Process Risk Management Strategies Reduce Risk and COGS While Improving Yield and Compliance

Jun 21, 2021 - 01:00 PM EST
Starting at

$199


Buy Now

A critical source of risk to patients using pharmaceuticals to improve their health is inadequate design and control of the processes that manufactured the drugs. R&D, Manufacturing, Quality Assurance, Quality Control and Regulatory Affairs play a critical role in reducing risk associated with poorly operating processes. The ICH guidance documents Q8, Q9 and Q10 has heightened awareness in the pharmaceutical and biotech industries of the need to reduce process risk. This trend is also being promoted by the FDA as an approach to process improvement with the benefit of enhanced regulatory flexibility. But the questions remain: What does it mean to reduce risk, to manage risk, and how do you do it? Fortunately we have a lot of experience on which to draw.

Below strategies and the associated guiding principles will be discussed and illustrated with examples and case studies from the pharma and biotech industries. The focus is on reducing risk to reducing cost of goods sold (COGS) while improving process yield and compliance. The discussion also addresses how to make the use of process risk analysis and risk management an integral part of your process management systems, methods and tools.

Areas Covered in the Session :

  • Utilizing the relationship between process variation, process understanding, process risk and compliance
  • Using a systematic approach to identify the critical few variables that have a major impact on the process: Raw materials, process steps, and process variables and uncontrollable (environmental) variables
  • Increasing process stability and capability
  • Creating a process control strategy
  • Robustness studies of the product and process
  • Improvement of measurement performance including improved control and robustness of analytical methods

Who Should Attend:

  • Product Development Scientists
  • Process Development Scientists and Managers
  • Manufacturing Leaders, Staff and Stakeholders
  • Regulatory Affairs Leaders
  • Manufacturing Engineers
  • Quality Assurance Personnel
  • Quality Improvement Engineers
  • Quality Control Personnel
  • Test Method Developers
Webinar Events
Attend Live Webinar
Jun 21, 2021 - 01:00 PM EST

Duration: 90 Minutes

Single Attendee


Group-Max. 10 Attendees/Location (For Multiple Locations Contact Customer Care) Super Deal - Get CD/USB Drive Free!


LIVE + RECORDED VERSION


Training CD-DVD

Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment


Recorded video

Recorded video session




Follow us

24x7 Direct Number
(315) 632-0735,
(315) 750-4379
Toll Free
1-866-978-0800

Fax

1-888-883-7697