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Clinical Research
Clinical Operations and Project Management
Process at Mithas Labs
Regulatory Strategy and Consulting
Clinical Monitoring Team and Activities
Clinical Monitoring Services
Advisory Doctors Panel
Gastroenterology Team
Therapeutic Experience
Clinical Trial Supply Management
Patient Recruitment

You can rely on our experienced project leaders and multifunctional teams who will work proactively and creatively to ensure success of your clinical development program. Each project team is headed by a project leader who manages and coordinates the activities of a multi-functional team comprising of Clinical Research Associates (CRA), Clinical Trial Associates and regulatory professionals who are known to be experts in their domain.

Our Project leaders are truly accountable for all your project deliverables, implementation, tracking and resolving all project related issues. These leaders ensure proactive identification and resolution of potential issues to keep projects on time or ahead of schedule. They coordinate with the clinical monitoring team for site management, development of site visit schedules, report preparation and review.

Our CRA's have experience under various therapeutic areas and have gone through vigorous training programs. They work closely with the project leader to ensure comprehensive planning, communication plans and project activities are documented in detail.

Clinical Research
CDM – Data Management System for Clinical Research
PGDCR / MS in Clinical Research
LIMS - Laboratory Information Management Systems
Batch III PGDCR starting on 19th January 2009.
We have landed at our new CRO facility, for a sparkling start
Autoscribe UK has appointed Mithas Labs to further expand its network of business partners offering pre-sales and post-sales services for its successful LIMS, scientific and business software solutions and implementation across India.
Mithas Labs has chosen Oracle Clinical for CDM License.
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