Clone Drug Registration with ANVISA: Understand the Process
Clone Drug Registration with ANVISA: Understand the Process
Brazil’s Anvisa’s Medical Devices for In Vitro Diagnosis Regulation (RDC 830/2023) comes into force in June 2024
Anvisa’s RDC 830/2023 Regulating Medical Devices for In Vitro Diagnosis comes into force in June 2024
Ensuring the Thermal Integrity of Pharmaceutical Products in Brazil
Brazil’s Anvisa, legislation provides guidance on the qualification of the transportation of biological products in bulk in their primary and finished packaging.