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Latest Regulatory & Industry Updates — November 2025

Insights curated by GLORAMP Pharma Consulting LtdStay informed with the most recent developments from leading…

  • athershathiByathershathi
  • OnNovember 14, 2025
  • BlogNews

Supply Chain & Sustainability Pressures

European authorities are tightening requirements around medicine availability and environmental sustainability. What This Means for…

  • athershathiByathershathi
  • OnNovember 10, 2025
  • News

🇪🇺 European Medicines Agency (EMA) Meeting Highlights from the CHMP 13–16 October 2025

The EMA’s Committee for Medicinal Products for Human Use (CHMP) reviewed several marketing authorisations and…

  • athershathiByathershathi
  • OnAugust 18, 2020
  • NewsUseful

🇬🇧 Medicines and Healthcare Products Regulatory Agency (MHRA) GMP & GDP Certificate Updates 2025

The MHRA Inspectorate released an update reminding manufacturers and wholesalers about the renewal and recognition…

  • 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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  • QP Batch release
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  • eTMF Support
  • Compliance Audits.

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