Mission
To help bring safe, effective therapies to patients sooner by delivering clinical research and safety services of uncompromising quality.
About Ethimark
A Research Partner Built on Rigor, Safety and Partnership
We bring together clinical, regulatory, data and safety specialists under one roof to help sponsors bring safe, effective therapies to patients sooner.
Science first.
Patients always.
Our story
Do the Science Right, and Keep Patients at the Centre
Ethimark was founded by a team of clinicians, scientists and industry professionals who saw that sponsors needed a research partner that was both technically strong and genuinely responsive.
Since then, we have grown into a multi-disciplinary organization serving clients across multiple regions, while staying true to our original promise: do the science right, and keep patients at the centre.
- Clinical trials delivered
- 130+
- Sponsors served
- 40+
- Investigators in network
- 1,500+
Vision
To be the most trusted scientific partner for sponsors developing the treatments of tomorrow.
Our values
What Guides Every Decision
Integrity
We follow the data and the regulations, every time.
Patient First
Every decision is measured against its impact on patient safety.
Partnership
Your goals become our goals.
Agility
We adapt quickly to changing study needs.
Excellence
We hold ourselves to the highest scientific and quality standards.
Why sponsors choose us
Global Standards, Deep Regional Knowledge
Our teams combine global standards with deep regional knowledge, so your program benefits from efficient site access, cost advantages and consistent quality wherever it runs.
Therapeutic Depth
Hands-on experience in oncology and other complex indications where protocol design and site selection make the difference.
Safety & Risk Management Specialists
Proven systems for demanding pharmacovigilance needs, including risk minimization programs and complex periodic reports.
New Molecules, Biosimilars & Vaccines
Multi-centre trial experience across innovative and follow-on products, designed to shorten your path to market.
Global Regulatory Know-How
Submission strategy and compliance support for major health authorities including US FDA, EMA, MHRA, WHO and CDSCO.
Leadership team
The People Behind Our Programs
CE
Leader Name
Chief Executive Officer
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CO
Leader Name
Head of Clinical Operations
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PV
Leader Name
Head of Pharmacovigilance
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RQ
Leader Name
Head of Regulatory & Quality
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Global presence
Where We Work
Headquarters
Ahmedabad, Gujarat, India
Global safety coverage
Pharmacovigilance support across 112+ countries.
Regional offices
Add each regional office with its city and country.
Certifications & accreditations
Standards We Work To
- ISO 9001 quality management
- ICH-GCP trained teams
- GVP-aligned PV system
- DIA member
- ACRP member
- ISPE member
Let’s work together
Ready to Start Your Next Study?
Tell us about your program and our experts will get back to you with a tailored approach and proposal.