Professional Documents
Culture Documents
3
E-Waste (Management) Rules, 2016.
Sweden
I 2005
Japan
USA I 1998
I 2003 Switzerland C 2012
C 2010 I 1998
C 2003
Germany
I 1994
C 2012
Ethiopia
NA China
I 2000
C 2011
India
I 2011
Uganda C 2016
I 2009
C - 2012
Legend Tanzania
I Year of Inception NA
C Current legislation
4
E-Waste (Management) Rules, 2016.
Key Terms
Bulk consumer Turnover of 1 Cr or more Recycler
than 20 employees
Refurbisher
Collection centre
Target
Deposit refund scheme
Dismantler
End-of-life and Disposal
Extended Producer Responsibility (EPR)
Producer Responsibility Organisation (PRO)
5
E-Waste (Management) Rules, 2016.
MANUFACTURER/
PRODUCER
retailer/dealer
CONSUMER/
BULK CONSUMER
END of LIFE collection/transport
equipment e-waste
COLLECTION CENTRES
storage & transport
REFURBISHER/
DISMANTLER / RECYCLER
6
E-Waste (Management) Rules, 2016.
Chapters
Chapter I General includes applicability and definitions of the terminologies used in
these rules.
Chapter II Responsibilities of stakeholders manufacturer, producer, collection centres,
dealers, refurbisher, consumer, dismantler, recycler.
Chapter III Procedures for seeking & grant of Authorization.
Chapter IV Procedure for Storage of e-waste.
Chapter V Reduction in use of Hazardous Substances (RoHS).
Chapter VI Miscellaneous includes Duties of Authorities, Annual Report, Transportation
of e-waste, Accident reporting, liability and appeal.
7
E-Waste (Management) Rules, 2016.
The E-waste (M) Rules, 2016 include 3 Schedules and 10 Forms prescribed for
submission of information:
Schedule I Categories of electrical and electronic equipments
Schedule II RoHS exemptions
Schedule III Targets for EPR Authorization
Schedule IV List of Authorities & their duties.
8
E-Waste (Management) Rules, 2016.
9
E-Waste (Management) Rules, 2016.
Responsibilities of manufacturer
Collect waste during manufacturing and recycle or dispose
Seek authorization
Maintain records; File returns
Responsibilities of Producer
Collection and channelization
EPR - Authorization
Deposit Refund Scheme (DRS)
Individual/Collective Producer Responsibility
Pretreatment
10
E-Waste (Management) Rules, 2016.
Collection of E-Waste
Responsibility of Producer/Dismantler/Recycler/Refurbisher individually or
collectively
Storage of E-Waste
Manufacturer, Producer, bulk consumer, collection centre, dealer,
refurbisher, dismantler or recyclers can store the e-waste for a period of
180 days.
11
E-Waste (Management) Rules, 2016.
MANUFACTURER
AUTHORIZATION PRODUCER
Form 1, 1(a),1(aa)
REFURBISHER
DISMANTLER
RECYLERS
13
E-Waste (Management) Rules, 2016.
MANUFACTURER/PRODUCERS
DEALERS
CONSUMERS
REFURBISHERS
DISMANTLERS/ECYLERS
14
E-Waste (Management) Rules, 2016.
MANUFACTURERS/PRODUCERS
REFURBISHER
FILING OF RETURNS
(Form 3)
DISMANTLERS/RECYLERS
15
E-Waste (Management) Rules, 2016.
16
Bio-Medical Waste Management
Rules, 2016
Let the waste of the sick not contaminate the lives of The Healthy
17
Bio-Medical Waste Management
Rules, 2016
Bio-medical waste: Any waste which is generated during the diagnosis,
treatment, or immunization of human beings or animals or research
activities or in the production or testing of biologicals or in health camps.
Prescribed authority: State Pollution Control Board/Committee
Bio-medical waste treatment and disposal facility (CBMWTF)
Occupier
Operator of a CBMWTF
18
Bio-Medical Waste Management
Rules, 2016
Duties of Occupier
Ensure that bio-medical waste is handled without any adverse effect
to human health and environment
Shall be segregated at the point of generation as per the colour codes
in Schedule I.
Bio-medical waste shall not be mixed with any other waste
Segregation, packaging, transport and storage in accordance with
Schedule I and in compliance with standards in Schedule II
19
Bio-Medical Waste Management
Rules, 2016
Duties of Operator of CBMWTF
Timely collection from occupier, treatment and disposal Schedule I
and in compliance with standards in Schedule II
Establish Bar coding and Global positioning system
Maintain a log book and all records for at least 5 years
Provide training and ensure safety of all workers handling waste
Display details of authorisation, treatment, annual report etc on its
web-site
20
Bio-Medical Waste Management
Rules, 2016
Authorisation
Given by State Pollution Control Board/Committee
Applications for seeking authorisation to be disposed within 90 days
Power to refuse or renew and cancel or suspend
One time for non-bedded and periodic renewal for bedded
establishments
Publish the list of Registered or Authorised (or give consent) Recyclers.
21
Bio-Medical Waste Management
Rules, 2016
Prescribed Authorities
MoEFCC Policies, financial assistance for setting up of CBMWTF,
Research and Manual for training.
