Pharmaceutical Development Services
We offer pharmaceutical development services for oral solids, liquids, creams, ointment and sterile injectable from our facilities in US, UK and India. As a leader in integrated solutions, we seamlessly engage our global sites to conduct development work in parallel; accelerating time to market and reduce costs for our customers.
Pharmaceutical Development Capabilities
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Phase I to III clinical development (NCEs)
- Oral Solids
- Sterile Injectables
- Liquid filled Capsules
- Creams and Ointments
- Powder-in-bottle to Drug-in-Capsules
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Formulation Development in various dosage Forms
- Oral Solids
- Conventional oral solid forms
- Oral disintegrating tablets
- Sublingual tablets
- Press coated tablets (Sub coated tablets)
- Bi-layered, Delayed release, Modified release
- Granules for reconstitution
- Sterile Formulations
- Sterile Liquids – Injectable & Ophthalmic
- Lyophilized products
- In-situ salt formations
- Non-aqueous formulations for liquid
- Nanoparticles and Liposomes
- Creams and Ointments
- Oral Solids
- Paediatric formulations
- Hormonal formulations (Oral contraceptive pills)
- Controlled drug substances
- Oncology drug products (Sterile and Solid Dosages)
Key Features of Pharmaceutical Development
- Supports development to clinical manufacturing (50 g to 35 kg)
- Blinding by over-encapsulation
- Capability to handle low RH compounds handling (<30%)
- High-potency compounds (OEL: 1 µg/m3)
- Design of experiments using Statistica software
- Multi-particulates (GPCG 2 and 30)
- Explosion-proof area for handling non-aqueous Solvents
- Manufacturing suites for liquids, creams and ointment production
- Specialized IPQC tools such as Geopyc, Shulze Ring-shear tester for powder / compacts evaluation, sifting & fluidization type Segregation Testers