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Expanding Our Vision Globally image

Expanding Our Vision Globally

Cadila undertakes contract manufacturing to offer partners a win-win working relationship, under a strong strategic alliance. Over the years, the company has carved a distinguished niche for itself in the global regulated market, where we constantly aspire to:

  • Grow through strategic territory expansions, partnerships, globalization for deeper penetration into evolving markets, through joint ventures and subsidiaries.
  • Develop a broad portfolio of products through non-infringing processes to emerge as a significant player in the generics market.
  • Emerge as a market leader in the manufacture and supply of premium quality, innovative specialty, generic formulations.

If you are looking to grow with us, we assure you of the following:

  • Contract manufacturing in all dosage forms.
  • End-to-end service in terms of raw material purchase, production, packaging and quality control.
  • We are extremely flexible in meeting our clients’ demands and are able to perfectly integrate with your existing supply chain framework.

Under this umbrella of service we offer:

  • APIs inspected and approved by the USFDA for Fluoxetine and Ethambutol.
  • US DMF / EDMF / COS filed / under process for about 20 products.
  • ISO 9002 / ISO 14000 certified bulk actives manufacturing facility, offering facilities for “Contract Manufacturing”.
  • Anti-allergic, Cardiovascular, Anti-diabetic, Disinfectants.
  • CNS, NSAIDs, Anti-TB, Gastrointestinal, Anti-histamines.

Under this umbrella of service we offer:

  • State-of-the-art facilities, conforming to the stringent specifications of cGMP, TGA-Australia, and MCC-South Africa.
  • The annual production capacity of 3,900 million tablets, 150 million capsules, 6,000 - kilo litres liquid dosages, and 168 million vials and ampoules.
  • Capability to produce dosage forms in sterile and non-sterile formats in all therapeutic categories, including lyophilization facility.
  • Sterilized, dedicated world-class facilities for the production of Beta-Lactam, Cephalosporin, Rifampicin, and Insulin.
  • The board-certified and experienced technical team, specializing in all areas of drug manufacturing, including quality control, quality assurance, research and development for all range of products.
  • Experienced professionals and highly-qualified management staff, with SAP ERP and Supply Chain Management on board.
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Why Align With Us?

There are several good reasons, a few of which are enumerated below:

  • We promise a reliable, continuous supply of quality products – validated and approved by competent authorities with their registration files.
  • You would have to make a minimal investment in capital-intensive facilities.
  • You will gain in terms of net earnings and improved cash flow.
  • By outsourcing your manufacturing to us, you can divert your resources to your core competencies, say R&D and marketing.
  • Before dispatch, all products are finally vetted by our quality control team.
  • For us, deadlines are sacrosanct. WE strictly adhere to the committed timeliness.
  • We guarantee complete customer satisfaction with our deliveries.
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