Consultation Overview
Ethics (IEC) Submission Documentation
Qualified Doctor with experience in developing comprehensive, compliant, and well-structured submissions for Institutional Ethics Committee (IEC) and Institutional Review Boards (IRB). Skilled in drafting key documents including research protocols, informed consent forms, patient information sheets, case report forms, and regulatory checklists in accordance with ICMR, ICH-GCP, and international ethical guidelines. Adept at ensuring accuracy, completeness, and ethical compliance while streamlining the approval process.
Service Details
What's Included
- Video consultation
- Personalized guidance and advice
- Session notes and recommendations
- Follow-up support via email
Pricing Options
- Single Session ₹300
- Full Project ₹4,000
About Cynthia Leslie
Clinical Research Professional with hands-on experience in executing randomized controlled trials, biomarker research, clinical data management, ethics documentation, data analysis, and manuscript drafting. Experienced in ethics submissions (IEC), CTRI registration, clinical data management, biological sample processing, data interpretation, and manuscript preparation for indexed journals.
Experience
Scientific Writing
Specialized expertise in scientific writing with 1 years of professional experience.