From Site Initiation To Site Closure:
We offer site management services delivered through a prudent and highly experienced team. We provide services from site initiation to site closure.
To Train Our Employees:
We train our people to work carefully to track the all project in proper time guidelines and accordance to requisition.
We train our employee comprehensively to give there best to the industry.
Selection Of Employees:
We select employees very carefully and train them intensively so that we may follow the high standards of clinical research services.
The Knowledge Of The Local Language & Work Culture:
Knowledge of the local languages and work culture to provide the extra level of services.
Maintenance Of Standard:
We maintain the class of work right from the investigator site selection to the managing the data after the site close out.
We Are Expert:
We are expert in clinical trial supply management, early study indication and approvals from the regulatory authorities.
Help In Enrollment Of Patients:
Our coordinators assist in smooth and quick enrollment at the site.
We manage and observe a cleaner data generation from site. The time management and to follow the requirement of regulations is our key agenda.
The requirement of regulatory authorities is being fulfilled by managing and observing a cleaner data generation from the sites.
Data Protection and data exclusivity is the main recognition of us.
Strong leadership and an environment of commitment and responsibility make us a diamond in the fraternity.
Follow Of ICH & GCP Guidelines:
ICH and GCP are the main tools with which our all professionals are equipped with.
Our post competitiveness in the services is highly appreciated by our clients.
Managing the financial agreement between the parties is the key feature of us.
The Well Being Of The Patients:
Our coordinator is not only coordinating in the site and sponsor but managing the site for the well being of the patients.
✓ In current we have four multinational multicentric projects in different therapeutic areas.
✓ Two multinational project in nephrology.
✓ CME on Renal Cell Carcinoma.
✓ To foster and encourage cooperative clinical research.
✓ To participate in all phases of clinical research upholding respect for individual patients.
✓ To generate data that is of high quality, ethical, complies with GCP and other regulatory and statutory bodies, authorities.