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Services offered

Method Development of Finished /Semi finished /API
Method Validation of Finished /Semi finished /API
Impurity analysis of Finished product/Raw Material
Impurity method validation
Stability Sample Analysis
Comparative dissolution Profiling

Preclinical Trial
We coordinate to conduct animal trial as per OECD guidelines
Accute Toxicity
Chronic/Sub-Chronic Toxicity
Occular Toxicity

Clinical Trial
Clinical Trials are conducted andcoordinated into the following Phases at Accurate Lifesciences :
Phase I to Phase IV Clinical trial

• Investigator selection
• Site Selection
• Feasibility Analysis
• Clinical Study Synopsis
• Clinical Study Protocol and CRF Designing
• IRB and EC document preparation and submission
• Site Selection Visit preparation
• Maintaining Patient/Subject Database
• Source document templates Designing

Study Conduct
• Site initiation visit
• Project Management
• Review of CRF and source documents, between monitor visits
• Quality assurance
• Investigtional Product Accountability
• Sample Shipment
• Lab Services
• Monitoring
• Conduct of project in compliance with ICH-GCP guidelines by training staff
• Data Management, Preliminary Analysis and presentation

Post Study
• Statistical Analysis
• Query resolution
• Medical Writing
• Study material storage
• Site follow up