RP & QP Services (UK & EU)
Responsible Person and Qualified Person support to strengthen oversight, ensure compliant release, and provide inspection-ready assurance
TDP provides UK and EU Responsible Person / Import (RP) and Qualified Person (QP) consulting services to support regulatory compliance, batch certification, and market supply obligations across EU and UK regulatory frameworks. Our services are delivered by elite RP and QP professionals with extensive hands-on experience navigating complex pharmaceutical and life sciences supply chains. While our methodology is product-agnostic, we provide deep, specialized expertise tailored to your specific requirements through our network of subject matter expert (SMEs).
These services are delivered with a strong emphasis on governance, transparency, and integration. TDP’s RP and QP consultants work as a seamless extension of client quality and regulatory teams, providing independent oversight that protects patient safety, ensures continuity of supply, and stands up to regulatory scrutiny from authorities including the MHRA, EMA, and EU Competent Authorities.
Our approach combines technical depth with practical delivery, ensuring compliance is not only achieved on paper but embedded into day-to-day operations.
BEST FOR
Companies needing RP support for GDP oversight and ongoing compliance
Organisations requiring QP oversight for batch certification and release activities
Teams needing experienced support ahead of audits, inspections, or scale-up
WHAT’S INCLUDED
RP support and guidance aligned to GDP expectations
QP oversight support (scope defined to your operating model)
Quality governance and decision support with clear written rationale
Review of documentation required for compliant release decisions
Audit/inspection readiness input related to oversight responsibilities
Stakeholder coordination (manufacturers, QA, supply chain)
Practical recommendations that can be implemented immediately
HOW IT WORKS
Confirm scope (RP, QP, oversight model, frequency)
❶
Agree deliverables and reporting cadence
❷
Delivery and documented outputs
❸
Ongoing support or transition as required