A Comprehensive Series on Clinical Research Writing: Part I — Protocol Writing

Session Agenda

A protocol acts as a road map for conducting clinical studies and is an important quality control tool. Therefore, a well-written and detailed protocol is essential to communicate the important elements of the research study to the investigators, federal regulatory agencies, and the Institutional Review Board (IRB). It elaborates on the essential part of a clinical trial such as its significance, methodology, how it is carried out, etc. Operational feasibility, compliance with ethical and regulatory guidelines, and generation of quality data are some other characteristics of a thorough research protocol.

Enago conducted a webinar in association with Clinixir which aimed to help researchers, medical practitioners, and health science professionals by providing important tips and necessary guidelines for developing a comprehensive standard research protocol. We also addressed some of the most frequently observed oversights and other mistakes while drafting a protocol.

Researchers will learn:

• Importance of research protocol
• What is a protocol review?
• Factors to consider before writing a protocol
• How to structure a research protocol
• Tips for writing a clinical trial protocol
• Common pitfalls to avoid
• Recommended guidelines and template

Who Should Attend this Session? 

• Early-stage researchers
• Medical researchers
• Health professionals
• Clinical Research Professionals
• Doctoral students
• Senior Researchers