For more than 45 years, we have operated on the principle that a valued and respected reputation must not be taken for granted, but continuously nurtured and strengthened. It is a commitment to ourselves and to our clients.

To provide industry-leading expertise, cutting-edge strategy, reliable performance, and service tailored specifically to the needs of each our customers and suppliers.

Active Pharmaceutical Ingredients:

ESSCHEM, supplies and sources, an extensive range of Bulk Active Pharmaceutical Ingredients and Intermediates from cGMP and FDA approved manufacturers.

Additionally, our partner companies have many more products in development that can be made available to customers at an early development stage.

API Representation and Marketing:

ESSCHEM has helped many different leading Active Ingredient manufacturers gain access to world markets – most especially the hard to penetrate Indian and regulated markets.

ESSCHEM can provide manufacturing partners with first class sales and product representation, regulatory approval management and ongoing strategic marketing advice.

• Finished Dosage and In licensing / Out licensing Opportunities:

We specialize in licensing / out licensing projects on behalf of our extensive range of partners and principals worldwide. We have a vast range of finished products in various therapeutic segments available for licensing opportunities.

In addition to ESSCHEM’s traditional focus on supplying quality APIs, we are actively collaborating with a number of finished dosage from manufacturers. Through our partners and alliances, we can offer formulation Development and Contract (Custom) Manufacturing with complete regulatory support.

• Custom / Contract Manufacturing & Outsourcing Services:

ESSCHEM’s extensive experience in the synthesis of Active Pharmaceutical Ingredients (API) is coupled with the wide capability range of our partner manufacturing plants.

Through ESSCHEM’s Network we are able to ensure the seamless production transfer and/or scale-up of most existing processes to established US-FDA inspected, CGMP manufacturing sites. Ask us about production of R&D, clinical validation or commercial batch quantities.

•Regulatory Services:

ESSCHEM has a good experience with the various regulatory authorities and organization. We can help you form the best submission strategy and help you ‘fast-track’ your products to market. Ask us for any assistance required in this regards.

•New Product Development:

ESSCHEM can facilitate in all stages of API development. Ask ESSCHEM for help with opportunity identification and validation, process development, scale-up and commercialization.