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1
Development of First to File (FTF) & Future Generics Molecules.
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2
Development and Scale-up of Cost effective Commercial Technology of existing API & Intermediates.
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3
Development of Paper Technology of CRAMs, API and it’s Intermediate along with lab demonstration and scale-up support.
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4
Synthesis & Characterization of pharmacopoeial / in-house working standard and Impurities.
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5
Regulatory Affairs Management and cGMP Support Services (Consultancy & Outsourcing).
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6
Evaluation and Control of Genotoxic Impurities in existing & upcoming API.
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7
Specializes in patent non-infringing technologies for Antibiotics, Antidiabetics, Anti-Cholesterol, Anti- psychotic and other therapeutic class of drugs.
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8
Development of Custom Synthesis, material generation up to Kilogram with Technical package.
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9
Other study: Development of desired polymorph/New polymorph, Particle size distribution (PSD) with technical data.
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10
Conducting stability studies.
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11
Analytical support and Regulatory filing support to our clients.