Formulation Development
We provide fully integrated solutions for the end-to-end development of innovative dosage forms. Leveraging Quality by Design (QbD) principles, our multidisciplined team ensures that every formulation is commercially viable and stable.
- Pre-formulation R&D
- Complex Solid Orals
- Injectable Development
- Modified Release Tech
- Bioavailability Enhancement
- Scale-up & Tech Transfer
Advanced Analytical Services
Our USFDA-registered facility is equipped with state-of-the-art chromatographic and spectroscopic instruments. We provide data-driven certainty through high-precision impurity profiling and ICH-compliant stability management.
- HPLC / GC Validation
- Impurity Characterization
- Stability Management
- Bioanalytical Support
- Extractables & Leachables
- Method Development
CDMO Services
Etico acts as a bridge between development and commercial manufacturing. We specialize in high-entry-barrier products, including complex oncology and parenteral formulations in a regulatory-safe environment.
- Clinical Batch Mfg
- Tech Transfer Support
- Oncology Suite
- Commercial Supply
- Regulatory Submission
- Process Validation
Ready to Accelerate Your Pipeline?
Our technical team is ready to discuss your specific pharmaceutical R&D and manufacturing requirements.
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