We undertake projects for the development of “Generic Formulation Products” for the following regulatory and non-regulatory markets-

• Regulatory markets (US, EU, JAPAN, etc.)
• Non-regulatory (WHO, RoW, Asia, CIS countries, etc.) markets.

For simple and complex Generics like-

Solid oral dosage forms (Tablets, Capsules, Oral Liquids and Suspensions, etc)

• Immediate release tablets and capsules
• Enteric coated tablets
• Enteric coated granules in capsules
• Sustained (Modified) release tablets
• Orally Disintegrating (and Sublingual) tablets
• Effervescent tablets
• Sugar Coated tablets
• Dry Powder for suspension

Injectable sterile dosage forms (all variants)

• Liquid injectables
• Powder for solution injectables
• Powder for suspension injectables
• Modified release injectables
• Prefilled Syringe type injectables

Ophthalmic sterile dosage forms (all variants)

• Ophthalmic solutions
• Ophthalmic suspensions
• Ophthalmic ointments

Transdermal dosage forms (all variants)

• Transdermal ointments
• Transdermal Gels

We provide end to end solution that is from prototype development to regulatory approval and transfer to commercial facility for successful commercialization.