ProRelix Research Information

ProRelix Research is a leading Contract/Clinical Research Organization (CRO) with offices in the USA and India along with site networks in Europe and Southeast Asia supporting the clinical development of innovative new healthcare inventions and innovations to improve the health of patients. We deliver prompt reliable and ethical clinical trials accelerating your drug development journey with precision flexibility and trust. Since 2015 we have partnered with pharmaceutical biotechnology and medical device companies to deliver high quality end to end clinical research services on time and within budget. Why Sponsors Choose Us: → Extensive global site network across USA, India, Thailand, South Africa, Denmark, Poland, Bulgaria, and Australia etc. → Strong presence in USA and India. → Dedicated Pharmacovigilance and Regulatory team. → Proprietary Decentralized Clinical Trial platform. → Successfully delivered multi country clinical trials. Clinical Research Services Includes: → Clinical Trial Services (Phase 1 to 4): Project Management, Site Selection & Feasibility, Regulatory Affairs, Clinical Operations & Site Management, Vendor Management, and Patient Recruitment & Retention. → Medical Writing → Clinical Data Management → Biostatistics → Clinical Trial Medical Monitoring → Clinical Trial Site Monitoring → Clinical Safety → Trial Master File (TMF) Management Our Portfolio Includes: For Regulatory Submission: New Drug, Repurposed Drug, Biological & Biosimilar, Bioequivalence, Hybrid & Decentralized, Personalized Medicine, Stem Cell Therapy, and Medical Device trials For Claims Support: Investigator-Initiated Trials (IITs), Real-World Evidence (RWE), Herbal, and Nutraceutical trials Therapeutic Expertise In: Oncology, CNS (Pain & Psychiatry), Autoimmune/Inflammation, Cardiovascular, Ophthalmology, Endocrinology/Diabetology, Dermatology, Respiratory & Other areas Get expert CRO support for your next clinical trial. Email Us: info@prorelixresearch.com