Regulatory Affairs
Registration and lifecycle support for medical devices, IVD, medicines, cosmetics, APIs and pharmacovigilance.
Explore practice →About Ziva DRA
Local regulatory depth.Global business perspective.
Ziva DRA helps healthcare, pharmaceutical and life-science organizations navigate regulatory affairs, research, market access and business compliance in Bangladesh.
Who we are
A Bangladesh-focused regulatory and market-access partner.
Supporting regulated healthcare and life-science businesses through connected market-entry and compliance pathways.
Ziva DRA helps healthcare, pharmaceutical and life-science organizations navigate regulatory, research, compliance and market-access requirements associated with Bangladesh.
Our work spans medical devices, IVD, medicines, API source validation, pharmacovigilance, clinical and research support, dossier activities, GMP consulting and business compliance.
By bringing these capabilities together, we support both individual regulatory assignments and broader market-entry programs involving multiple connected workstreams.
Bangladesh FocusLocal regulatory and commercial context.
Healthcare SpecializationSupport for highly regulated sectors.
Integrated DeliveryRegulatory, research and compliance workstreams.
International PerspectiveStructured support for overseas companies.
What we do
Four practices. One market-access lifecycle.
Connected specialist capabilities allow projects to move from requirement assessment into practical execution.
Clinical & Research
Support for clinical trial activities, BA/BE studies and bioanalytical requirements.
Explore practice →Global Market Access
International regulatory affairs, dossier preparation and GMP consulting.
Explore practice →Business Compliance
Company formation, licensing, Tax & VAT, IRC, ERC and trademark support.
Explore practice →How we work
A structured engagement model.
A clear operating rhythm keeps complex regulatory and compliance programs manageable.
Consultation
Understand the product, business and market objective.
Assessment
Identify regulatory, research and compliance requirements.
Preparation
Organize documentation and required submissions.
Execution
Coordinate submissions, studies and compliance processes.
Ongoing Support
Manage follow-up, renewals and continuing obligations.
Discover Ziva DRA
Learn more about the company.
Why Ziva DRA
Explore the principles and capabilities behind our regulatory and market-access approach.
Discover why →Our Team
Meet the people supporting regulatory, research and compliance work.
Meet the team →Contact Us
Discuss a regulatory, compliance or market-entry requirement.
Contact Ziva DRA →Planning a regulatory or market-entry project?
Tell us about your product, company or Bangladesh market objective.