UltraMed Employees Training for MDR in India

ULTRAMED has assigned a few of its quality assurance and documentation teams to take training for the MDR in India. The MDR refers to the Medical Device Regulation, a set of rules and standards established by the European Union to ensure the safety and efficacy of medical devices sold in the EU. This regulation replaced the previous Medical Device Directive (MDD) and imposes stricter requirements for the design, manufacturing, and marketing of medical devices. To comply with the MDR, medical device companies need to ensure that their products meet the new regulatory requirements, as well as ensure ongoing compliance.