Formulation Development
At Prim Drugs & Pharmaceuticals (I) Pvt Ltd, we recognize the importance of our clients’ requirement to develop robust and compliance formulations.
Our strong scientific team has a broad range of expertise and experience in collaborative practices with a global customer base for formulation development and analytical support
We also provide extensive pre-formulation studies, toxicology formulation, formulation development, analytical method development and validation, manufacturing process scale up, stability studies as per ICH guidelines and manufacturing of clinical batches under cGMP environment.
Our Formulation development Process is as follows
- Feasibility Studies
- Reference Listed Drug(“RLD”) Reverse Engineering
- Excipient Compatibility Studies
- Formulation Development
- Formulation Optimization
Clinical and commercial formulations
- Tablet (immediate / modified / sustained / extended release)
- Semi-solid: Creams,gels,ointments,pastes,lotions
- Capsule (immediate/modified)
- Non-sterile solution/suspension/syrups
- Powder-in-bottle
Formulation Development Capabilities
- Clinical and commercial formulations
- Excipient compatibility
- Solid, semi-solid and liquid formulations
- Highly potent compounds in oral liquid and semi-solid dose formats
- Delayed or modified release formulations, including enteric coated formulations
- Modified/sustained release formulations
- Low/high drug load
- Orally disintegrating tablets(fast dissolve)
- Pediatric dosing