Our core team brings over two decades of experience in conducting preclinical studies and commercializing molecules, ensuring top-tier knowledge and expertise for your projects.

We prioritize the confidentiality of our sponsors’ proprietary information and do not undertake in-house R&D in any therapeutic areas where we provide commercial services, guaranteeing no conflict of interest.

DRF’s robust quality management and quality control systems ensure the highest standards in every study we conduct.

Our dedicated innovation team develops and validates in vitro, ex vivo, and in vivo models across multiple therapeutic areas, providing bespoke solutions to meet your specific research needs.

With a deep understanding of global regulatory frameworks, we ensure compliance with international standards, supporting seamless product development and registration.

We are committed to delivering results promptly, with 98% of reports on time and over 80% delivered ahead of schedule. From rapid pre-study responses to swift study initiation, we value and meet your timelines.

We offer technical consulting, including pre-IND & IND recommendations, regulatory review, commercial assessments, and dossier preparation in CTD formats.

We operate as your partner, establishing measurable goals, ensuring alignment on quality and timelines, and providing regular performance feedback to achieve project success together.