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- Cost optimization
- Synthesis of intermediates
- Developing non-infringing processes for APIs
- Improvement of processes for existing products in order to achieve ICH guidelines
- Independent chemical synthesis rooms (US Class 100,000 conditions) with walk-in fume-cupboards.
- Separate area for development of Cytotoxic Products
- Containment facilities for synthesis of highly toxic and highly potent materials.
- Capable of preparing API's suitable for preclinical and toxicological testing.
- Scale-up of API manufacture to GMP standards for clinical use
- Capable of carrying out process validation to FDA standards
Dedicated analytical laboratory with state of art instrumentation to support development.
- Capaple of carrying out specialized reactions & operations requiring: Cryogenic reactor, autoclaves, loop reactors, falling film evaporators, agitated thin film evaporator, high pressures and ozone
- Hydrogenation
- Oxidation
- Reduction
- Sulphonation
- Nitration
- Halogenation
- Chloro-sulphonation
- Condensation
- Friedel kraft
- Benzoylation
- Amination
- Alkylation
- Grignard
- Di-azotization
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