• Fasted / Fed Conditions
• Immediate / Modified-release Preparations
• Interaction Studies
• Various Routes of Administration
• Healthy Volunteers / Special Population

With a continuously updated list, our analytical laboratory offers highly selective and sensitive validated methods for assay of drugs / metabolites and endogenous compounds from biological matrices using LCUV, LCFL, LCECD and LC-MS/MS-6 techniques, Pharmacokinetic & statistical data evaluations, reporting of study results and archiving of all study related data.

We use variety of approaches including Fluorescence HPLC Detection, Electrochemical Detection and Triple Quadruple Mass Spectrometry. Our expertise in Rapid Method Development and Validation allows us to offer timely and cost-effective analysis of samples.

Clinical Project Management
A Project manager leads a team of Clinical Research Associates (CRAs), Data Managers, Safety Monitors and Quality Assurance Auditors. The Project Management Team takes care of:

• Investigational sites & Investigators: Selection, Initiation & Monitoring Visits
• Protocol Planning & Development
• Presentation of Protocol at Investigators Meeting
• Designing of Case Record Forms (CRFs), Informed Consent Forms (ICFs), Investigator Manuals and other documents
• Documentation
• Investigational Materials Management
• Investigators’ & Staff Training on GCP Guidelines
• Source Data Verification at sites
• Safety Management including Adverse events / Serious adverse events
• Handling QA Audit Visits
• Close Out Visits

Herbal Analysis
We have developed competency in screening herbal medicines for their content & quality. We help the client in choosing right raw material and/or extract from cultivation stage through harvesting to marketing.