Clinical Trial Support
Title: Seamless Clinical Trial Management
Subtitle: Ethics Committees | Regulatory Approvals | Site Readiness
Introduction:
LegMed simplifies clinical trial processes for pharmaceutical companies and research institutions, ensuring compliance with ICMR and DCGI guidelines.
Our Offerings:
- Ethics Committee Formation
- Drafting SOPs, training members, and documentation for IEC/IRB approvals.
- Regulatory Submissions
- CT-XML filings for DCGI approvals.
- Liaison with CDSCO for fast-track clearances.
- Site Setup & Monitoring
- GCP-compliant trial site preparation.
- Patient recruitment strategies and data management.
Key Achievement:
Facilitated Phase III trials for a diabetes drug across 5 sites within 4 months.
“Accelerate your research with LegMed’s trial expertise.”
Call +91 9830727839 or email : connect.legmed@gmail.com
