What We Do · Formulation R&D
Formulation R&D & Troubleshooting
What We Do · Formulation R&D
Formulation R&D & Troubleshooting
Our formulation development service builds scientifically sound, stable and regulatory-ready products — and resolves the most challenging problems faced during development and manufacturing.
We support oral solid, semi-solid, injectable, ophthalmic and oral liquid dosage forms with an integrated approach to formulation, process and analytics.
Core Capabilities
Integrated services delivered with scientific rigor
01
Pre-formulation & Compatibility
- API characterization, solubility and polymorphism studies
- Drug–excipient compatibility studies
- Selection and optimization of excipients
- Packaging material selection and compatibility studies
02
Formulation Development
- Prototype formulation development
- Process development (granulation, blending, compression, coating)
- Development of oral, semi-solid, injectable and ophthalmic formulations
- Scale-up and pilot batch manufacturing
03
Equipment & Capabilities
- Rapid Mixer Granulator (RMG) and Fluid Bed Dryer (FBD)
- Tablet compression machines and coating pan / auto-coater
- High-shear mixers and homogenizers
- ICH-compliant stability chambers
Typical Timeline
How a typical engagement unfolds
01
Pre-formulation & compatibility
2–6 weeks
02
Formulation development
4–12 weeks
03
Analytical method development
3–6 weeks
04
Method validation
2–4 weeks
05
Stability studies (initial)
6–12 weeks
06
Scale-up & pilot batches
4–10 weeks
Overall R&D duration: approximately 3–9 months, depending on product complexity.
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From early development through commercialization — backed by science, quality, and regulatory expertise.
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