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Taking care of your Clinical and Bioanalytical Research

CLINICAL RESEARCH

Phase -I to Phase -IV clinical trials

Clinical trials for medical devices

BIOANALYTICAL SERVICES

Providing best solutions for your bioanalytical needs in BA-BE and Invitro studies

PROJECT MANAGEMENT AND REGULATORY SERVICES

Manage your projects with defined timelines and budget with CTQ and QBD approach

All regulatory solutions for all major regulatory submissions 

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Phase-I to IV clinical trials

Observational studies

Bioequivalence And Bioavailability studies

Medical Devices Trials

Site engagement 

GLP Training

Site Initiation, Monitoring And Closeout

Pharma value chain

Clinical Data Services

Medical writing-ICF, Protocol, Reports

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Bioanalytical support for all complex molecules

Bioanalytical monitoring And data review

Invitro release test

Invitro permeability test

Kinetic binding studies

Biowaiver studies

Project management with QBD and Risk management approach 

Regulatory services for all major regulatory bodies including US FDA, EMA, WHO, ANVISA, NMPA China, DCGI India, NPRA Malaysia, MOH Turkey, IFPMA Africa, SAHPRA South Africa

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