The company has several years of experience in developing and supplying generic products to regulated markets.

Our in-house R&D is capable of developing, transferring technology to manufacturing facilities, and providing continuous support to our partners including Regulatory Affairs to augment our partners’ marketing footprint. Quality Assurance is an integral and critical part. Non- conflicting and compliant audits for Active Ingredient Manufacturers, Finished formulation manufacturers and BA/ BE Study centres including monitoring studies are conducted and acceptable by European Qualified Persons.

With several manufacturing partners accredited with EU GMP / USFDA status, we offer seamless service from the development of the product to the support of the product. Facilities to manufacture most of the dosage forms are available.

It is our strong belief that in a dynamic and highly regulated pharmaceutical market, our partners are fully engaged in the expansion of their footprint. We supply the product and ensure there is consistency in supply.

Our business strategy is based on the principles of high ethical standards. We aim to achieve our partners’ growth goals along with ours. Long-term collaboration with companies adhering to similar values and high ethical standards is sought. Business models are flexible and innovative to cater for customers and evolved based on the merits of every opportunity – in licensing, co-development, contract manufacturing and supply.

We provide our partners with international standard quality products at competitive prices.

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Our business development team is easily accessible for our partners