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600+ Different Tests
Experienced professionals
We’re Responsible for The Safety of Cosmetics Testing
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Experienced professionals
We’re Responsible for The Safety of Cosmetics Testing
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About Research
Reliable Agroscience & Soil Analysis Research.
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Medical Research
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Blood Resources
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Laboratory Services
Reliable & High-Quality
Laboratory Service
PATIENT CENTRIC BE STUDIES
For certain classes of drugs like cytotoxic and psychotropic drugs, BE studies can be done only on appropriate patients.
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These studies will be executed at hospital sites and centrally controlled by Mahindra City Amaris Clinical Facility
BA/BE STUDIES IN HEALTHY VOLUNTEERS
Amaris can undertake the following Bioavailability/Bioequivalence studies
- Single & multiple-dose studies
- Fasting & Fed studies
- PD studies
- Cross over and parallel studies
- Replicate studies
- Proof of concept studies
- Special population studies (postmenopausal and geriatric studies)
- Topical transdermal patch studies
- Inhalational studies
- Injectable studies
CLINICAL ENDPOINT STUDIES
An endpoint is the outcome that researcher’s measure during a clinical trial in order to determine whether or not an experimental therapy is effective. Researchers select endpoints based on clinical trial design, the nature of the condition being treated, and the anticipated effect of the drug being tested. In some cases of generic drugs, the bioavailability cannot be demonstrated using conventional PK/PD studies.
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Hence a clinical end point is determined to demonstrate the equivalence to the innovator product. A clinical endpoint is an outcome that represents direct clinical benefit, such as survival, decreased pain, or the absence of disease.
CLINICAL TRIALS PHASE II TO PHASE IV CLINICAL TRIALS FOR IND/NCE
No matter what stage of Clinical Trials you are, we can help you. Amaris with the help of elaborate Investigator network across various therapeutic segments, experienced and insightful Project Management Team, established mechanisms for Site Management, Clinical Data Management, Clinical Trial Management, Medical Writing, Quality Assurance service, Training and Regulatory Liaison activities can provide effective Clinical Trial services to its clients. With a strong investigator network across the globe, Amaris Clinical is forging ahead as a reliable service provider in this segment. We provide the following expert service for drug development process:
- Selection of sites & regulatory assessment
- Clinical Operations
- Regulatory Affair
- Project Management
- Protocol Writing
- Supervision of Protocol Deviations
- Biostatistics
- SAS Programming
- Risk-Based Monitoring & Interim Monitoring
- Pharmacovigilance
- Medical Services
Molecular Testing
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- The Mycobacteriology Section
- The Aerobic Bacteriology Section
Why Choose
Well Ensure You Always Get The Best Results.
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Medical Research
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Blood Resources Program
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Extramural Funding
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OUR EVENTS
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What Our Patient Say?
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