Responsible Person (RP) Services
For pharmaceutical and biotech companies seeking to distribute medicinal products in the European Union, appointing a qualified Responsible Person (RP) is a regulatory requirement. The RP role demands comprehensive knowledge of EU pharmaceutical legislation, GDP compliance, batch release protocols, and pharmacovigilance obligations. Many organizations struggle to maintain in-house expertise, particularly when expanding into new markets or managing diverse product portfolios. Inadequate RP oversight can result in regulatory sanctions, product recalls, supply chain disruptions, and delayed market entry.
Our Responsible Person services provide pharmaceutical and biotech companies with experienced, fully qualified professionals who serve as your designated RP across EU member states. We assume full regulatory accountability for your products, ensuring every batch meets quality standards and regulatory requirements before release to the market. Our team maintains current knowledge of evolving EU regulations, conducts rigorous quality assessments, and manages all documentation requirements with precision and efficiency.
We handle the complete spectrum of RP responsibilities, including batch certification, GDP compliance verification, import/export coordination, regulatory authority liaison, and maintenance of comprehensive distribution records. Whether you need RP coverage for a single market or across multiple EU territories our offerings are scalable.
We are Cost Effective. Avoid the expense of hiring, training, and maintaining full-time RP staff. Access expert-level service without overhead costs.
Contact us today to learn how our Responsible Person services can accelerate your European market strategy and ensure seamless regulatory compliance.
