About Us
All You Need To Know About U
All You Need To Know About U
All You Need To Know About U
Clini Med Biotech 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
All You Need To Know About U
All You Need To Know About U
To provide value based and remarkable site services across the globe by ensuring the comfort of our team which in turn ensures the astounding quality of the services rendered to the clients.
Our Mission
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Our Strength
● 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 Team
Our Strength
All You Need To Know About U
Our Strength
● Experienced team of Investigators
● Pool of Experienced sites across the country
●Dedicated and experienced Site Coordinators
Our Services
We, with Our dedicated team of Clinical Operations experts provide site management services for phase trials, BA/BE, observational studies and what not!
If you are looking for site management services with the most proactive approach then you are at the right place!
Yes, we at Clini Med Biotech, have an extraordinary team of experienced Site and Clinical Research coordinators and assure to provide you the best site services you can ever experience.
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 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.
Contract and budget assistance
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.
Assist for faster submission and approval by the Institutional Review board or ethics committee.
Contract and budget assistance
Subject recruitment & Subject retention
Contract and budget assistance
Efficient Site contract management, cost analysis and budget negotiation for each of the trial that comes to us.
Subject recruitment & Subject retention
Subject recruitment & Subject retention
Subject recruitment & Subject retention
Our experienced CRCs and study team will assist you for faster and recruitment rate. We make sure that all the subjects randomized complete the study with effective follow up and proper ancillary care.
Case report forms
Subject recruitment & Subject retention
Subject recruitment & Subject retention
Accurate CRF filling, handling and maintenance is assured. Our CRCs are trained and experienced to work on EDC based Data Management platforms.
Maintenance of Site Master File
Drug Dispensing and accountability
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.
IP Management
Drug Dispensing and accountability
Maintenance of Site Master File
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
Drug Dispensing and accountability
Drug Dispensing and accountability
Drug Dispensing and accountability
IP storage, handling, dispensing, and documentation of administration, return and/or destruction of the drug
Adverse events
Monitoring and Auditing
Drug Dispensing and accountability
Effective & Timely recording and reporting of Adverse Events per applicable regulations
Monitoring and Auditing
Monitoring and Auditing
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.
Study close out
Monitoring and Auditing
Monitoring and Auditing
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.
Contact Us
Email: clinimed23@gmail.com
Call :+91 9696801196
