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In January 2023, the company had announced the successful completion of the full set of clinical studies of its proposed rituximab biosimilar candidate DRL RI, with the intention to file in the United States, European Union and other regionsFollowing dossier submission in April 2023, the regulatory agencies have now.

Andhra pradeshUnited kingdomUnited statesJayanth sridharFresenius kabiEuropean medicines agencyExchange commissionDrug administrationReddy laboratories ltdRegulatory agencyEuropean unionGood health cant waitBiologics license applicationGlobal headLow tumour burden follicularGood health cant wait