Register for our Live Webinar:
Thursday, December 7, 2023 | 11am EST | 8am PST | 5pm CET

Event Overview

Maintaining compendia compliance in a rapidly changing and unpredictable industry magnifies the complexity of testing raw materials. Adapting to the constant flux of a dynamic and unpredictable industry poses significant complexity to maintain compliance, especially with ever evolving global compendia. Monitoring multiple compendia (USP, EP, BP, JP) for updates, revisions, new text, etc. is a manual and tedious process. Do you have the expertise, staff and time to perform the daily tasks required to remain compliant with compendia updates?

In this webinar, we will explore the complexities of compendia surveillance and Eurofins BioPharma Product Testing’s processes and industry leadership position in maintaining compliance, including:
  • Processes needed to properly monitor global compendia
  • Technology-based solutions for information management
  • Information sharing across the Eurofins global network
  • Relationship with the USP
  • Industry involvement and leadership in updates and new content

Presenters:

Matt Rodak DSC_0068_300px.JPG
 Matt Rodak
Senior Manager
Eurofins BioPharma Product Testing
As a Senior Manager at Eurofins BioPharma Product Testing, Mr. Rodak oversees the Raw Materials QC testing group at the Lancaster, PA facility. He has 18 years of experience in raw materials testing. Mr. Rodak earned a BS in biochemistry from Lipscomb University and an MBA from West Chester University.

Lyndsey Renninger_300px.jpg
 Lyndsey Renninger
Manager
Eurofins BioPharma Product Testing
As a Manager at Eurofins BioPharma Product Testing, Miss Renninger oversees the Raw Materials QC testing group at the Lancaster, PA facility. She has 12 years of experience in raw materials testing services specializing in small molecule chemistry testing following a variety of compendia and other material specific procedures. Miss Renninger earned a BS in biochemistry from Albright College.



Register for our On Demand Webinar

Event Overview

Maintaining compendia compliance in a rapidly changing and unpredictable industry magnifies the complexity of testing raw materials. Adapting to the constant flux of a dynamic and unpredictable industry poses significant complexity to maintain compliance, especially with ever evolving global compendia. Monitoring multiple compendia (USP, EP, BP, JP) for updates, revisions, new text, etc. is a manual and tedious process. Do you have the expertise, staff and time to perform the daily tasks required to remain compliant with compendia updates?

In this webinar, we will explore the complexities of compendia surveillance and Eurofins BioPharma Product Testing’s processes and industry leadership position in maintaining compliance, including:
  • Processes needed to properly monitor global compendia
  • Technology-based solutions for information management
  • Information sharing across the Eurofins global network
  • Relationship with the USP
  • Industry involvement and leadership in updates and new content

Presenters:

Matt Rodak DSC_0068_300px.JPG
 Matt Rodak
Senior Manager
Eurofins BioPharma Product Testing
As a Senior Manager at Eurofins BioPharma Product Testing, Mr. Rodak oversees the Raw Materials QC testing group at the Lancaster, PA facility. He has 18 years of experience in raw materials testing. Mr. Rodak earned a BS in biochemistry from Lipscomb University and an MBA from West Chester University.

Lyndsey Renninger_300px.jpg
 Lyndsey Renninger
Manager
Eurofins BioPharma Product Testing
As a Manager at Eurofins BioPharma Product Testing, Miss Renninger oversees the Raw Materials QC testing group at the Lancaster, PA facility. She has 12 years of experience in raw materials testing services specializing in small molecule chemistry testing following a variety of compendia and other material specific procedures. Miss Renninger earned a BS in biochemistry from Albright College.