Gokula Metropolis Clinical Research Centre is an SMO (Site Management Organization), and endeavours to cater to the growing demands for Clinical Research Trials in India.
Our Goal
To provide you with ethical, quality oriented, enthusiastic, and experienced clinical research sites in an efficient manner.
To help speed up site identification, qualification, initiation, recruitment, retention, budget / contractual negotiations and start up processes whether the trial is managed internally or through a Contract Research Organization.
At our SMO, the internal management and operating procedures are specifically designed to quickly provide you with multiple and highly qualified sites enabling you to choose purely on a best-fit basis. We utilize our database to identify investigators based on your specific criteria, and a good working relationship with numerous international and Indian CROs who may have previously worked with a particular site helps save a significant amount of time and resources during initial site identification, screening, and qualification.
Our Philosophy - Putting People First! Our ICH-GCP trained Clinical Research Coordinators are all experienced and available onsite 24/7. We take great care to ensure that they have all the skills and capabilities required to deliver results that matter. Small wonder then that we have some of the best site management personnel dedicated to bring out the best in our highly trained and experienced clinical trial teams.
Our Promise - No Compromise On Quality We have a Quality and Audit Department that visits every site and audits the study at frequent intervals to ensure compliance with preset norms. Because at our SMO, quality is non-negotiable. Additionally, a Project Manager dedicated to every study ensures seamless functioning by being your single point contact.
Our Focus - Speedier Negotiations At our SMO, we are so focused on cutting down redundancies that even our budgetary and contractual discussions are centralized, thus minimizing lengthy negotiations. In fact, a clinical trial agreement can typically be executed immediately after budget finalization.
WHY GOKULA METROPOLIS
Our core strengths include:
Exclusive professional relationship with two premier, state-of -the- art centres for clinical trials
Extensive database of experienced and trained investigators across all therapeutic areas
Rich network of sites conducive for conducting world class clinical trials
Team of dedicated and motivated Clinical Research Coordinators
Central Laboratory facility
Team of experienced trainers in the field of clinical research And above all, a set of well designed systems and efficient policies to ensure results that matter.
THE GOKULA METROPOLIS CHRONICLE
Gokula Metropolis Clinical Research Centre is a unique Site Management Organization, initiated to cater to the growing demand for clinical research trials in India. In order to keep pace with Global requirements there was a need for -
A Site Management Organization to coordinate clinical trials under strict Global and local regulatory guidelines.
An organization with a commitment to uphold the highest standards of professional excellence, integrity, trust and ethics.
At the Gokula Metropolis Clinical Research Centre, we offer you just that. Our biggest asset is a team of qualified and trained Clinical Research Coordinators who are:
Committed
Dedicated
Motivated
And who insist on delivering accurate and quality results . On time.
We perform in a highly process driven operational infrastructure that ensures ongoing control during and beyond the study period. Our metrics confirm that this results in optimal study speed and quality for our customers. This outcome is attained by organizational controls that begin with the training of our Clinical Research Coordinators, the training & certification of our Investigators and a thorough feasibility analysis of client studies. Controls are then sustained through the pre-study start-up period, the patient enrollment and the patient visit study stages.
This model is more focused in addressing the needs of todays clinical study customers and patients when it comes to time taken and quality of results produced. We believe that we are uniquely positioned to provide results to match our customer requirements.
