Digital Continued Process Verification-The Stage-III of Process Validation using Technology

This webinar focuses on digitization for compliant, agile, sustainable, and quality product delivery. It highlights the importance of continued process verification (CPV) in Pharma 4.0 journey, highlighting the need for digital CPV beyond paper-based or hybrid methods.
  • Tuesday
  • July
  • 22
  • 2025
08:00 AM PDT | 11:00 AM EDT
Duration: 60 Minutes
IMG Saurabh Joshi
Webinar Id: 61152
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:

Continued process verification/validation is that stage of product manufacturing where monitoring, improvement and evidence of control is demonstrated. We will dwell in subject of digitalization and how it will bring more value to current state of CPV.

Why you should Attend:

Digitization is an objective for organizations that want to be compliant, agile, sustainable and improve the efficiency of delivering a quality product to patients. CPV or continued process verification is a tool (Stage-III of process validation) that enables you to ensure that you don’t only make a product that performs as expected but also that you understand variability and possible improvement opportunities in process. This webinar will go beyond paper-based or Hybrid CPV to help you understand that without using digital CPV you’re still far from your Pharma 4.0 journey and a better product realization.

Areas Covered in the Session:

  • Basic understanding of CPV
  • What is digital CPV
  • How it changes monitoring dynamics
  • Benefits of digital CPV

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.