Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
Our Services
Your Trusted Partner in Global Regulatory Excellence
Empowering life sciences organizations with regulatory clarity, operational excellence, and a commitment to patient safety.
Regulatory Affairs Services
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, audits/inspection readiness, and PSMF governance.
Qualified Person (QP) Services (GMP)
Our QP services ensure full compliance with EU and UK GMP requirements safeguarding product quality, integrity, and patient safety from batch release to market distribution.
Gap Analysis & Inspection Readiness
At GLORAMP, 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 of your product 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
At GLORAMP, we help medical device and IVD manufacturers navigate the complex landscape of EU MDR, IVDR, UKCA, and FDA regulations — from strategy to certification.
GxP, Quality & Compliance
At GLORAMP, we provide comprehensive QA and QC services that strengthen your quality systems, ensure regulatory compliance, and maintain product integrity throughout the lifecycle.
eTMF Support
GLORAMP Pharma Consulting Ltd provides comprehensive 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.
Book a free call
Let’s talk! Book a free 30-minute call with a senior team member to explore how we can support your goals.