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Gloramp
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    • Regulatory Affairs Services​
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    • Gap Analysis & Inspection Readiness
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Gloramp
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Digital & AI Integration in Compliance

Digital technologies and AI are transforming pharmacovigilance, clinical documentation (eTMF), and regulatory operations. What This…

  • athershathiByathershathi
  • OnDecember 10, 2025
  • News

Evolving GMP/GDP and Quality Expectations

Upcoming GMP revisions emphasise digital traceability, data integrity, and supply-chain accountability. What This Means for…

  • athershathiByathershathi
  • OnDecember 10, 2025
  • News

🇬🇧 Post-Brexit UK Regulatory Framework

The UK continues to refine its own regulatory pathways for manufacturers and wholesalers. This includes…

  • athershathiByathershathi
  • OnDecember 10, 2025
  • News

Major Industry Changes Affecting Pharmaceutical Companies 🇪🇺 EU Pharma Package Reform 2025

The European Commission is reshaping market-exclusivity periods, supply-chain duties, and orphan-drug incentives through the upcoming…

  • athershathiByathershathi
  • OnDecember 10, 2025
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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.

Email

  • 📧 info@gloramppharma.co.uk

Contact Us

  • Phone: +44 1296 790 435
  • Mobile: +44 7917353129

Core Services:

  • Regulatory Affairs
  • Pharmacovigilance(QPPV)
  • Manufacturer/Importer (MIA)
  • QP Batch release
  • Wholesale Dealer Authorisation (WDA)
  • eTMF Support
  • Compliance Audits.

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Global Presence:

Based in the UK and Ireland, supporting clients worldwide

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