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Site Solutions

Clinsol work as a partner for Sponsors and CROs to address site level challenges and trial level challenges with our networked site and patient database, and we provide customized site management services. As a practice we enable sites with tools, Process, and techniques to perform to their best potential, and we achieve trial success through these services.



    Clinsol offers following mentioned services:

  • Onsite Trial Management
  • Serve as Single point of contact (POC) for the Sponsor and/or CROs & functions as centralized administrative, Contract, financial and project management team
  • Accelerate the timeline and productivity in study start up, conduct, and close out
  • Patient recruitment support to site: We take a proactive approach to develop a strategic enrollment plan that is patient centric, Therapeutic data driven, and site specific.
  • Support sites to enroll the appropriate patients in your study in the shortest possible time.
  • Efficient start-up communication with the Institutional Ethics Committee/Institutional Review Board (IRB) of respective site.See More
  • Clinical trial staff support, Qualified, well trained Clinical Research Coordinators to provide patient counseling and comprehensive study support.
  • Retention strategies, we collaborate with Clinical Investigational sites to retain the study subject by providing the required support to minimize the drop out
  • Data Acquisition: Provide required support and ensure quality data transcribed on to CRFs, and other relevant essential documents.
  • Therapeutic area expansion: Provides guidance on therapeutic area for expansion at each network sites
  • Site Staff Training: Provide the required training programs to educate the site staff, including protocol amendments
  • Compliance: Continually monitors the sites to ensure the protocol compliance at all stages of the study and alerting investigators of potential protocol violations and ICH-GCP violations

    Therapeutic Area

    Clinsol deep therapeutic knowledge and understanding of the key issues combined with clinical development experience drives more effective and efficient pathways, whether Customers are in clinical development, launching a product or are managing a portfolio across the development and product life-cycle, our expertise enables Customer team to minimize uncertainties.

    Clinsol has experience across all the major therapeutic areas (Including but not limited to the following).


  • Oncology
  • Cardiology
  • Endocrinology
  • Dermatology
  • Urology
  • Gynecology
  • General Medicine
  • Anesthesia
  • Orthopedics
  • Hematology
  • Critical Care
  • Neuropsychiatry
  • Vaccine
  • Gastroenterology
  • Medical Device
  • Pulmonology
  • Neurology
  • Psychiatry

    Experience

    • Our site team has an experience of conducting clinical trials in 19+ major therapeutic areas.
    • We have successfully closed out 5+ global clinical trials with in last
      3 FY.
    • Our team has experience in medical device clinical validation studies, conducted for submission to US-FDA and other major regulatory bodies.
    • Clinsol site team has successfully completed 4+ Phase-II, 24+ Phase-III, 19+ phase-IV clinical trials without facing any major audit findings from Sponsors and CROs, in last 5 FY.


    Our dedicated sites:

South India :
  • Bangalore
  • Hyderabad
East India :
  • Bhubaneswar
  • Kolkata

54+

Completed Projects

16+

Sites

80+

Networked Principal Investigator

19+

Therapeutic Area