Home  |  About us  |  Editorial board  |  Ahead of print  | Current issue  |  Archives  |  Submit article  |  Instructions |  Search  |   Subscribe  |  Advertise  |  Contacts  |  Login 
  Users Online: 676Home Print this page Email this page Small font sizeDefault font sizeIncrease font size  

 Table of Contents      
Year : 2015  |  Volume : 6  |  Issue : 2  |  Page : 118-119

Indian Regulatory Update: January-March 2015

Head Regulatory Affairs, Boehringer Ingelheim India Pvt. Ltd., Mumbai, Maharashtra, India

Date of Web Publication26-Mar-2015

Correspondence Address:
Kedar Suvarnapathaki
Boehringer Ingelheim India Pvt. Ltd., 1102, 11th Floor, Hallmark Business Plaza, Bandra (E), Mumbai - 400 051, Maharashtra
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2229-3485.154018

Rights and Permissions

How to cite this article:
Suvarnapathaki K. Indian Regulatory Update: January-March 2015. Perspect Clin Res 2015;6:118-9

How to cite this URL:
Suvarnapathaki K. Indian Regulatory Update: January-March 2015. Perspect Clin Res [serial online] 2015 [cited 2022 Jan 17];6:118-9. Available from: https://www.picronline.org/text.asp?2015/6/2/118/154018

This document provides updates in regulatory requirements regarding conduct of clinical trials in India.

   Amended Compensation Rules - GSR 889 (E) Released Top

  • Central Drugs Standard Control Organisation (CDSCO) has issued amended compensation rules providing more clarity on the definition of the term "related to clinical trials (CT)"
  • Clarifications provided for serious adverse event (SAE) reporting timelines to specify that in case of SAE not reported within 24 h of occurrence, the investigator needs to provide reasons for the same
  • Notification also provides better clarity on various other aspects of the compensation rules, the gazette notification can be accessed at following URL: http://www.cdsco.nic.in/writereaddata/Notificatiohn%20on%20Compensation%20on%20clincial%20trial%20 (1).pdf.

   Draft Drugs and Cosmetics (Amendment) Bill, 2015 Top

  • Draft Drugs and Cosmetics (Amendment) bill 2015 has been released for public comments
  • The bill makes the provision for CT under Drugs and Cosmetics Act
  • Provisions also made for import, manufacture, and CT with devices
  • The bill also makes the provisions for CT with cosmetics
  • Penalties have been proposed for various offences like conduct of CT without permission from licensing authority and Expert Committee (EC), violation of conditions of clinical trial permission, not providing compensation, etc
  • Bill makes the provisions for appeal mechanisms for parties aggrieved by the orders under the amended act as well
  • Complete draft of the bill can be accessed at following URL: http://www.cdsco.nic.in/writereaddata/D and %20C%20AMMENDMENT%20BILL%281%29.pdf.

   Drugs and Cosmetics (Third Amendment) Rules 2015 Top

  • Draft amendment of D and C rules as per GSR 69(E) has been released by CDSCO
  • The amendment omits Rule 122DAA which defines a clinical trial, and the definition of clinical trial has been provided as part of the explanation to Rule 122DA
  • The amendment also defines certain terms such as global clinical trial (GCT), IND, and new chemical entity (NCE) as part of the explanation to Rule 122DA along with definition of CT
  • Amendment makes the provision for providing information regarding "assessment of risk versus benefit to patients," "innovation vis-à-vis existing therapeutic option," and "unmet medical need in the country" mandatory as part of form 44 and Appendix I of Schedule Y
  • Draft notification can be accessed at following URL: http://www.cdsco.nic.in/writereaddata/G_S_R_%2069(E).pdf.

   Draft Standards and Application Format for Accreditation of Ethics Committee, Investigator and Clinical Trial Site Top

  • CDSCO has issued draft standards for accreditation of EC and sites as per recommendations of an EC under the Chairmanship of Prof. Ranjit Roy Chaudhury
  • The Ministry of Health and Family Welfare decided to assign the job of accreditation to Quality Council of India
  • The Accreditation Standards and format for application for Accreditation prepared by Quality Council of India are uploaded on CDSCO website for comments/suggestions of stakeholders
  • Accreditation standards and formats can be accessed at following URL: http://cdsco.nic.in/forms/list.aspx?lid=2074 and Id=23.

   Presubmission Meetings Proposed to be Initiated by Central Drugs Standard Control Organisation Top

  • CDSCO has decided to introduce a system of formal Presubmission Meetings of applicants with CDSCO officers and subject experts to discuss regulatory pathway in respect of specific application for approval of clinical trial, new drug, medical device etc
  • The system will facilitate to understand the regulatory pathways required to be followed by the applicants for approvals resulting in bringing transparency, accountability, predictability, and speedy disposal of cases
  • Notice inviting comments for the proposal was issued by CDSCO, the same can be accessed at following URL: http://www.cdsco.nic.in/writereaddata/NOTICE15.pdf.


    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

  In this article
    Amended Compensa...
    Draft Drugs and ...
    Drugs and Cosmet...
    Draft Standards ...
    Presubmission Me...

 Article Access Statistics
    PDF Downloaded536    
    Comments [Add]    

Recommend this journal