Hetero is a fully integrated, global player in the pharmaceutical industry for more than 30 years. With 15 API & Intermediates manufacturing sites, Hetero can meet all your small molecule synthesis needs. Dedicated R&D laboratories support process development and optimization from gram scale to commercial scale. With 11 FDF manufacturing sites, Hetero can produce a wide variety of dosage forms, including sterile and injectable. Hetero's manufacturing sites are regularly inspected by global authorities, including the US, EU, Japan, Brazil and China. Hetero has received EcoVadis Gold certifications for its manufacturing network.
Our CDMO business unit supports clients from preclinical through clinical trials to approval and launch. Cost optimization for established processes and lifecycle management is also an area of extensive experience within Hetero.
We have many years of cooperation with biotechs, mid-sized pharmaceutical companies and global big pharma players worldwide.
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