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Remed Research

WELCOME TO REMED RESEARCH SOLUTIONS Pvt. Ltd

We as a Site Management Organization engaged in the service of providing suitable sites and the patient pool to our clients to carry out Clinical trials of new/ marketed drugs.

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ABOUT US

ReMed Research Solutions Pvt. Ltd is a Site Management Organization. We are involved in dealing with all clinical trials from Phase I to Phase IV. We're committed to providing and managing clinical sites with GCP compliance, ICH-GCP experienced certified medical practitioners & trained clinical research staff.
ReMed Research is having its wide branches of services in the healthcare sector. ReMed Research acts as Clinical Trial Implementer at various trial sites all over India and coordinates for trial implementation with CRO or Sponsors from Pharma / Biotech companies.

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OUR MISSION

We keep a vision of becoming the first choice for our community organizations as a Site Management Organization through our consistent efforts to provide transparency and sincerity in our services with integrity by all means in a business. Our work should be dedicated and beneficial for the betterment of mankind, pharmaceutical companies, and CROs.

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WHAT MAKES US SPECIAL

COMPASSIONATE TO PATIENTS

We try to understand the sufferings of the patients and focus on handling them with care and love by keeping their safety in mind.

ELIGIBLE PATIENTS POOL

At ReMed Research our efforts are to provide you with the most eligible patient pool as per your study requirements and criteria..

REPEATED SCRUTINIZING

We understand how important the correct and fair data regarding trial results are. We try to scrutinize it as much as we can to nullify the errors.

DETAIL ORIENTED

It is a well-known fact that even a minute detail can change the game significantly. Along with the conspicuous observations we tend to focus on minute things also to provide the most fair results

OUR SERVICES

As a Site Management Organization, we are glad to offer the following services to our clients as per their needs.

CLINICAL OPERATION SERVICES
Study start-up at potential sites with a good patient pool. Feasibility of studies and initial document preparation at site level.
Subject recruitment and follow-up..
MANPOWER MANAGEMENT SERVICES
We provide proper trained Clinical Research Coordinators, Study nurses, and Phlebotomist to SMO, CROs, Sponsor, Institute and Investigator
CLINICAL DATA MANAGEMENT
We provide data entry management as per Sponsor/CRO requirements with ICH GCP guidelines, including data entry in paper CRF or eCRF on a fast-track process.
Document archival facility as per regulatory guidelines.

WHY CHOOSE US

We as a Site Management Organization engaged in the service of providing suitable sites and the patient pool to our clients to carry out Clinical trials of new/ marketed drugs.