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We provide end-to-end Early stage drug discovery (BABE and In-vitro) and Late stage (Phase I to IV) clinical trial management services, bioanalytical testing, post-marketing surveillance and regulatory support for biopharmaceutical and medical device companies worldwide. We offer a comprehensive range of services. Our global reach and expertise span multiple therapeutic areas, providing tailored solutions for biopharmaceutical and medical device companies that meet/exceed your expectations.

Our expertise spans over 18 therapeutic areas, including Oncology, Endocrinology, Cardiovascular, CNS, Dermatology, Immunology, and Vaccines. We support Biopharmaceutical drugs and device development across a wide range of indications. We offer both clinical and analytical support across all phases of drug and medical device development.

Yes, we have extensive experience in managing global clinical trials, ensuring 100% compliance with international regulatory standards. Our global presence allows us to offer localized solutions while maintaining a unified / Global approach to project management and delivery.

You can reach out to us (request a proposal or schedule a consultation) via the contact form (Page) on our website or contact us directly via email at [contact@raptimresearch.com] or phone. One of our business development representatives will respond promptly to discuss your specific needs and how we can support your project.

Yes, we offer comprehensive regulatory support, including documentation preparation, submissions, and regulatory strategy development, ensuring your product meets all necessary global, local/regional requirements. We adhere to the highest international regulatory standards, including those set by the FDA, EMA, and WHO. For more detailed information on our regulatory support services and compliance track record, please contact us directly or visit the Regulatory Services section of our website.

We operate globally, with a network of facilities and teams strategically located across North America, Europe, Asia, Middle East, Australia and Africa. This enables us to provide localized expertise while ensuring compliance with international regulatory standards.