Industry

EPR Registration (E-waste)

Get professional support for obtaining EPR registration for medical device and IVD importers, manufacturers and brand owners under the E-Waste Management Rules, 2022.

Overview

The Extended Producer Responsibility (EPR) registration is mandatory for medical device and IVD importers, manufacturers, and Brand Owners of Electrical and Electronic Equipment (EEE) i.e. products that are dependent on electric current or electro-magnetic field in order to become functional. E-waste EPR registration is granted by the Central Pollution Control Board (CPCB).

Services

We provide end-to-end services for obtaining EPR registration under the E-Waste Management Rules, 2022 for importers, brand owners and manufacturers which includes:   

  • EPR application filing
  • EPR application review
  • EPR action plan preparation or review
  • EPR portal account creation
  • EPR application rejection support
  • EPR application query support
  • EPR compliance support
  • EPR registration amendment
  • EPR registration renewal
  • Login credentials change support
  • Authorized person change support
  • EPR show-cause notice support
  • Representation before CPCB
  • Medical devices
  • IVD
  • Spare parts
  • Components
  • Consumables
  • Accessories
  • EPR Registration
  • Importer Registration
  • Brand owner registration
  • Producer registration
  • Manufacturer registration
  • EPR registration number
  • Custom clearance EPR
  • EPR Compliance
  • EPR Certificate
  • E-waste
  • Electrical and electronic equipment
  • EEE
  • Used EEE
  • Manufacturer
  • Producer
  • Refurbisher
  • Dismantler
  • Recycler
  • Schedule I
  • Schedule II
  • Schedule II A
  • Schedule II B
  • Schedule II C
  • Schedule III
  • Schedule IV
  • Schedule V
  • Bulk consumer
  • End-of-life
  • E-retailer
  • Extended producer responsibility
  • Orphaned products
  • Historical e-waste
  • SPCB
  • CPCB
  • E-Waste Management
  • E-waste management Rules
  • ROHS
  • Reduction in the use of hazardous substances
  • Information technology and telecommunication equipment
  • Consumer Electrical and Electronics and Photovoltaic Panels
  • Large and Small Electrical and Electronic Equipment
  • Electrical and Electronic Tools (With the exception of large- Scale Stationary Industrial tools)
  • Toys
  • Leisure and Sports Equipment
  • Medical Devices (With the Exception of All Implanted and Infected Products)
  • Radiotherapy equipment and accessories
  • MDW1
  • Cardiology equipment and accessories
  • MDW2
  • Dialysis equipment and accessories
  • MDW3
  • Pulmonary ventilators and accessories
  • MDW4
  • Nuclear Medicine Equipment and accessories
  • MDW5
  • Laboratory equipment for in vitro diagnosis and accessories
  • MDW6
  • Analysers and accessories
  • MDW7
  • Magnetic Resonance Imaging (MRI)
  • Positron Emission Tomography (PET) Scanner
  • Computed Tomography (CT) Scanner
  • & Ultrasound Equipment along with accessories
  • MDW8
  • Fertilization tests equipment and accessories
  • MDW9
  • Other electric appliances/equipment/kits used for preventing
  • screening
  • detecting
  • monitoring
  • evaluating
  • reviewing
  • examining
  • investigating
  • probing
  • treating illness sickness
  • disease
  • disorder
  • affliction
  • infection
  • injury
  • trauma
  • abuse or disability including the Mobiles
  • Tablets or any other device with the features having the potential of sex selection and their accessories
  • MDW10
  • Laboratory Instruments

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