A Clinical research is a scientific study of the effects, risks, efficacy and benefit of a medicinal product. These are carried out prior to the release of the medicine in the market. These trials are undertaken at various stages and studies are conducted after the launch of a new product to monitor safety and side effects during large-scale use. Clinical trials are conducted by Pharmaceutical companies or Contract Research Organization (CROs) / Site Management Organization (SMOs) on their behalf.
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20
Years of exps
Site Management Services
Medrix Clinical Research site management organization (SMO) was created to fill an unmet need for quality site management Services for clinical trials industry in the North India region where Medrix Clinical Research already has several years of experience undertaking CRO projects.
The SMO trains and provides Clinical Research Coordinators (CRC’s) as well as other cadres of site support staff who will support clinical trial investigators especially in small clinical trial sites and doctor’s clinics with site feasibility, Site Selection process, Regulatory/IRB support, patient recruitment, enrollment and follow up, close out and Study Records Archival.
Record Management Services
We are providing end to end physical Documents Storage solutions, which if implemented can help you to map the overall record storage scenario within your organization, thus resulting in quick decision making, elevated organizational efficiency and higher productivity. Our Record Management Services are cost-effective and can be customized as per your needs and requirements.
Equipment Calibration Services
Medical Equipment Calibration is carried out to minimize the uncertainty in measurements, reducing errors and bringing measurements to an acceptable level. With repeated use and over a period of time, all equipment begins to degrade and that affects its accuracy and precision. Regularly calibrating equipment will ensure that industry defined standards are met and that the equipment is functional thus providing accurate output.
OUR AMENITIES
Insourcing
Because Clinical Research is conducted in a dynamic environment, it is important to ensure we have sufficient manpower.
Medical Writing Services
We understand the complexity and importance of Medical writing and to provide this service we have the experts for preparation of scientific documents.
Regulatory Services
Medrix Clinical Research regulatory Services can assist sponsors through the varied local regulatory and ethical requirements to ensure the most efficient start-up of a clinical trial.
Training
Medrix Clinical Research conducts training programs , Ethics in Clinical Research and ( ICH - GCP ) Good Clinical Practices in Clinical Research for all levels of site staff .
Our Client
Testimonials
What Our Clients Say?
They are one of the best Services providers in this industry and I am fully satisfied with them.
Team Medrix has been an expert of their field and the way they do their job is highly appreciated.
