ProRelix Research is a Clinical Research Organization (CRO) with offices in the USA and India along with site networks in Australia, Thailand, Africa, and Europe supporting the clinical development of innovative new healthcare inventions and innovations to improve the health of patients. Every project is equally important to us. We first listen to you and strategize, aiming to a long-term partnership. We understand each project is unique on its own, and conscious clinical development, where efficiency is utmost and accuracy is supreme, is valuable and demanding to long-term success.
We provide services to help pharmaceutical, medical device, biopharmaceutical and nutraceutical/ herbal companies to transform scientific discoveries into new treatments. From clinical trial services, clinical data management services, pharmacovigilance services, medical writing services, drug regulatory affairs services, decentralized clinical trial services to leveraging real world insights, our therapeutic, technical, & operational ability is underpinned by a great conviction in what we do.
ProRelix Research has a global network of distinguished scientific leaders who are experts in a diverse range of therapeutic areas. We specialize in chronic diseases clinical trial services including oncology, respiratory, ophthalmology, endocrinology, immunology, dermatology, etc. Our reputation in clinical research services differentiates us from conventional clinical research organizations (CRO). We leverage our scientific leadership to establish and maintain the engagement of unique investigator networks for clinical research services.
As an esteemed clinical research company in India, we are dedicated to delivering high quality trials individualized to meet the needs of our clients. Our extensive experience also positions us as a trusted clinical research company in the USA, where we collaborate with top-tier firms to advance medical research.
Strategic clinical trial services serves as a cornerstone in advancing medical research and development. ProRelix Research features holistic clinical trial services in India and globally, including the Clinical trial services in the USA. With expertise in managing Phase 1, 2, 3, and 4 clinical trials, ProRelix Research supplies specific solutions such as bioequivalence clinical trial services and nutraceutical clinical trial services. As a prominent CRO for clinical trials in India, ProRelix ensures high-quality data management and regulatory compliance, making it a trusted clinical trial company in India. our commitment to excellence is evident in personalized plans that enhance the efficiency of clinical trials across various therapeutic areas.
Clinical trials play a pivotal role in the approval of new drugs as they most accurately reflect the effect of the drug in the human body. Since drug development is a costly and laborious process with the clinical trial phase...
Medical devices are an integral part of our lives from a simple thermometer to a life-saving pacemaker. Devising medical device clinical studies is complex and requires knowledge and experience-our experts at ProRelix Research can help you design studies depending upon...
The use of software to inform healthcare decisions is ubiquitous and is being utilized by patients, clinicians, and healthcare providers. Proper understanding, planning, and design of SaMD is essential for approval. ProRelix Research provides customized solutions and helps you adapt...
The success of a generic drug or biosimilar often hinges on the results of bioequivalence studies making it essential to partner with an experienced and reliable CRO to design and conduct bioequivalence studies. ProRelix Research offers full range service for...
ProRelix Research offers customized, end-to-end services for clinical trials of a broad range of biological products to help bring both innovator biologics and biosimilars to the market in a timely and cost-effective manner. We ensure compliance with regulatory requirements in...
The exponential growth in the natural product and dietary supplements field requires clinical trials to support safety and efficacy. ProRelix Research lends support at every step of your clinical trial journey to help you carve a niche in the dietary...
Diagnosis of diseases by clinicians using suitable tests guides treatment decisions and is necessary for improving and prolonging the health and well-being of patients. ProRelix Research partners with you to provide clinical trial support and ensure your device meets regulatory,...
ProRelix Research provides tailored end-to-end management of clinical trials keeping cost and patient safety at the forefront. We help you navigate the complex path of clinical trials by offering study support from patient recruitment to statistical interpretation to help you...
At ProRelix Research we understand that realization of the full potential of the emerging field of personalized medicine is dependent on the design and execution of clinical trials. We can help you circumvent the unique challenges associated with conducting precision...
ProRelix Research understands the utmost importance of protecting patient safety from clinical trials to real-world use of a new drug, biological or medical device. We help you develop appropriate pharmacovigilance plans and adverse event reporting systems in compliance with US...
Our experts at ProRelix research provide customized and comprehensive pharmacovigilance and safety monitoring programs in accordance with European Union (EU) regulations with an emphasis on patient well-being from research and development to post-market authorisation.
Patient safety and well-being lie at the heart of all our pharmacovigilance operations at ProRelix Research. We are with you every step of the way-from development of a pharmacovigilance system to regular reporting of safety and adverse events to regulatory...
The successful execution and completion of a clinical trial are determined by several interconnected cross-functional expertise teams, including Medical Writing, Regulatory Affairs, Clinical Project Management, Clinical Data Management, Site Management, and Patient Recruitment, Faster Ethics Committee Approval, Pharmacovigilance, and much more.
A Quality driven Global Clinical Research Organization (CRO) that can truly understand your needs and help you to achieve your goals by minimizing the complexity across functional teams. We at ProRelix Research strive to bring forth the best clinical research services managed by therapeutically sound experts and professionals who are having over a decade of international regulatory experience in conducting complex clinical trials into simple ones.
Also, our extensive knowledge, quality work, and global recognition make us an ideal choice for the rising demand for conducting holistic clinical trials which include New/ Repurposed Pharmaceutical Products, Biological, Herbal, Nutraceutical, In Vitro Diagnostic Devices, Therapeutic Medical Devices, and more.
We are dedicated to follow the best ethical and clinical practices when conducting clinical studies while keeping the safety of all of our participant at core. Our motto is to provide our clients with prompt clinical study management, reliable clinical data with integrity, and ethical conduction of the clinical trials. The uniqueness of our services and functionality is that we not only design the ideal mechanism for better functionality of your trials but we also provide you a lending hand in all those processes and take you through them from the start till the end to reach your goal.
Our service portfolio includes Clinical Trial Project management, Phase 1 to 4 Clinical Trials, Drug Regulatory Affairs, Medical Writing, Clinical Data Management, Pharmacovigilance, Clinical Operations, etc. We are open to clients from all over the world and have a strong presence in USA and India and strategic partners in Europe, Australia. Let’s commit ourselves to better healthcare systems all around the world by ethical, prompt, and reliable clinical research studies!
At ProRelix Research we are a team of experienced people who are well aware…
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ProRelix Research’s medical writing service capabilities range from Clinical Research, Regulatory…
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ProRelix Research’s Regulatory Affairs services provide expert support in drug development programs.
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Medical device clinical trials in India for CE marking are integral to ensuring compliance with European Union (EU) standards, enabling manufacturers to access the lucrative European market. The CE marking […]
FDA Validation Rules for Submission Data are essential for regulatory compliance. Learn about FDA data submission requirements, validator rules, study data standardization plans, and Pinnacle 21 validation. Stay updated with […]
Integrating E-Clinical Technologies in smarter clinical trials improves efficiency, enhances data accuracy, and streamlines clinical research for better patient outcomes. With the increasing world population, clinical trials are now more […]
I would highly recommend Prorelix Research as a client‐focused company with a strong patient database that delivers on its promise to deal with patient recruitment.
We selected the Prorelix Research because of its comprehensive nature, flexibility and reliability. We were happy as ProRelix Research proved to be a best solution to our clinical trial operations.
We are very happy to have found Prorelix Research, during our relationship, ProRelix Research has delivered best services for our medical device study project..
The quality of the service provided by ProRelix Research matches the sophistication of their services platform. Their services have helped us thoroughly and promptly.
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