Clinical Research Services

Our Services Include:

For Sponsors, CROs or SMOs -research
  • Site Identification
  • Signing of Confidential Disclosure Agreement (CDA) from PI 
  • Completion of study specific Site Feasibility Questionnaire 
  • Clinical Trial Agreement finalisation with Site authority & PI 
  • Ethics Committee Submission
  • Assist with obtaining approval from Institutional Ethics Committees
  • Managing subject recruitment 
  • Study Specific Site/Clinical Research Coordinator support
  • GCP & Other Regulatory Training
  • Regional CRA or Independent Monitoring service 
  • Independent Audit service 
  • Providing Independent archival facility
For Sites & Ethics Committee
  • IEC Registration or Re-Registrationdrug-testing-pharama-trendz
  • NABH Accreditation of IEC/IRB
  • IRB/IEC SOP Development
  • Site SOP Development
  • Accredited Local Lab services
  • Regulatory Guideline training for IEC Members & Site Staff

"Our CRCs are experienced in Oncology, Critical Care, Gastroenterology, Vaccine, Pulmonology, Dermatology, Infectious disease, Rheumatoid Arthritis, Osteoarthritis, Cardio Vascular,Psychiatric, Diabetes, Hypertension, Orthopedics and others indications."

Why We ?
  • Also experienced in PK,BA-BE,IPD & OPD studies 
  • Experienced in Pharmaceuticals, Biologicals & Nutraceuticals products.
  • Experienced in Both Global & Indian Trials 
  • GCP & Other regulatory guidelines trained. 
  • Pre-screening of subjects according to protocol specific Inclusion & exclusion criteria before study initiation. 
  • Well versed with paper based CRF & eCRF, site trial master file maintenance and proper source documentation to complete monitoring or audit in time. 
  • Supporting PIs in every aspects of the trial for smooth running of the trial at the site. 
  • Reporting AE/SAE in regulatory time lines. 
  • Developing new potential sites for conducting clinical research. 
  • We maintain high degree of confidentiality about the ongoing and new projects among all parties. 
Our Unique Service For Patients
  • Clinical research includes trials that test new treatments and therapies as well as long term natural history studies, which provide valuable information about how disease and health progress.
  • These are conducted  both in Private and Government hospitals across India.
  • Subjects (Patients) are the biggest beneficiary among all the stakeholders in Clinical Research.
  • With the registration and accreditation of Institutional Ethics Committee, subject will get high quality of care & safety.
  • The subjects are serviced by credential medical staff under the proper supervision of the Investigator.
  • Rights and welfare of the subjects are respected and protected including confidentiality of their identification.
  • Patients can voluntarily participate or withdraw from the research related treatment after discussion with the doctor.
  • Possible Benefits of clinical research;
  • Introduction of more effective therapies in addition to those currently available
  • Additional quality medical care compared to non-participants
  • Close Monitoring for Possible negative effects or Risk
  • Treatment, Lab test, Medical Check ups are available FREE OF COST
  • More personalised care in Govt. Hospitals & Renowned Multi/Super Speciality Hospitals
  • Aid in new research that may result in Significant medical advances
  • Possible Risks of clinical Research
  • New Treatment may not be as effective as standard treatment
  • Unexpected and possible side effects 
For Other Queries You can Contact us at
  • Our motto is to provide the information to the patients, who are interested to take the possible therapeutic benefits of new treatments.
  • We will provide the hospital and Principal Investigator (Doctor) details for the respective disease or Indication
  • We request other Health Care Professionals visiting this page to guide the patients to get benefits of research treatment.
    • Name 
    • Contact No.
    • Email 
    • location
    • Disease type 
Request to provide above details, So that we can provide you the necessary information in 7 working days.
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