Hospital – RMI

Last Updated on August 29, 2021 by The Health Master

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RMI – Recognised Medical Institute – How to get registered

Also read the article: How to get Hospital registered as RMI

If a Hospital uses the following Essential Narcotics Drugs, the registration is required under Narcotic Drugs & Psychotropic Substance (Third Amendment) Rules, 2015 which has come into force vide Gazette notification GSR 359(E) dated 5th May 2015.

Notified Essential Narcotic Drugs (END)
● Morphine
● Codeine
● Methadone
● Hydrocodone
● Oxycodone
● Fentanyl


The Hospital is required to get itself registered as Recognized Medical Institute from the State Drugs Controller of the state.

How to obtain registration of Recognized Medical Institute

For obtaining registration of Recognized Medical Institute, the list of documents required is provided below.

Abbreviations:
NDPS: Narcotic Drugs and Psychotropic Substances
RMI: Recognized Medical Institute
DMP: Designated Medical Practitioner
RMP: Regd. Medical Practitioner
END: Essential Narcotics Drugs
SDC: State Drugs Controller
ASDC: Asstt. State Drugs Controller
SDCO: Senior Drugs Control Officer
DCO: Drugs Control Officer


Instructions to be followed by the Recognised Medical Institutions (RMIs)

  • RMIs shall submit the original application for grant / renewal of Certificate of Recognition as RMI in Form 3F dully filled along with requisite documents to the State Drugs Controller of the state. Copy of the same shall be forwarded to the concerned Asstt. State Drugs Controller / Senior Drugs Control Officer / Drugs Control Officer (as the case may be) of the area.
  • The application shall be accompanied by:
  • Covering letter addressed to the SDC signed by the Medical Officer in charge of the RMI.
  • Application for issue / renewal of Certificate of Recognition as RMI in Form 3F.
  • Estimate of annual requirement of Essential Narcotic Drugs (END) in Form 3J.
  • Constitution of RMI
  • ROC certificate of RMI
  • List of Directors / Partners with address
  • Affidavits of Directors / Partners / Proprietor
  • MoA of RMI

  • Form-32 of all directors
  • Partnership deed
  • BOD Resolution
  • Authorization letter for In-Charge
  • Affidavit of In-Charge
  • Authorization letter for Designated Medical Practitioner (DMP)
  • Affidavit of DMP
  • List of Regd. Medical Practitioners (RMP) with Qlf., Regn. No. Mobile No etc.
  • Self attested copies of Registration and Qualification Certificates of the in-charge / DMP / RMPs of RMI (in case of Fresh RMI application / change in Medical Officer).
  • Copy of the certificate in proof of pain management training as notified in NDPS Rules (in case of Fresh RMI application / change in Medical Officer).

  • Storage of END ( Cupboard with double lock system)
  • Blue print map of the premises.
  • Ownership / rent / lease deed
  • Electricity bill of RMI
  • Pan card of the RMI
  • Fire safety certificate
  • Genset
  • Other medical certificate ( PNDT, MTP etc)
  • Annual return of procurement / disbursement of END in Form 3-I (in case of Renewal of RMI).
  • Original of RMI certificate in Form 3G (in case of renewal of RMI).
  • Details of suppliers from whom the END are procured.

Checklist for RMI

To download the checklist in pdf file for obtaining registration as Recognized Medical Institute. Click below link

Forms

Download the below pdf files for various Forms which are required after obtaining registration as Recognized Medical Institute.

Submit your application to State Drugs Controller / Licensing Authority of your area after completing all the required documents.

Specimen Affidavits for RMI

Download the below pdf files for specimen affidavits which are required after obtaining registration as Recognized Medical Institute.

Note: Requirements of some of documents and procedure for submission of application may vary from State to State


Conditions of RMI

  1. Certificate of Recognition (RMI) shall be valid for 3 years.
  2. Application for the renewal of RMI shall be made to the SDC at least 60 days before the expiry.
  3. Every RMI shall be liable to periodic inspections by the ASDC / SDCO / DCO authorized by the SDC.
  4. In the event of change in constitution of RMI, the current Recognition shall be deemed to be cancelled if the same is not intimated to the SDC within 90 days of such change.
  5. Change in Medical Officer / change in name of the RMI shall be intimated to the SDC immediately.
  6. Copy of every consignment note of END in Form 3C dully filled and signed by both the consigner and consignee, shall be forwarded to the SDC. Original of the same shall be retained by the RMIs for a period of 2 years from the date of transaction and such records shall be produced before the officer on demand during inspection.
  7. Every RMI shall also maintain a separate record as per Form 3E for each patient and such records shall be retained for period of 2years from the date of last entry. This record shall be produced before the officer on demand during inspection.
  8. Every RMI shall maintain daily accounts of all receipts and dispensed quantities for each END as per Form 3H, which shall be retained for a period of 2 years from the date of last entry. This record shall be produced before the officer on demand during inspection.
  9. Every RMI shall submit an estimate of its annual requirement of END in Form 3-J by 30th November of the proceeding calendar year to the SDC.
  10. If the disbursement of the END exceeds the estimate of annual requirement in Form 3J, a revised estimate shall be submitted in Form 3J in due course.
  11. Details of suppliers of END other than regular suppliers shall be intimated in due course.
  12. RMIs shall file annual return of procurement / disbursement of essential narcotic drugs for a calendar year on or before 31st of March of the subsequent year in Form 3 I to the SDC.
  13. The Medical Officer in charge of the RMI shall record a brief justification were the annual disbursement is more than 10% of the estimate or revised estimate along with Form 3 I.

Forms for regular reporting

List of Forms for for regular reporting to the authorities are provided below. Download the pdf file and prepare the reports accordingly.


For notifications of RMI, click below link:

Notifications – RMI


Disposal of Essential Narcotic drugs

By a registered RMI (Hospital)

Rule 52S: Disposal of drugs on surrender of recognition:

On surrender of the recognition, the essential narcotic drugs as may be in the possession of the RMI shall be disposed of in su h manner, including transfer to another RMI, as may be specified by the Controller of Drugs

By a manufacturer

Rule 45A: Destruction of drugs:

(1) A licensee seeking to destroy the drug shall apply to the Narcotic Commissioner in such form and manner as may be specified by the Narcotic Commissioner

(2) The Narcotic Commissioner shall, within a period of thirty days from the date of receipt of an application under sub-rule (1), appoint a committee comprising of a Gazetted Officer in the office of the Narcotic Commissioner, or Narcotic Control Bureau constituted vide notification number S.O. 96(E) dated 17-03-1986, Superintendent of Central Excise of the concerned range and an authorized representative of the applicant for supervising the destruction of the drug and such such destruction shall be carried out within a period of thirty days from the appointment of the committee.

(3) The destruction of the drug shall be carried out in accordance with the provision of the relevant laws for the time being in force.

By a Authorized person or registered medical practitioner

Rule 52M: Disposal of stocks of essential narcotic drugs on expiry, surrender, cancellation of authorization:

(1) Such stock of essential narcotic drugs as may be in the possession of an authorized person, on the expiry or cancellation or surrender of his authorization, shall be disposed of in such manner as may be specified by the Controller of Drugs in this behalf.

(2) The expired stock of essential narcotic drugs as may be in the possession of an authorized person or a registered practitioner shall be destroyed in such manner as may be specified by the Controller of Drugs.

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