Clinical Research Training

Altree Healthcare is one of the nation’s leading providers of Clinical Research Training dedicated to promoting ethical and high- quality Clinical Research.

Altree Healthcare recognizes the need for well-trained clinical researchers to bridge the gap between the basic researcher’s bench and the patient’s bedside. Altree Healthcare is committed to result oriented, effective, dedicated management of clinical research training in India.

Indian Healthcare industry has been facing daunting challenges addressing the imbalance in the demand and supply of skill and talented work force. The CROs & Pharmaceutical company of the Healthcare world have been pumping huge amounts for the in-house training program essential for grooming the professional in line with industries’ growing requirements.

At this juncture, Altree Healthcare in association with CROs, Pharmaceutical Companies & MNC’s has developed the concept of Clinical Research Training program strictly adhering to company guidelines.

Altree Healthcare will work with a clinical study center to provide project specific guidance. Altree Healthcare will travel to your clinical center for providing consulting an/ or training to prepare yourself for Clinical Research Trials. Our training sessions are always available at your disposal or let us work with you to customize training schedule that best suits your needs.

To meet the demand of out clients for Clinical Research Professionals, Altree Healthcare selects eligible candidates & trains them in:

  • Clinical Trial Management (Principles & Practices)
  • Pharmacology / Therapeutics
  • Physiology / Anatomy
  • Pharmacovigilance
  • Clinical Data Management
  • Regulatory Affairs
  • Statistics in Clinical Research
  • Soft Skill & IELTS

The training is expected to achieve the following objectives:

  • Obtain a clear understanding of Good Clinical Practice and Standard Operating Procedure for Clinical Research and Clinical Data Management
  • Provide trained professionals to CROs in Bio-IT, Life Science Institutions, Corporates, Academic Research Institutions and / or Clinical Investigators at Hospitals'/Medical Site conducting trials.
  • Provide an understanding of the use of the Electronic Data Capture (EDC) sytem and Project Monitoring in the Clinical Trials process
  • Enable participation in design, conduct and management of global clinical trials, conducted at multi-centric sites in India and Overseas
  • Acquire an understanding of evovling regulatory processes, standards and practice of ICH-GCP in the conduct of different therapeutic trials and in the preparation of submissions to be made to regulatory authorities in India and Overseas