Welcome to Raptim Research Pvt. Ltd.!

Raptim, a global independent and internationally accredited Clinical Research Organization (“CRO”), established in 2005, supporting the end-to-end services under the Clinical Research domain - Bioequivalence, IVRT/IVPT & BCS Biowaiver option; for all Pharmaceutical companies worldwide.

Raptim stands for “Rapid” and it acts as a catalyst to hasten the regulatory submissions and approvals of customers’ products. We are market leader among independent Indian CROs, with the highest quality standards and quick turnaround times. We have a strong regulatory track record and numerous accreditation/approvals from global regulatory agencies like USFDA, WHO, ISP Chile, NABL, DCGI & product approval from MCC, CANADA. TGA, MHRA and FDA-Korea.

Raptim is a technologically advanced CRO with experienced professionals who apply innovative tools and processes to their clinical development. We believe that our experience in all aspects of clinical research management; places us in a unique position to assist Sponsor with unparalleled support.

Services include end to end verticals as below:

•	BA/BE studies
•	Bio analytical services (Drug, Elemental, Vitamin, Hormones etc)
•	Dermatology
•	IVRT/IVPT
•	CACO2 studies
•	Patient Pk studies
•	Clinical Trial (phase-II – IV)
•	Long housing study - Phytonadione, KCL 
•	Data management
•	Medical & Scientific Writing
•	Complex BE Studies - Controlled substance, Inhalation, Nasal Spray, Transdermal Patch, Suppository, female contraceptive ring, Hormonal study.

Headquartered & operations in Navi Mumbai, and Business offices in INDIA and USA with employee strength of 350+ of varied ethnic backgrounds providing a culturally rich working environment. Raptim has the optimized resources and the right approach to deliver the results that will make the project a success.

New state of the art clinical research facility, coming soon!!

Contact US: contact@raptimresearch.com

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Raptim Research Pvt. Ltd.

Raptim Research Pvt. Ltd.'s headquarters in Mumbai, India

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