As a Global Indian Full-Service CRO, Ethicare supports Global and Local Patient Based Trials of all types and phases for the Pharmaceutical, Biotechnology, Nutraceutical and Medical Device Industries. Our services include end to end Study Planning and its mindful Management along with Quality Compliance. Customer service is our core value along with our commitment to delivering new therapies to patients.
To establish ourselves as a comprehensive drug development partner to our clients by offering Clinical Research Solutions of the highest standards.
To enhance quality by keeping pace with latest techniques and procedures, ensuring scientific validity of all research projects and complying with global regulations.
We aim be the preferred and trusted clinical development partner for global Pharmaceutical, Biotechnology, Nutraceutical and Medical Device companies.
To shape the future of the clinical research industry by ensuring (superior) quality, reliability and value-added services.
Committed to advancing science, we foster strong partnerships to drive meaningful breakthroughs.
• 1st Domestic CT
• Pharmacovigilance started
• 35 CT Conducted
• BMGF Funded Project in India & Africa
• Ethicare EDC Platform Created
• Global Projects for USA, EU, UK, LATAM etc.
• 125 CT Conducted
• Global Projects for USA, EU, UK, LATAM, Australia, etc.
• 240 CT Conducted
At Ethicare, we are committed to fostering trust, transparency, and collaboration with our partners and clients. Thank you for choosing us as your trusted partner in clinical development
Protocol Feasibility, Site Selection, Vendor coordination, Drug Supply Coordination, Grant Negotiations, owns all plans with program management, TMF development etc.
Cloud Based EDC, eCRF Design, 21CFR part 11 Compliant, Database Build up & Validation, Data Entry, Edit Checks, DCF, Database Lock
Providing the highest quality of monitoring including Medical Monitoring, in concert with ongoing Ethicare studies or as a stand alone service
Protocol input with regard to development scenarios, SAP development, interim and final analysis, population breakouts etc. (Note: outsourced service)
Clinical Trials and Post Marketing Safety Services Like, PSMF, Literature, ICSR, Aggregate Reports, Signal, RMP, SDEA, MIS, etc.
Study Protocols, CSR, IB, ICF,
Patient diaries, Patient safety
narratives, Manuscripts &
Scientific abstracts, Regulatory
Modules
Proficient across diverse therapeutic fields , Small molecule and biologic experience , Large service suite , Flexible business partner
Rigorous SOPs designed , Executive oversight on every project , Single point of contact and commitment to quality
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis, pulvinar dapibus leo.
Global Client Database ,Dedicated feasibility and clinical science team, Experience with health authority requirements globally , Consistently passing inspections with global health authorities (USFDA, Health Canada, EMA MHRA, WHO, TGA, CDSCO, CIS etc.)
As a Global Indian Full-Service CRO, Ethicare supports Global and Local Patient Based Trials of all types and phases for the Pharmaceutical, Biotechnology, Nutraceutical and Medical Device Industries.
Copyright © 2025. Ethicare-cro.com. All rights reserved. Developed by SM Infosoft Pvt. Ltd.
