Formulations developed
recognized
Approved Dossiers
Molecules covered
Your End-to-End Formulation Partner
From concept to commercialization, Bharat Parenterals’ integrated team supports your product development journey across all phases
                    Pre-Formulation & Feasibility
API profiling, excipient compatibility, solubility enhancement
                    Formulation Development
Oral solids & liquids, injectables, pediatric forms, fixed-dose combos
                    Analytical & Stability
Method validation, ICH studies, impurity profiling
                    Scale-Up & Tech Transfer
BE-ready pilot batches, process validation, seamless site transfer
                    Regulatory Documentation
CTD/eCTD compilation, EU & ROW support
                    Pre-Formulation & Feasibility
API profiling, excipient compatibility, solubility enhancement
                    Formulation Development
Oral solids & liquids, injectables, pediatric forms, fixed-dose combos
                    Analytical & Stability
Method validation, ICH studies, impurity profiling
                    Scale-Up & Tech Transfer
BE-ready pilot batches, process validation, seamless site transfer
                    Regulatory Documentation
CTD/eCTD compilation, EU & ROW support
Therapeutic Categories We Specialize In
We’ve built formulation expertise across a wide range of therapeutic segments
Cardiovascular
CNS & Psychiatry
Gastroenterology
Anti-infectives & Antivirals
Respiratory
Pain Management
Antiretrovirals
Scientific Infrastructure that Supports Every Stage
Our F&D facility includes pilot-scale production lines and a full suite of analytical labs equipped with
HPLC, UPLC
FTIR
UV-Vis Spectrophotometers
Particle Size Analyser
AAS
Multi-jar Dissolution Apparatus
Oral Solids Equipment
Liquids Processing
Topicals & Injectables
What Makes Our F&D Team the Right Partner
- Strategic, milestone-driven development model
 - Accelerated speed-to-market through agile R&D pathways
 - Proven capability in complex dosage development
 - Seamless integration from lab scale to tech transfer
 - Regulatory expertise for global submission support