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• Formula to Determine the quantum of compensation in the cases of Clinical Trial related serious Adverse Events(SAEs) of Deaths Occuring During Clinical Trials
• Draft Guidelines on Formula to determine the quantum of compensation in case of Clinical Trial related Injury 
• Draft Guidelines on Audio-Visual Recording of Informed Consent Process In Clinical Trial
• Audio -Video Recording of Informed Consent Process of All New Subjects in Clinical Trials- Administrative Orders
• Monitoring of Clinical Trials - regarding
• Details of Global Clinical trial approved in 2012
• Advisory notice on clinical trial  
• Notice: Expansion of panel of experts for evaluation of applications of New Drugs, Clinical Trials and Medical Devices 
• Office Order: Submission of Periodic Safety Update Reports (PSURs)
• New Drugs Recommended by NDAC for marketing authorization in India without Local Clinical Trial (Till August 2012)
• Good Clinical Practice
  
• Draft Guidance For Industry On Requirement Of Chemical & Pharmaceutical Information Including Stability Study Data Before Approval Of Clinical Trials / BE  Studies
  
• DCG(I) approved Clinical Trial registered in Clinical Trial Jan 2013
  
• System of Pre-screening for submission of reports of SAEs to CDSCO
  
• System for the Pre - Screening of the applications for registration of Ethics Committee
  
• Panel of Experts for examination of reports of Serious Adverse Events (SAEs) of Deaths