GDP Consultation & Regulatory Guidance
Tailored advice and expert support for GDP strategy, compliance and operations.
Whether you’re building a new pharmaceutical distribution business, expanding to new markets, or navigating a compliance challenge, having access to the right guidance at the right time is critical.
At GDP Pharma Consulting, we offer flexible, expert-led consultancy services covering every element of Good Distribution Practice (GDP)—from site set-up and supplier qualification to IT systems, transport, and regulatory requirements.
Led by former MHRA GDP Inspectors with over 50 years of combined industry experience, we work alongside your team to provide clear, actionable guidance aligned with MHRA expectations, GDP best practice, and business reality.
What We Offer
GDP-Compliant Business Model Design
Build or restructure your pharmaceutical business model to ensure regulatory alignment from day one. Whether you're operating under a WDA(H), WDA(V), or importing under an RPi licence, we’ll help ensure the structure fits MHRA and licencing requirements.
Customer and Supplier Qualification
We can help design and implement risk-based supplier and customer qualification processes, including due diligence, licensing verification, and ongoing monitoring protocols.
Transport and Supply Chain Validation
Whether you manage in-house logistics or outsource to a 3PL, we ensure your GDP transport routes, couriers, and cold chain processes meet regulatory standards and support product integrity.
Export Compliance and International Trade
Navigating GDP obligations across borders? We provide advice on export documentation, trading requirements and the regulatory challenges to ensure your operations remain GDP compliant.
Facility and Infrastructure Design
We advise on everything from warehouse layout and materials handling to refrigeration, HVAC systems, calibration schedules, and GDP segregation, ensuring your site is inspection-ready and operationally efficient.
IT and Document Control Optimisation
We assess your document control system, eQMS platform (see our QMS service & TraxQM), and digital infrastructure to align with GDP principles and MHRA expectations.
When to Engage Us
WDA application or licence expansion
SOP and QMS review projects
Transport or warehouse setup planning
New product category, import route, or service launch
Preparation for MHRA inspection or post-inspection CAPAs
Long-term strategic quality and risk planning
Whether you need one-off advisory or ongoing consultation, we will work flexibly around your team’s needs and timelines.
Ready for Specialist GDP Advice?
Let our team support your business with targeted guidance across every GDP touchpoint.
Phone: 07309 095922 or 07309 094743
Email: admin@gdppharmaconsulting.co.uk