Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
Your Partner in Global Pharma Compliance Excellence
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.
About GLORAMP Pharma Consulting Ltd
GLORAMP Pharma Consulting Ltd provides expert Regulatory Affairs, Pharmacovigilance (QPPV), Quality Assurance & Control, and Qualified Person (QP) services for pharmaceutical, biopharma, and medical device/IVD manufacturers. Our offerings include Marketing Authorisation Holder, Manufacturers/Importer Authorisation/Batch Release, Medical Information, Wholesale Dealers Authorisation, Electronic Common Technical Documents/Non- electronic Common Technical Documents publishing, Artwork & Labeling, Package Information Leaflet User Testing, and Compliance Gap Analysis.
We help clients achieve and maintain UK, EU, and global regulatory compliance efficiently and right-first-time, offering Virtual Marketing Authorisation Holder, Manufacturers/Importer Authorisation Holder support, and access to our 21 CFR Part 11–compliant technology platform.
End-to-end support
End-to-end support from R&D to post-market, covering strategy, submissions, vigilance, and compliant distribution.
Hands-on UK/EU and RoW expertise
Fully aligned with MHRA, EMA, EU, and RoW authorities, following all relevant regulations and guidelines.
Flexible engagement
Flexible engagement — project-based, fractional QPPV/QP, or fully managed services.
What we do
GLORAMP Pharma Consulting simplifies global regulatory and quality compliance for life-science innovators.
We deliver practical, inspection-ready solutions that keep your products safe, effective, and compliant worldwide.
Regulatory Affairs
we deliver end-to-end Regulatory Affairs support — from early development to post-approval — ensuring compliance, quality, and faster market access across the UK, EU, and global regions.
Pharmacovigilance & QPPV
Turnkey PV systems (clinical → post-marketing) including case processing, signal management, PSUR/PBRER, RMPs, inspection readiness, and PSMF governance.
Qualified Person (QP)
Our QP services ensure full compliance with EU and UK Good Manufacturing Practice (GMP) requirements — safeguarding product quality, integrity, and patient safety from batch release.
GxP, Quality & Compliance
we provide comprehensive QA and QC services that strengthen your quality systems, ensure regulatory compliance, and maintain product integrity throughout the lifecycle.
eCTD Publishing & Regulatory Operations
we deliver high-quality, compliant, and efficient eCTD publishing and regulatory operations that support successful global submissions and lifecycle management.
Medical Devices & IVD Services (MDR/IVDR)
we help medical device and IVD manufacturers navigate the complex landscape of EU MDR, IVDR, UKCA, and FDA regulations — from strategy to certification.
Gap Analysis & Inspection Readiness
We help organizations proactively identify compliance gaps, mitigate regulatory risks, and achieve full inspection readiness across GxP functions.
Artwork, Labeling & Packaging Operations
We provide end-to-end regulated artwork and labeling management services ensuring accuracy, compliance, and efficiency across every stage.
eTMF Support
eTMF (electronic Trial Master File) support to ensure your clinical documentation remains compliant, inspection-ready, and aligned with ICH E6 (GCP) and EMA/FDA regulatory expectations
Some Insights
We’re proud to support clients across pharma, biotech, and medical device sectors helping them stay compliant, inspection-ready, and globally competitive.
What peoples say about us
Discover how we’ve helped others achieve their goals.
“GLORAMP guided us through complex regulatory submissions with clarity and precision — their support was invaluable during inspection.”
Patricia Muller
Regulatory Affairs Manager, UK Biotech Company
“Their pharmacovigilance expertise helped us strengthen our global safety system — professional, responsive, and always audit-ready.”
Michael Clark
Director, Global PV Operations, EU Pharma
“Exceptional quality support — from gap analysis to QMS implementation, they delivered practical solutions tailored to our needs.”
Kent Milestone
QA Lead, Medical Device Manufacturer
Achievements
Successfully supported regulatory submissions and PV setups for clients in over 15 countries. Delivered multiple MHRA and EMA inspection-readiness projects with 100% compliance outcomes. Recognised for expertise in eTMF implementation, QMS audits, and regulatory strategy across pharma and device sectors.
The life-sciences landscape is evolving fast and so are we. At GLORAMP, we turn complex global regulatory and quality requirements into clear, actionable pathways that keep your business compliant, efficient, and future-ready