Transforming Molecules into Medicines
At the heart of drug innovation lies our Formulation Development Department, where science meets precision to create safe, effective, and patient-centric pharmaceutical products. Our team of experienced scientists and formulation experts is dedicated to developing high-quality dosage forms tailored to meet therapeutic goals, regulatory standards, and market needs.
The projects handled in past with product development of therapeutic agents from category including Antimuscarinics, Expectorant and Antitussive, Alpha-1 Blocker, Antihistamine, Antidepressant, NSAIDs, Antidiabetic, Anti-Hypertensive, Antibiotic.
Further product development projects include drugs from therapeutic category including Anti-Hypertensive, Antibiotics, Anticonvulsants, Anticholinergic, Alpha-1 Blocker, Phosphate Binder, Mucosal Protectant, Antibacterial etc.
What We Do
We specialize in the formulation development of a wide range of dosage forms, including:
- Oral Solids: Tablets, capsules, powders, granules
- Oral Liquids: Syrups, suspensions, solutions
- Topicals: Creams, gels, ointments, lotions
- Novel Drug Delivery Systems: Sustained release, controlled release, nano-formulations
Our development process includes:
- Pre-formulation Studies:
Characterization of active pharmaceutical ingredients (API), including solubility, stability, and compatibility testing. - Formulation Design and Optimization:
Selection of excipients and process parameters to achieve targeted performance and bioavailability. - Scale-Up and Technology Transfer:
Seamless transition from lab-scale to pilot and commercial manufacturing. - Stability Studies:
In-house evaluation of formulation performance through dissolution, disintegration, and accelerated stability testing.
Our Capabilities
- State-of-the-art R&D laboratories with modern formulation and equipment
- Expertise in regulatory documentation and support for global filings (ANDA, CTD formats)
- Collaboration with development, quality assurance, and manufacturing units for end-to-end product development
- Team: We are team of skilled and experienced scientists in area of and pharmaceutical product development with qualifications M.Sc., M. Pharm., and Ph.D.
Why Choose Us?
- Proven track record in developing complex formulations
- Rapid prototyping and agile development processes
- Strong focus on innovation and continuous improvement
- Committed to patient safety, compliance, and therapeutic excellence
Formulation Development Department
Preformulation
- Polymorph screening & selection
- Salt form selection
- Crystalline properties
- pH solubility & stability
- Solid-state & solution-state stability
- Photostability
- pKa & partition coefficient
- Hygroscopicity & solubility studies
- Excipient compatibility
- Leachables & extractables
- Flowability & particle size
- Container–API interactions
- Intrinsic dissolution
Formulation Development
- Tablets: Immediate, Sustained, Delayed, Film-coated, Layered
- Pellets: Tablet or capsule filled
- Powders: Bottles, sachets, capsules
- Liquids: Solutions, suspensions, syrups, emulsions
- Semi-solids: Creams, ointments, gels, lotions
Capabilities
- Direct compression
- Dry granulation
- Roller compaction
- Wet granulation
- Fluid bed granulation
- MUPS
- Tablet compression
- Unit Dose Packing
Analytical Research and Development
Our experienced scientist work in tandem for the success of development projects. The following are core subdivision of departmental activity include:
- Method development by QBD
- Method validation as per ICH, US, MHR etc
- Method transfer
- Method qualification
- Elemental impurities risk assessment
- Nitrosamine impurities risk assessment
- Cleaning Method Development/Validation (Rinse & Swab)
- Stability studies including zone IV studies
- Chiral analysis
- Solubility studies
- Intrinsic dissolution
- Multimedia dissolution profiling
- pKa and partition coefficient determination
- pH solubility and stability
- Solid state, solution state & photo stability
- Capability /Instruments
Our AR&D lab features HPLC-PDA, HPLC - UV, Atomic Absorption Spectroscopy, Gas Chromatography, dissolution testers, UV-Vis, and stability chambers (Zone I–IVb) to ensure drug quality, and others meeting global regulatory compliance.