Formulation Development
- Oral solid dosage – Tablets and capsules – Immediate, ODT, Sublingual, Delayed, Extended, Sustain Release utilizing dry and wet granulation, matrix, multi-particulate, MUPS etc.
- Liquid Dosage – Oral solutions, syrup and suspensions.
- IP Evaluation
- Pre-formulation and Feasibility studies
- API evaluation
- Prototype development and testing
- Design of Experiments
- Quality by Design
- Process Optimization Studies
- Bio Studies Management
Analytical Development
Analytical methods developed using state of the art laboratory equipment adhere to the highest quality standards and regulatory compliance
- Analytical Method development and validation
- Particle size analysis
- Dissolution and drug release profiling