Pharmaceutical Investigations - What is Expected?

This webinar provides an overview of investigations in pharmaceutical manufacturing organizations, highlighting the importance of understanding lapses to avoid regulatory action and financial risks.
  • Tuesday
  • August
  • 19
  • 2025
08:00 AM PDT | 11:00 AM EDT
Duration: 60 Minutes
IMG Saurabh Joshi
Webinar Id: 61154
Live
Session
$119.00
Single Attendee
$249.00
Group Attendees
Recorded
Session
$159.00
Single Attendee
$359.00
Group Attendees
Combo
Live+Recorded
$249.00
Single Attendee
$549.00
Group Attendees

Overview:

Investigations are generally triggered when a pharmaceutical manufacturing organization observes a nonconformance and by regulation they need to find out the source, reason, cause of the nonconformance.

Why you should Attend:

Inadequate investigations usually lead to regulatory action, Spoiling of company’s reputation and financial risks. Attending this webinar will help you to understand the usual lapses.

Areas Covered in the Session:

  • Investigation triggers
  • Stages of investigation
  • General misses/lapses
  • How to investigate
  • Root cause identification
  • Real-time example

Who Will Benefit:

  • Managers
  • Sr. Managers
  • Directors

Speaker Profile

Saurabh Joshi has over two decades of industry experience, he led quality in operations, qualifications-validations, QMS, centres of excellence, and consulting. He has studied pharmaceutical sciences and has worked with many reputed pharmaceutical companies in India and an EU based company. He has interacted with regulatory agencies from across the globe including FDA, MHRA, HPRA, WHO (Geneva) and ANVISA. At ValGenesis, Saurabh uses his domain expertise to help customer and clients unleash their true potential by going paperless and transition to Pharma 4.0 journey.