aajadi ka amrit mahotsav
May I help you ?

EPR Authorization for Nuclear Medicine Equipment and accessories


Nuclear Medicine Equipment and accessories

EPR authorization is mandatory for


Nuclear Medicine Equipment and accessories


Category : EPR Authorization

EEE Code : MDW5

Specialized medical devices known as nuclear medicine accessories and equipment are used in the diagnosis and treatment of a wide range of medical illnesses, such as cancer, heart disease, and neurological disorders. The Indian Technical Standard MDW5 describes the manufacturing and quality requirements for these essential medical devices in India.

These standards give producers of nuclear medical equipment and accessories precise technical criteria, quality standards, safety precautions, and testing protocols to follow. Adhering to these guidelines can help manufacturers gain credibility with healthcare practitioners, as well as open doors for their products in the cutthroat medical equipment industry.

Note: Manufacturers of nuclear medicine accessories and equipment must first get an EPR Registration Certificate.

Specialized medical devices known as nuclear medicine accessories and equipment are used in the diagnosis and treatment of a wide range of medical illnesses, such as cancer, heart disease, and neurological disorders. The Indian Technical Standard MDW5 describes the manufacturing and quality requirements for these essential medical devices in India.

 

About Extended Producer Responsibility (EPR) Authorization for E-Waste

An essential program to handle the expanding problem of managing electronic trash, or "e-waste," is called EPRA, or Extended Producer's Responsibility Authorization. Securing EPR authorization from the State Pollution Control Boards (SPCBs) and receiving the EPR Registration Certificate from the Central Pollution Control Board (CPCB) are the two steps in the process of obtaining EPR authorization. With the help of EPRA, manufacturers and importers of electronic goods will take over management of e-waste from consumers and local governments. Electronics importers and manufacturers are obligated by EPRA to assume full responsibility for the whole lifecycle of their products, from manufacturing to disposal. Establishing and financing collection networks, recycling centers, and appropriate e-waste disposal techniques are all part of this. 

 

Required Documents for Extended Producer Responsibility (EPR) Authorization for E-Waste

  • Address Proof Documents
  • Product Information (including model numbers and production/import history)
  • Valid BIS License
  • CPCB Certification

For more detailed information, please click here.

 

Registration Process for Extended Producer Responsibility (EPR) Authorization for E-Waste

Step 1: Fill out the application form

Step 2: Attach all the required documents

For more detailed information, please click here

 

Why Choose Brand Liaison?

Brand Liaison offers valuable assistance in obtaining an EPR Registration Certificate for Nuclear Medicine Equipment and accessories, Our services include:

  • Expert guidance
  • Streamline process
  • Comprehensive support
  • Cost-effective solutions
  • Time efficient

For a more in-depth understanding of the documentation and procedures involved in obtaining EPR Registration, feel free to connect with our team of experts at +91-9250056788 or +91-8130856678.

Back
Free Consultation !
×

Get Free Consultation

connect with us