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Clinical Research
Introduction
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
Commencement
Patient Recruitment
 
Our regulatory consulting group is experienced in the development of positioning strategies, integrated planning, management, preparation of dossiers and submission to regulatory authorities for smooth transition and conduct of clinical research in India. Our experts are experienced in effective and diplomatic liaison with regulatory bodies. We ensure fast turn-around on regulatory documents and represent/ support you in meetings with regulatory agencies, for scientific advice.

This includes

Review of protocol
Preparation and review of clinical trial applications/dossiers
Import licenses
Effective communication with regulatory authorities
Assistance with independent review board/ethics committee approval
 
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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