Ministry of Environment & Forests
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S.O. 630 (E).-Whereas a notification in exercise of the powers conferred by Sections 6, 8 and 25 of the Environment (Protection) Act, 1986 (29 of
1986) was published in the Gazette vide S.O. 746 (E) dated 16 October, 1997 inviting objections from the public within 60 days from the date of the
publication of the said notification on the Bio-Medical Waste (Management and Handling) Rules, 1998 and whereas all objections received were
duly considered..
Now, therefore, in exercise of the powers conferred by section 6, 8 and 25 of the Environment (Protection) Act, 1986 the Central Government hereby
notifies the rules for the management and handling of bio-medical waste.
(1) These rules may be called the Bio-Medical Waste (Management and Handling) Rules, 1998.
(2) They shall come into force on the date of their publication in the official Gazette.
APPLICATION:
These rules apply to all persons who generate, collect, receive, store, transport, treat, dispose, or handle bio medical waste in any form.
(1) "Act" means the Environment (Protection) Act, 1986 (29 of 1986);
(2) "Animal House" means a place where animals are reared/kept for experiments or testing purposes;
(3) "Authorisation" means permission granted by the prescribed authority for the generation, collection, reception, storage, transportation,
treatment, disposal and/or any other form of handling of bio-medical waste in accordance with these rules and any guidelines issued by the
Central Government.
(4) "Authorised person" means an occupier or operator authorised by the prescribed authority to generate, collect, receive, store, transport,
treat, dispose and/or handle bio-medical waste in accordance with these rules and any guidelines issued by the Central Government;
(5) "Bio-medical waste" means any waste, which is generated during the diagnosis, treatment or immunisation of human beings or animals or
in research activities pertaining thereto or in the production or testing of biologicals, and including categories mentioned in Schedule I;
(6) "Biologicals" means any preparation made from organisms or micro-organisms or product of metabolism and biochemical reactions
intended for use in the diagnosis, immunisation or the treatment of human beings or animals or in research activities pertaining thereto;
(7) "Bio-medical waste treatment facility" means any facility wherein treatment. disposal of bio-medical waste or processes incidental to
such treatment or disposal is carried out;
(8) "Occupier" in relation to any institution generating bio-medical waste, which includes a hospital, nursing home, clinic dispensary,
veterinary institution, animal house, pathological laboratory, blood bank by whatever name called, means a person who has control over that
institution and/or its premises;
(9) "Operator of a bio-medical waste facility" means a person who owns or controls or operates a facility for the collection, reception,
storage, transport, treatment, disposal or any other form of handling of bio-medical waste;
4. DUTY OF OCCUPIER:
It shall be the duty of every occupier of an institution generating bio-medical waste which includes a hospital, nursing home, clinic, dispensary,
veterinary institution, animal house, pathological laboratory, blood bank by whatever name called to take all steps to ensure that such waste is
handled without any adverse effect to human health and the environment.
(1) Bio-medical waste shall be treated and disposed of in accordance with Schedule I, and in compliance with the standards prescribed in
Schedule V.
(2) Every occupier, where required, shall set up in accordance with the time-schedule in Schedule VI, requisite bio-medical waste treatment
facilities like incinerator, autoclave, microwave system for the treatment of waste, or, ensure requisite treatment of waste at a common waste
treatment facility or any other waste treatment facility.
(2) Bio-medical waste shall be segregated into containers/bags at the point of generation in accordance with Schedule II prior to its storage,
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transportation, treatment and disposal. The containers shall be labeled according to Schedule III.
(3) If a container is transported from the premises where bio-medical waste is generated to any waste treatment facility outside the premises,
the container shall, apart from the label prescribed in Schedule III, also carry information prescribed in Schedule IV.
(4) Notwithstanding anything contained in the Motor Vehicles Act, 1988, or rules thereunder, untreated biomedical waste shall be transported
only in such vehicle as may be authorised for the purpose by the competent authority as specified by the government.
(5) No untreated bio-medical waste shall be kept stored beyond a period of 48 hours
Provided that if for any reason it becomes necessary to store the waste beyond such period, the authorised person must take permission of the
prescribed authority and take measures to ensure that the waste does not adversely affect human health and the environment.
7. PRESCRIBED AUTHORITY
(1) The Government of every State and Union Territory shall establish a prescribed authority with such members as may be specified for
granting authorisation and implementing these rules. If the prescribed authority comprises of more than one member, a chairperson for the
authority shall be designated.
(2) The prescribed authority for the State or Union Territory shall be appointed within one month of the coming into force of these rules.
(3) The prescribed authority shall function under the supervision and control of the respective Government of the State or Union Territory.
(4) The prescribed authority shall on receipt of Form 1 make such enquiry as it deems fit and if it is satisfied that the applicant possesses the
necessary capacity to handle bio-medical waste in accordance with these rules, grant or renew an authorisation as the case may be.
