EPR Authorization is mandatory for Laboratory Equipment for in Vitro Diagnosis and Accessories

Category: EPR Authorization

Product Code: MDW6

In vitro diagnostic devices are the laboratory equipment that is used to test the samples collected from the human body to identify diseases to start proper treatment for the same. The importers, manufacturers and producers are required to get the EPR Authorisation for in-vitro diagnostic laboratory equipment. The CPCB provides EPR Registration and implies the duty to fulfil annual EPR compliance on the e-waste generators. The producers of in vitro laboratory equipment need to recycle the waste as per their EPR target. It encourages a recycling culture among businesses and ensures safe and secure disposal of harmful substances that are often found in electrical and electronic equipment. EPR compliances are the way to achieve the target of circular economy and sustainable development.

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