Services
What We Can Offer You
From study feasibility to archival, you will experience quality services and best site solutions. The clinical trial unit being the part of a world class multispeciality hospitals and Medical Institutions, the quality of the services are never compromised. Our dedicated team of clinical research professionals work towards providing value based services for phase trials, BA/BE, observational studies and so on! If you are looking for a clinical trial site with the most proactive approach then you are at the right place!
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.
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.
CONTRACT AND BUDGET ASSISTANCE
Efficient Site contract management, cost analysis and budget negotiation for each of the trial that comes to us.
SUBJECT RECRUITMENT
Being the pivotal objective of any trial, the success of any trial depends on the number of subjects recruited after screening the eligibility criteria. Our experienced CRCs and study team will assist you for faster and greater recruitment rate.
INFORMED CONSENT PROCESS
Each subject who is enrolled in the study have the right to know every detail about the clinical trial of which he/she would be a part. The entire process of Informed consent would be assisted by our experienced study staff.
PATIENT CARE
Safety of the patient is the primary concern. Our study staff ensure that proper care is given to the subject. Subject comfort is the priority.
DRUG DISPENSING AND ACCOUNTABILITY
IP storage, handling, dispensing, and documentation of administration, return and/or destruction of the drug.
SUBJECT RETENTION
We make sure that all the subjects randomized complete the study with effective follow up and proper ancillary care.
ADVERSE EVENTS
Effective Detection, recording and reporting of Adverse Events.
CASE REPORT FORMS
Assist for faster submission and approval by the Institutional Review board or ethics committee.
MAINTENANCE OF SITE MASTER FILE
Proper completion and assembly of all the study documents are ensured. We make it easier for you to maintain the site file.
MONITORING AND AUDITING
We conduct internal monitoring in frequent intervals to ensure proper conduction of the trials. With our continuous monitoring, we ensure smooth conduction of the study with minimal or no protocol deviations.
IP MANAGEMENT
We ensure the proper storage and handling of the Investigational Products. Maintenance of IP temperature logs, IP shipment and related logs are all accurately maintained. IP retrieval and destruction are all taken care.
STUDY CLOSE OUT
We ensure faster recruitment and proper completion of all subject files. Make sure that the site is all ready for close out before intimating the sponsor/CRO. Continuous assistance and monitoring will be done to ensure smooth completion of trials.