We provide training in clinical research and medical writing.


The team provides training program on all aspects of drug development and research activities to the various stakeholders in clinical research and drug development. The key areas covered include:

● ICH GCP guidelines
● Drug development process
● Clinical research
● Audits and inspections
● Ethics Committee and investigators responsibilities
● Roles and responsibilities of CRC (Clinical Research Coordinators)
● Regulatory laws and guidelines – global and Indian
● Recent amendments and revisions.


Members of our medical writing and editing team have extensive experience in conducting medical writing training through lectures, webinars, and workshops. Our experts have conducted medical writing training at the annual conferences of DIA (India), Indian Society for Clinical Research (ISCR), Indian Cooperative Oncology Network (ICON); at medical colleges, clinical research institutes, and public health institutes; and for pharmaceutical companies.

Some of the topics that we have covered so far include:

● Introduction to medical writing
● Medical writing in India
● Medical writing as a career option
● Basic skills in medical writing
● Ethical issues in medical writing
● Using Google search more effectively
● Using PubMed search more effectively
● Referencing styles
● Referencing software
● Writing a scientific manuscript and getting it published
● Writing narrative review articles
● Writing case reports
● Health writing for the web
● Health writing for the public

We also provide customized training solutions to our clients. Write to us about your specific training requirements.