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.

Business Opportunities and Strategic Alliances

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.

Active Pharmaceutical Ingredients (APIs)

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.

Generic Formulations

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.

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.