Medical Writing Training
Scrypto Analytics offers comprehensive, practical training in all aspects of medical writing to healthcare students and professionals with real-world medical writing skills, hands-on training and live projects guided through experienced medical-scientific writers.
Module 1: Introduction
- Introduction to Medical Writing
- Need for Medical Writing
- Future of Medical Writing
- Scope and Key Challenges in Medical Writing
Module 2: Basics for Medical Writing
- Microsoft Word Handling
- Understanding of different types of References
- Endnote Use
Module 3: Database Handling and Clinical Studies
- Boolean Search for Database
- Pubmed Learning
- Overview of Clinical Studies
- Types of Clinical Studies
Module 4: Literature Analysis and Summarization
- Literature Review and Analysis
- Summarization of Articles and Documents
Module 5: Medical Content Writing
- Newsletters
- Disease Summary
- Medical and Healthcare Blogs
- Drug Monograph Writing
Module 6: Medico Marketing
- Microsoft Power Point
- Slides Preparation as per Industrial SOPs
- HCP & Patient Education Materials: Product & Disease Brochures, Posters and Templates Using Microsoft Power Point and Canva
Module 7: Quality Check and Proofreading for Documents
- Step-by-Step Quality Check (QC) Process for Documents
- Comments and Track Changes for QC Process
- Step-by-Step Proofreading Process for Documents
Module 8: Publication Writing
- Introduction to Publication Writing
- Need for Publication and Types of Publication
- Protocol Development for all types of Publication
- Publication Writing: Research Article, Review Article and Case Report
Module 9: Clinical Research and Clinical Trial Transparency (CTT)
- Introduction to Clinical Research, Clinical Trials and Clinical Research Glossary
- Introduction to ICH Guidelines for Clinical Research
- Clinical Trial Transparency and Plain Language Summary/Lay Summary
- Redaction: Protected Personal Data (PPD) and Confidential Commercial Information (CCI)
Module 10: Regulatory Medical Writing
- Overview of CTD modules
- INDA (Investigational New Drug Applications) and NDA (New Drug Application)
- Investigator’s Brochure and Clinical Trial Protocols
- Clinical Study Reports (CSR)
Module 11: Regulatory Safety Narratives
- Introduction to Pharmacovigilance
- Regulatory Communication for Pharmacovigilance
- ICSR Narration and CSR Narratives
- Aggregate Reports Overview: SUSAR, PSUR, and PADER
- CTD 2.5 Clinical Overview and Health Authority Response Document Preparation
Module 12: Additional Skills
- ATS Format Resume Building Tips
- Interview Preparation
- LinkedIn Profile Building
- Job Hunting Skills through Naukri and LinkedIn