A. Preformulation Studies
- Extract selection
- Dosage definition
- Selection of mixing solvents and excipients to optimize stability and efficacy
B. Formulation Development Process Validation
- Method development and validation to meet the most
demanding industry and regulatory requirements
C. Stability Studies
- Stability studies of raw material and finished products
- Real time and accelerated analysis
- Analytical testing of related substances and quantification of active content in formulations
- Meets ICH guidelines
D. Scale-up Clinical Trial Samples and Pilot Batches for
- Capsules
- Creams, gels, lotions and liniments
- Oral syrups
- Powders and granules
- Medicinal teas and lozenges
E. Technical Support for Preparation of
- Technical Dossiers
- Drug Master Files
- Standard Operating Procedures