- • API characterization & compatibility studies
- • Solid oral dosage forms (tablets, capsules, granules)
- • Modified-release and immediate-release formulations
- • Prototype development & optimization
- • Method development & validation as per ICH guidelines
- • Stability-indicating methods
- • Impurity profiling and characterization
- • QC support & analytical troubleshooting
- • Deliver affordable and high-quality medicines.ICH stability studies (Zone II to Zone IVb)
- • Photostability and stress testing
- • Real-time and accelerated studies
- • Complete stability protocols and reporting
- • Product development reports (PDRs)
- • Technical data packages & scientific justifications
- • Batch scale-up and process optimization
- • Technology transfer to manufacturing sites
- • Tech packages with MFCs, BMRs, and process validations
- • Support for Exhibit and Commercial batches
- • Client-driven research projects
- • Troubleshooting and formulation problem solving
- • Generic product development
- • Lifecycle management and line extensions
Our work is applicable with wide variety of distributions.
Industries We Serve
