Navigating Complexity with Confidence.
What We Do
Here we Streamline approvals and submissions for clinical research in Bangladesh and beyond. We offer Expert guidance in Clinical trial application preparation, Ethics committee submissions, Regulatory agency liaison and post-approval support
Our Expertise
– In-depth DGDA knowledge avoids delays
– Local representation & advocacy for global sponsors
– Proactive updates on regulatory changes
– Liaison with local regulatory authority (DGDA) and ethics committees.
– Submission preparation, application filings, amendments, renewals.
– Regulatory strategy, ensuring alignment with local and international standards.
Client Journey
1. Regulatory Strategy
2. Document Preparation
3. Submission & Follow-Up
4. Compliance Maintenance
Why Work with Us
– We know the DGDA and IRB landscape in Bangladesh well.
– Helps avoid wasted time, rejected applications, and unexpected regulatory hurdles.
– Sponsor can focus on clinical execution while we manage the red tape.
– Our Regulatory intelligence will keep you aware of rule or guideline changes.
– Local representation & advocacy.
Contact With Us
Start your regulatory submission with AMZ CRO.