Central/State Health Ministry Publish list of registered facilities,
Training programmes
CPCB Prepare guidelines, Technology standards, Inspection and
monitoring.
Municipality/Local bodies Allocate land for setting up of CBMWTF
22
Bio-Medical Waste Management
Rules, 2016
23
Bio-Medical Waste Management
Rules, 2016
Records
Accident Reporting Form I
Authorisation Form II and III
Annual reports (Returns) Form-IV, on or before the 30th June of
every year.
Maintenance of records related to generation, collection, reception,
storage, transportation, treatment, disposal or any other from of
handling of bio-medical waste Log books and records
24
Bio-Medical Waste Management
Rules, 2016
Waste category Colour code Treatment
Human anatomical waste, Animal Yellow Inc./ Plasma Pyrolysis/ burial
waste, Soiled Waste
Discarded Medicines, Cytotoxic drugs Yellow Inc./Send back to manufacturer
Microbiology & biotechnology waste Yellow Inc. (after lab pre treatment)
25
Bio-Medical Waste Management
Rules, 2016
Waste category Colour code Treatment
Contaminated/Recyclable Waste Red Autoclave/ hydroclaving/
microwaving; shredding;
recycling
Waste Sharps White/ translucent Autoclave/Shredding; landfill
(puncture proof)
Glassware (expect Cytotoxic Blue Cardboard boxes Disinfection/autoclave/
contaminated), Metallic Body hydroclaving/ microwaving;
Implants recycling
26
Bio-Medical Waste Management
Rules, 2016
27
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
First rules published in 1989. Revisions in 2008 and 2016
Applies to all generators, occupiers, actual users, operators who carry
out the activities of generation, handling, collection, reception,
treatment, transport, storage, reuse, recycling, recovery, pre-
processing, utilisation, including co-processing and disposal of
hazardous wastes
Hazardous waste means any waste which by reason of characteristics
such as physical, chemical, biological, reactive, toxic, flammable,
explosive or corrosive, causes danger or is likely to cause danger to
health or environment, whether alone or in contact with other wastes
or substances
28
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Key terms
Occupier and Actual user
Basel Convention
Captive and Common treatment, storage and disposal facility
Operator of disposal facility
Disposal
Pre-processing and Co-processing
29
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Manifest
Other wastes
Recycling, Reuse, Recovery
Transboundary movement
Environmentally sound technologies
30
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Chapters
1 PRELIMINARY
2 - PROCEDURE FOR MANAGEMENT OF HAZARDOUS AND OTHER WASTES
3 - IMPORT AND EXPORT OF HAZARDOUS AND OTHER WASTES
4 - TREATMENT, STORAGE AND DISPOSAL FACILITY FOR HAZARDOUS AND
OTHER WASTES
5 - PACKAGING, LABELLING, AND TRANSPORT OF HAZARDOUS AND OTHER
WASTES.
6 MISCELLANIOUS
31
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Schedules
1 List of processes generating hazardous wastes
2 - List of waste constituents with concentration limits
3 - List of hazardous wastes applicable for import and export with and without Prior Informed
Consent (PIC) and based on hazardous characteristics
4 - List of commonly recyclable hazardous wastes
5 - Specifications of Used Oil Suitable for recycling and specifications of fuel from oil
6 Hazardous and Other waste prohibited for Import
7 - List of authorities and corresponding duties
8 - List of documents for verification by Customs for import of other wastes 32
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Forms
1 Application required for grant/renewal of authorisation
2 Grant or Renewal of Authorisation
3 Maintaining records of Hazardous and Other waste
4 Filing of Annual returns
5 Application for Import and Export of Hazardous and Other waste
6 Transboundary movement movement document
8 Labeling of containers of Hazardous and other waste
9 Transport Emergency Card (TREM)
10 Manifest for Hazardous and other waste
11 Format for reporting accident 33
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Responsibilities of Occupier prevention; minimization; reuse, recycling; recovery, utilisation including
co-processing; safe disposal.
Waste to be sold/sent to authorised actual user or shall be disposed of in an authorised disposal facility.
Maintain records
Storage not more 90 days;
Actual users and disposal facility operators up to 180 days
36
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Manifest system
37
Hazardous and Other Wastes
(Management and Transboundary Movement) Rules, 2016
Responsibilities of Authorities
MoEFCC Identification of hazardous and other wastes, Permission export, import
and transit waste.
CPCB Training of authorities, Co-ordination with SPCB, Recommend standards,
Review annual report of Hazardous and other waste, Prepare guidelines, SOPs and
Manual.
SPCB Grant and Renewal of authorization, Monitoring of compliance, Examining
applications for import and forwarding to MoEFCC
Directorate general of Foreign Trade and Ports authority
38
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Dr.Prasad Modak, Ekonnect Knowledge Foundation
Address:
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Bandra (East) Mumbai 400 051
Tel : 91 022 6221 5944/5946
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Ekonnect Knowledge Foundation is a not for profit company offering education and awareness on Environment, CSR & Sustainability.
CDEM is a program conceived and organized by K.J.Somaiya in partnership with and support of MMR-EIS.
This module 1 is part of the 5 module diploma certificate offered under this program.