About Us

ReMedicas

ReMedicas is a Site Management Organization (SMO), providing expert regulatory, laboratory, clinical, and compliance solutions & services to healthcare product manufacturers. Highly focused on quality to healthcare industry through complete Sincerity. We offer a wide range of solutions & services for Sponsors, Clinical Contract Organizations (CROs), Institutes/ Hospitals and Sites. ReMedicas has over 15 years of experience participating in Global Clinical Research in a wide variety of therapeutic areas. Team has about 20+ years industry experience in handling various levels Clinical Studies in multiple therapeutic areas with multiple clients. Our team is fully qualified, trained and guarantees quality in activities like site management, patient recruitment, and regulatory affairs. At every stage of the product development process, we provide strategic guidance and tactical support to help clients commercialize medical products in the major markets of the world.

We serve global pharmaceutical, CRO, biotechnology and medical device companies across all the clinical trial phases. Our clients demand, and we deliver, world-class results in both Quality and Speed of Enrolments. ReMedicas SOPs meet the foremost ethics & principles for conducting clinical trials. We manage our sites with highly qualified personnel experienced in conducting clinical trials while adhering to applicable regulations, guidelines, and ICH Guidelines.

We know that compromised quality can quickly take your product right back to the starting line. That’s why it’s so important to have a smart strategy from the outset—and why we put it at the forefront of every project.

“Healthcare Quality Through Sincerity”

Our Vison

To provide highest quality healthcare solutions worldwide by supporting progress & spread of global remedies to local citizens

Our Mission

Our mission is to meet your needs in spread of clinical trial industry with provision of both outsourced and household solutions through our expertise, while ensuring that Good Clinical Practice standards and ethics are maintained. It is essential that high-quality data is contributed to the scientific community to create better therapies.

Our Quality Promise

Our mission is to meet your needs in spread of clinical trial industry with provision of both outsourced and household solutions through our expertise, while ensuring that Good Clinical Practice standards and ethics are maintained. It is essential that high-quality data is contributed to the scientific community to create better therapies.

Our Commitment

  • To sponsors and CROs: We are committed to excellence in high-quality management of clinical trials and differentiating your clinical trial data throughout lifecycle.
  • To patients and volunteers: We are committed to providing you a safe and responsive environment, along with the best ethical practices while motivated to improve healthcare treatments outcomes for you and future patients.
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