwide

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