(5) An authorisation shall be granted for a period of three years, including an initial trial period of one year from the date of issue. Thereafter,
an application shall be made by the occupier/operator for renewal. All such subsequent authorisation shall be for a period of three years. A
provisional authorisation will be granted for the trial period, to enable the occupier/operator to demonstrate the capacity of the facility.
(6) The prescribed authority may after giving reasonable opportunity of being heard to the applicant and for reasons thereof to be recorded in
writing, refuse to grant or renew authorisation.
(7) Every application for authorisation shall be disposed of by the prescribed authority within ninety days from the date of receipt of the
application.
(8) The prescribed authority may cancel or suspend an authorisation, if for reasons, to be recorded in writing, the occupier/operator has failed
to comply with any provision of the Act or these rules :
Provided that no authorisation shall be cancelled or suspended without giving a reasonable opportunity to the occupier/operator of being heard.
8. AUTHORISATION
(1) Every occupier of an institution generating, collecting, receiving, storing, transporting, treating, disposing and/or handling bio-medical
waste in any other manner, except such occupier of clinics, dispensaries, pathological laboratories, blood banks providing treatment/service to
less than 1000 (one thousand) patients per month, shall make an application in Form 1 to the prescribed authority for grant of authorisation.
(2) Every operator of a bio-medical waste facility shall make an application in Form 1 to the prescribed authority for grant of authorisation.
(3) Every application in Form 1 for grant of authorisation shall be accompanied by a fee as may be prescribed by the Government of the State
or Union Territory.
9. ADVISORY COMMITTEE
The Government of every State/Union Territory shall constitute an advisory committee. The committee will include experts in the field of
medical and health, animal husbandry and veterinary sciences, environmental management, municipal administration, and any other related
department or organisation including non-governmental organisations. The State Pollution Control Board/Pollution Control Committee shall
be represented. As and when required, the committee shall advise the Government of the State/Union Territory and the prescribed authority
about matters related to the implementation of these rules.
Every occupier/operator shall submit an annual report to the prescribed authority in Form 11 by 31 January every year, to include information
about the categories and quantities of bio-medical wastes handled during the preceding year. The prescribed authority shall send this
information in a compiled form to the Central Pollution Control Board by 31 March every year.
(1) Every authorised person shall maintain records related to the generation, collect ' ion, reception, storage, transporation, treatment, disposal
and/or any form of handling of bio-medical waste in accordance with these rules and any guidelines issued.
(2) All records shall be subject to inspection and verification by the prescribed authority at any time.
When any accident occurs at any institution or facility or any other site where bio-medical waste is handled or during transportation of such
waste, the authorised person shall report the accident in Form Ill to the prescribed authority forthwith.
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13. APPEAL
Any person aggrieved by an order made by the prescribed authority under these rules may, within thirty days from the date on which the order
is communicated to him, prefer an appeal to such authority as the Government of State/Union Territory may think fit to constitute :
Provided that the authority may entertain the appeal after the expiry of the said period of thirty days if it is satisfied that the appellant was
prevented by sufficient cause from filing the appeal in time.
SCHEDULE I
(See Rule 5)
@@ Chemicals treatment using at least 1% hypochlorite solution or any other equivalent chemical reagent. It must be ensured that chemical
treatment ensures disinfection.
@ There will be no chemical pretreatment before incineration. Chlorinated plastics shall not be incinerated.
* Deep burial shall be an option available only in towns with population less than five lakhs and in rural areas.
SCHEDULE II
(see Rule 6)
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Cat. 6.
destruction/shredding
Notes:
1. Colour coding of waste categories with multiple treatment options as defined in Schedule I, shall be selected depending on treatment option
chosen, which shall be as specified in Schedule I.
2. Waste collection bags for waste types needing incineration shall not be made of chlorinated plastics.
SCHEDULE III
(see Rule 6)
SCHEDULE IV
(see Rule 6)
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Phone No.
Note :
Label shall be non-washable and prominently visible.
SCHEDULE V
All incinerators shall meet the following operating and emission standards
A. Operating Standards
4. The secondary chamber gas residence time shall be at least I (one) second at 1050 � 50 C�, with minimum 3% Oxygen in the stack gas.
B. Emission Standards
Note :
� Suitably designed pollution control devices should be installed/retrofitted with the incinerator to achieve the above emission limits, if
necessary.
� Wastes to be incinerated shall not be chemically treated with any chlorinated disinfectants.
� Toxic metals in incineration ash shall be limited within the regulatory quantities as defined under the Hazardous Waste (Management and
Handling Rules,) 1989.
� Only low sulphur fuel like L.D.0dLS.H.S.1Diesel shall be used as fuel in the incinerator.
The autoclave should be dedicated for the purposes of disinfecting and treating bio-medical waste,
(I) When operating a gravity flow autoclave, medical waste shall be subjected to :
(i) a temperature of not less than 121 C' and pressure of 15 pounds per square inch (psi) for an autoclave residence time of not less than
60 minutes; or
(ii) a temperature of not less than 135 C� and a pressure of 31 psi for an autoclave residence time of not less than 45 minutes; or
(iii) a temperature of not less than 149 C� and a pressure of 52 psi for an autoclave residence time of not less than 30 minutes.
