Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
Our story
Your Trusted Partner in Global Regulatory Excellence
Empowering life sciences organizations with regulatory clarity, operational excellence, and a commitment to patient safety.
Story video
Company Values
GLORAMP was formed in 2014 in the UK/EU with a singular focus to provide Regulatory services,Pharmacovigilance services and Ad hoc services e.g., Act as UK/EU ‘Virtual’ MAH support,Manufacturers/Importers (MIA) Holder support to pharmaceutical companies. Our technology platformis 21 CFR Part 11 compliant and is able to support hosted access to validated Regulatory,Pharmacovigilance database and Quality system. To our clients, regardless of global location, we are ableto provide single points of contact and control to fully meet customer service needs.
GLORAMP takes pride in providing very high-quality solutions to our customers and fully understand theGlobal compliance requirements and encompass these at every stage in GLORAMP’s processes andprocedures. Our fee structure is simple and the GLORAMP team will provide the highest level ofprofessional service with international expertise along with a cost-effective and efficient environment.
We know compliance matters!
GLORAMP brings senior regulatory strategists, QPPVs, QPs, quality leaders, and publishing specialiststogether under one roof to support the global pharmaceutical industry.
Our Mission
To help pharmaceutical and biotech companies bring safe, effective products to market whilemaintaining the highest standards of compliance and patient safety.
Our Team
Led by industry professionals with decades of experience in regulatory and pharmacovigilance, ourconsultants are trusted advisors to companies across Europe and beyond. Our team has run global PVsystems, performed GMP/GDP audits, certified batches, and delivered thousands of eCTD submissionsfor SMEs and top pharma companies via validated, audit-ready workflows.
Patient safety first
We prioritize patient safety above all else ensuring compliance and vigilance across Pharmacovigilance (PV), Quality Management Systems (QMS), and Post-Market Surveillance (PMS) activities.
Regulatory Clarity
We bring end-to-end regulatory clarity — from strategy to execution — across the UK, EU, and key global markets, enabling faster, compliant market access.
Operational Excellence
We drive operational excellence by aligning all GxP processes with EudraLex and MHRA expectations, ensuring quality, consistency, and audit readiness at every stage.
Why Choose GLORAMP?
Trusted regulatory experts delivering flexible, end-to-end solutions — ensuring compliance, quality, and patient safety across global markets.
Proven Regulatory Expertise
With extensive experience across EU, UK, and global regulatory frameworks, we ensure your products meet every compliance requirement with confidence.
Tailored, Flexible Solutions
We design adaptable strategies that align with your business goals — whether you’re a start-up or a global enterprise.
Comprehensive Lifecycle Support
From early development to post-marketing surveillance, we provide seamless, end-to-end regulatory and quality support at every stage.
Unwavering Commitment to Quality & Safety
Our work is guided by a steadfast focus on quality, compliance, and patient safety — the foundation of everything we do.
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.