We have ensured world-class quality in design, equipment and operations in all our manufacturing facilities across the world. We have over 40 ( API & finished dose) state-of-the-art manufacturing sites spanning 2 continents. These manufacturing units are located in India, Finland, Hungary, Romania, Ireland. Our units ensure that we are able to provide best-in-class products to patients across the globe.

Our manufacturing operations are focused on producing generics, branded generics, speciality, over-the-counter (OTC) products, anti-retrovirals (ARVs), Active Pharmaceutical Ingredients (APIs) and intermediates in the full range of dosage forms, including tablets, capsules, injectables, ointments, creams and liquids. We also manufacture speciality APIs, including controlled substances, steroids, peptides and anti-cancers.

We have a highly skilled team of regulatory affairs specialists who are well versed with regulatory policies and procedures around the world. They have a wealth of experience in the timely filing of dossiers as well as handling regulatory queries from both authorities and customers.

A wide range of regulatory agencies routinely conduct stringent audits of our manufacturing facilities for compliance with Current Good Manufacturing Practices (cGMP). Several regulatory agencies, including FDA-USA, EMA-Europe, MHRA-UK, MCC-South Africa, TGA-Australia, ANVISA-Brazil, WHO-Geneva, BfArM-Germany, KFDA-Korea and PMDA-Japan, have inspected our facilities.