(II) When operating a vacuum autoclave, medical waste shall be subjected to a minimum of one pre-vacuum pulse to purge the autoclave of all
air. The waste shall be subjected to the following:
(i) a temperature of not less than 121 C� and pressure of 15 psi per an autoclave residence time of not less than 45 minutes; or
(ii) a temperature of not less than 135 C� and a pressure of 31 psi for an autoclave residence time of not less than 30 minutes;
(III) Medical waste shall not be considered properly treated unless the time, temperature and pressure indicators indicate that the required time,
temperature and pressure were reached during the autoclave process. If for any reasons, time temperature or pressure indicator indicates that
the required temperature, pressure or residence time was not reached, the entire load of medical waste must be autoclaved again until the
proper temperature, pressure and residence time were achieved.
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Each autoclave shall have graphic or computer recording devices which will automatically and continuously monitor and record dates, time of
day, load identification number and operating parameters throughout the entire length of the autoclave cycle.
Spore testing :
The autoclave should completely and consistently kill the approved biological indicator at the maximum design capacity of each autoclave
unit. Biological indicator for autoclave shall be Bacillus stearothermophilus spores using vials or spore Strips; with at least 1X104 spores per
millilitre. Under no circumstances will an autoclave have minimum operating parameters less than a residence time of 30 minutes, regardless
of temperature and pressure, a temperature less than 121 C� or a pressure less than 15 psi.
A chemical indicator strip/tape the changes colour when a certain temperature is reached can be used to verify that a specific temperature has
been achieved. It may be necessary to use more than one strip over the waste package at different location to ensure that the inner content of
the package has been adequately autoclaved
The effluent generated from the hospital should conform to the following limits
PARAMETERS PERMISSIBLE LIMITS
PH 63-9.0
Susponded solids 100 mg/l
Oil and grease 10 mg/l
BOD 30 mg/l
COD 250 mg/l
Bio-assay test 90% survival of fish after 96 hours in 100% effluent.
these limits are applicable to those, hospitals which are either connected with sewers without terminal sewage treatment plant or not connected
to public sewers. For discharge into public sewers with terminal facilities, the general standards as notified under the Environment (Protection)
Act, 1986 shall be applicable.
STANDARDS OF MICROWAVING
1 Microwave treatment shall not be used for cytotoxic, hazardous or radioactive wastes, contaminated animal car casses, body parts and large
metal items.
2. The microwave system shall comply with the efficacy test/routine tests and a performance guarantee may be provided by the supplier before
operation of the limit.
3. The microwave should completely and consistently kill the bacteria and other pathogenic organisms that is ensured by approved biological
indicator at the maximum design capacity of each microwave unit. Biological indicators for microwave shall be Bacillus Subtilis spores using
vials or spore strips with at least 1 x 101 spores per milliliter.
1. A pit or trench should he dug about 2 meters deep. It should be half filled with waste, then covered with lime within 50 cm of the surface,
before filling the rest of the pit with soil.
2. It must be ensured that animals do not have any access to burial sites. Covers of galvanised iron/wire meshes may be used.
3. On each occasion, when wastes are added to the pit, a layer of 10 em of soil shall be added to cover the wastes.
5. The deep burial site should be relatively impermeable and no shallow well should be close to the site.
6. The pits should be distant from habitation, and sited so as to ensure that no contamination occurs of any surface water or ground water. The
area should not be prone to flooding or erosion.
7. The location of the deep burial site will be authorised by the prescribed authority.
8. The institution shall maintain a record of all pits for deep burial.
SCHEDULE VI
(see Rule 5)
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and above
B. Hospitals and nursing homes in towns with population of below
30 lakhs,
(a) with 500 beds and above by 31st December, 1999 or earlier
(b) with 200 beds and above but less than 500 beds by 31st December, 2000 or earlier
(c) with 50 beds and above but less than 200 beds by 31st December, 2001 or earlier
(d) with less than 50 beds by 31st December, 2002 or earlier
C. All other institutions generating bio-medical waste not included by 31st December, 2002 or earlier
in A and B above
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FORM I
(see rule 8)
To
1. Particulars of Applicant
(i) Generation
(ii) Collection
(iii) Reception
(iv) Storage
(v) Transportation
(vi) Treatment
(vii) Disposal
(viii) Any other form of handling
5.
7.
8. Declaration
I do hereby declare that the statements made and information given above are true to the best of my knowledge and belief and that I have
not concealed any information.
I do also hereby undertake to provide any further information sought by the prescribed authority in relation to these rules and to fulfill
any conditions stipulated by the prescribed authority.
Date : Signature of the Applicant
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FORM II
ANNUALREPORT
Address
Tel. No
Telex No.
Fax No.
Place.............................. Designation..........................................
FORM III
ACCIDENT REPORTING
4. Assessment of the effects of the accidents on human health and the environment,.
Place.............................. Designation..........................................
[F.No.23-2/96-HSMD]
VIJAY SHARMA, Jt.Secy.
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