Strategic outsourcing solutions for GMP & GDP Quality and compliance
Accelerate your market access across the UK and EU with a unified regulatory gateway.
In a complex regulatory landscape, maintaining a fully functioning Pharmaceutical Quality System (PQS) often presents a significant administrative and financial burden. Managing diverse portfolios usually requires coordinating multiple providers, adding friction to your supply chain.
Our Integrated Importation & Compliance Solutions
By aligning our multi-sector expertise, we remove logistical friction and ensure your products benefit from the same rigorous, unified QP and RP oversight.
Qualified Person (QP) Services & MIA Support
Leverage our EU MIA and UK MIA for human medicinal products. We provide scalable support for batch certification, release, and third-party manufacturing oversight.
Responsible Person (RP/RPi) & GDP
Expert oversight for your Wholesale Distribution Authorisation (WDA). We ensure your supply chain remains inspection-ready and compliant with all Good Distribution Practice requirements.
IMP Importation & Clinical Materials
With our EU MIA(IMP) licence, we provide specialist importation and certification of Investigational Medicinal Products, ensuring clinical materials reach trial sites efficiently across the EEA.
Veterinary Solutions (VIA & ManA)
Comprehensive importation support for Veterinary Medicinal Products into both the EU (VIA) and the UK (ManA), maintaining high compliance standards across your entire animal health range.
Comprehensive Audit Programmes
Targeted GMP and GDP audit services designed to identify risks, strengthen your quality systems, and protect your technical compliance.
Why consolidate with PLG?
We bridge the gap between regulatory expectation and operational reality. By integrating our five licences, we deliver simplified oversight, cross-border logistical efficiency, and a robust framework designed to scale with your portfolio.
Use the form below to start a discussion about how we can start supporting you.