Supply Chain
NovaPharm Healthcare operates an end-to-end regulatory-first supply chain — from EU-GMP supplier qualification and MHRA PLPI regulatory filing through to cold-chain distribution, last-mile delivery, and active pharmacovigilance. Every step is documented, auditable, and fully GDP-compliant.
How It Works
Our supply chain is built around regulatory compliance at every stage — ensuring that every product we distribute meets the highest standards of quality, safety, and traceability before it reaches a patient.
Every supplier undergoes a structured qualification process before entering our network.
All products are fully documented before they move in the supply chain.
End-to-end MHRA Parallel Import licensing managed by our regulatory team.
Temperature-validated storage and distribution for all product categories.
Reliable final delivery with full regulatory documentation compliance.
Active post-market surveillance integrated with MHRA reporting requirements.
Regulatory Note: All products distributed by NovaPharm Healthcare are sourced exclusively from EU-GMP verified suppliers and handled under full GDP compliance. MHRA WDA(H) application is currently in progress. Full regulatory documentation is available to qualified customers on request. Contact: vishal@novapharmhealthcare.com
Infrastructure
Our supply chain infrastructure combines specialist third-party logistics partners with in-house regulatory and compliance capability — ensuring consistent quality and traceability at every point.
Specialist pharmaceutical cold-chain partners with temperature-sensitive distribution expertise. Real-time monitoring, validated packaging, and environmental logging ensure product integrity from origin to point of dispensing.
Multi-territory pharmaceutical logistics capability covering Europe and the United Kingdom. Partners hold relevant pharmaceutical distribution licences, hazmat certifications, and GDP-compliant operating frameworks.
Dedicated regulatory and pharmacovigilance function with GxP-compliant systems, MHRA-integrated adverse event reporting, and batch traceability management. For pharmacovigilance enquiries: pv@novapharmhealthcare.com
Services
Our integrated service model delivers pharmaceutical supply chain value across multiple revenue streams — combining direct distribution, regulatory advisory, and licensing partnerships under a single operational framework.
Direct supply to NHS trusts, hospitals, independent pharmacies, and licensed wholesalers. Wholesale pricing structures with volume-based frameworks and institutional procurement support.
A growing portfolio of MHRA-licensed and PLPI-compliant pharmaceutical products across oral, liquid, and other dosage forms — serving a broad range of therapeutic categories.
Full end-to-end MHRA PLPI application management — including documentation preparation, PIL translation and localisation, labelling compliance, and ongoing MHRA reporting obligations.
Integrated cold-chain logistics, batch traceability, pharmacovigilance support, quality documentation management, and compliance audit services — available to qualified partners.
End-to-end UK market entry support for EU-GMP manufacturers — covering regulatory pathway mapping, MHRA PLPI filings, compliant packaging and labelling, and NHS distribution onboarding.
Commercial out-licensing and regional distribution agreements, structured under clearly defined contractual frameworks with agreed service levels, royalty terms, and escalation protocols.
