Learn about the evolution of
quality culture in the
Indian pharmaceutical industry
 
24th March, 2015
9.00 a.m. to 5.00 p.m.
ITC Maratha, Mumbai, India
 
To spearhead the changing paradigms of the pharmaceutical regulatory compliance and training,
UL, in association with IDMA organizes a one-day summit on
 
“Taking Pharma Quality Culture to the Next Level: Roadmap for Handling FDA Audits,
Inspections, and CAPA”
 
The sessions would focus on management of FDA audits, inspections and CAPA with training. From some of the
global experts on compliance and regulatory of pharmaceutical industry, you will have insight into:
 
  • The role of leadership in building a compliance culture in their organization
  • Understand how proper learning tools can help build compliance and improve performance
  • Identify key areas of improvement to build compliance across quality & operation functions.
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    For more information contact:
    Anand Iyer / E: Anand.iyer@ul.com / M: +91 9619667138
    UL EduNeering, India
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