Join Our Program/Register
Register now to join the Medcomms June Cohort
This structured program is designed to help healthcare professionals, dentists, pharmacy graduates, researchers, and aspiring medical writers master the art of clear, impactful scientific communication. Over the span of 2 months, participants will engage in 6 interactive sessions that blend theory with practical application.
Key Details
-
Schedule: Every Thursday, 7:00 – 9:00 PM (IST)
-
Format: Live online sessions followed by recorded access
-
Recorded Access: Available for 90 days, enabling flexible, self-paced learning
-
Resources: Comprehensive reading material provided to all participants
-
Practical Component: Each participant will develop communication assets that will be published on Rxnews.in
-
Faculty: Ramesh Mylapilli, 23 years of experience in Medical Communications
Practical Training
Students will gain hands-on experience in developing key medico-marketing deliverables, including:
-
Patient Education Literature
-
HCP Blog Article with Visual Abstract
-
Detailing Aids, LBLs, and Newsletters
-
Infographics, EDM, and RTE
-
Case Reports, Meeting Reports, Slide Kits
-
Storyboard for AV presentations and MOA Videos
-
Product Monographs
What You’ll Gain
-
A strong foundation in medical writing principles and ethical communication
-
Hands-on experience in drafting medico-marketing deliverables, manuscripts, abstracts, and medical news pieces
-
Guidance on structuring scientific content for clarity, accuracy, and impact
-
Opportunities to publish your work, enhancing your professional credibility
Register now to join the Regulatory Writing June Cohort
This intensive program is designed to equip participants with the skills and knowledge required to prepare high-quality regulatory documents that meet global standards. Over the course of 6 weeks, learners will engage in 12 structured sessions that combine live instruction with practical training.
Key Details
-
Schedule: 10 sessions over 5 weeks, Tuesday and Friday, 7 to 9 PM (IST)
-
Format: Live online sessions followed by recorded access
-
Recorded Access: Available for flexible, self-paced review after each session
-
Resources: All participants will have free access to our Reading Room/Library
-
Faculty: Ms Saumya Gupta has extensive experience in training students in Regulatory Writing
Practical Training
Students will gain hands-on experience in developing essential regulatory documents, including:
-
Clinical Study Protocol (CSP)
-
Investigator’s Brochure (IB)
-
Common Technical Document (CTD) Modules 1–5
-
Informed Consent Form (ICF)
-
Clinical Study Report (CSR)
-
Patient Narrative
-
Periodic Safety Update Report (PSUR)
-
Development Safety Update Report (DSUR)
-
Risk Management Plan (RMP)
What You’ll Gain
-
A comprehensive understanding of regulatory writing requirements and best practices
-
Practical skills to draft, structure, and format key regulatory documents
-
Insights into global regulatory expectations and compliance standards
-
Confidence to contribute effectively to clinical research and regulatory submissions
Register now to get access to the Reading Room
Our Reading Rooms are thoughtfully designed to support continuous learning and skill-building in the fields of Medical Communications, Manuscript Writing, and Regulatory Writing. It serves as a specialized library where members can deepen their understanding and refine their expertise.
Key Features
-
Curated Libraries: Separate collections tailored to Medical Communications, Manuscripts, and Regulatory Writing.
-
Comprehensive Resources: Access to a wide variety of reading material, including guidelines, case studies, and best practices.
-
Skill Enhancement: Materials selected to help learners strengthen their writing, analytical, and regulatory knowledge.
-
Flexible Learning: Members can explore resources at their own pace, revisiting key concepts whenever needed.
-
Material is encrypted and can be accessed online by registered members.
Benefits for Members
-
Reinforce concepts taught during live and recorded sessions.
-
Gain exposure to diverse styles and formats of professional medical and regulatory writing.
-
Build confidence in applying knowledge to real-world projects and publications.
-
Stay updated with evolving standards and practices in the field
