Design, execute and monitor of product development strategies
Literature Search & Technical Patent Review
Pre-Formulation Development
Drug-Excipient Compatibility Studies
Formulation & Process Development & Optimization
Scale-Up & Technology Transfer
Process Validation Studies
Packaging Development Studies
Review and evaluate development data
Analytical Method & Specification development
Content Uniformity, Related Substances, Dissolution etc.
Content Uniformity, Related Substances, Dissolution etc.
Forced Degradation Studies
Method & Site Transfers
ICH Stability Studies & Stability Sample Analysis
Risk based decision making and execution framework
CTD Filings
Dossiers Meeting Various Global Requirements
IND/NDA & ANDA Support Documentation
Licensing
Collaboration with allied fields
Facilitate selection of actives, critical Excipient, make a use of novel Excipient, and packing components.
Finding a suitable site for development manufacturing
Quality Auditing
Quality Services
Sourcing Services