Managing a Clinical Study Site is no longer cumbersome

Clinical trial conduction can be very cumbersome at times, as it involves regulatory constraints, time constraints and many more challenges. In order to overcome all these you would need a reliable service provider who can handle it all and manage the things. Here we are providing quality services and managing whole of your product's clinical trial. Get in touch with us and take a step towards successful clinical trial.

Right solutions for challenging
clinical trials

Samahitha with its team of efficient and experienced Clinical research Coordinators and
project managers, provides you the best site management services.
Site selection till close out, we take care of all documentation and research operations. All you have to do is come to us!

All You Need To Know About Samahitha

An SMO Operating Pan India

Samahitha Research Solutions is a Site Management Organisation known for its reliable site-related services. With a dedicated, enthusiastic and experienced team of clinical research professionals, we have a broader areas of expertise and hence we keep ourselves flexible when it comes to the services we provide.

Our Vision

To provide value based and remarkable site services across the globe by ensuring the comfort of our employees at the workplace which in turn ensures the astounding quality of the services rendered to the clients.

Our Mission

● To deliver our projects within the stipulated timelines and make sure the quality is never compromised
● To contribute our bit in accomplishing a healthy society with our Good Clinical Practice compliant and trial subject centric work approach
● To stand together and strive for excellence by creating a healthy work environment for our employees

Our site management services include

SMO Operating Pan India

Study Staff Training

We appoint experienced CRCs and study managers at the site for easy and smooth conduction of trials. GCP and study specific Trainings will be provided to all the study staff by our experts.

Site SOP preparation

Site Specific Standard Operating Procedure for Clinical Trials is a must for the conduction of trials. We prepare site specific, GCP Compliant SOPs for smooth conduction of any trial.

Feasibility

Identifying the potential sites and investigators, assist in feasibility assessment and site initiation. Feasibility Assessment directly bring a vital part of the trial, we make sure to provide you with the best and the most feasible sites.

IRB/IEC Related

Assist for faster submission and approval by the Institutional Review board or ethics committee.

We are happy to note that the services offered by Samhitha Research organisation is prompt and timely. Their approach is professional , customer friendly . The service is exemplary ,quick and prompt. Staff are easily reachable and ready to help any time of the hour. Wish them all the best in thier future endeavours.

Dr.Sanjeev B Rai

Chief of Research, Father Muller Medical College and Hospital, Mangalore

We have been in business with samahitha since 2 yrs. I personally wanted to share a quick note that I am glad about our association with samahitha. They have their Network across India with a good knowledge staff. We would like to have our association with you in future also.

Dr.Chandrashekar K

Project Manager, Croissance Clinical Research