Accelerating Pharma
Access Across Borders
Trusted global partner for Pharma Distribution, Licensing, and Regulatory Navigation.
Why 
Who We Are
VigiRA Med Ltd is a UK-based pharmaceutical consultancy founded by Santhoshkumar Veerabomma, offering end-to-end support in Pharmacovigilance (PV), Regulatory Affairs (RA), Quality Assurance (QA), and Responsible Person (RP) services. With deep expertise in the UK and EU regulatory landscape, VigiRA Med bridges the gap between compliance and commercial success for Marketing Authorisation Holders (MAHs), distributors, and healthcare businesses.
Our mission is to deliver tailored, compliant, and cost-effective solutions that allow our clients to focus on growth while we ensure their medicines meet the highest standards of safety and regulatory oversight.
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EU/UK License Management
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Global Regulatory Expertise
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Strategic B2B Pharma Network
Our Core Services
Pharmacovigilance (PV)
- UK QPPV & EU QPPV services
- Local safety officer network in multiple EU territories
- ICSR management & medical review
- Literature monitoring & signal detection
- PSURs, RMPs, and PV system audits
- XEVMPD & MHRA submissions
Regulatory Affairs (RA)
- New Marketing Authorisation Applications (MAA) – UK & EU
- Variations, renewals, and product lifecycle management
- SmPC / PIL updates & readability user testing
- Windsor Framework & Northern Ireland compliance
- Regulatory strategy and agency liaison (MHRA, EMA, CMDh)
Quality Assurance (QA)
- GMP/GDP compliance consulting
- SOP drafting, review & inspection readiness
- Audit management (GMP, GDP, PV audits)
- CAPA management & QA training
Wholesale & RP Services
- UK Responsible Person (RP) support for wholesale distribution
- GDP compliance & quality system implementation
- Supply chain risk management
- Vendor qualification & third-party oversight
Medical Writing & Support
- PSURs, RMPs, ASRs, ACOs
Clinical & non-clinical overviews - Promotional material review
- Technical documentation support
Why Partners Trust VIGIRA
We partner with a wide range of organisations across the pharmaceutical and healthcare sector:
Marketing Authorisation Holders (MAHs)
Full support in PV, RA, QA, and product lifecycle management.
Pharmaceutical Distributors & Wholesalers
RP services, GDP compliance, and supply chain oversight.
Small & Medium Enterprises (SMEs)
Flexible, cost-effective regulatory and PV solutions to help you scale.
Contract Research Organisations (CROs)
Collaboration on safety monitoring, regulatory submissions, and QA systems.
Healthcare Product Companies
Compliance and documentation support for medicines, devices, and borderline products.
What Our Partners Say
"Their flexible approach and deep knowledge made our regulatory strategy much more effective."
"VigiRA Med's expertise in EU regulations helped us navigate complex compliance requirements seamlessly."
"Professional, reliable, and always delivering on time. A true partnership for growth."