Watch Now

In the highly regulated Life Sciences Industry, complying with regulations is not an option, it's a necessity. When done correctly compliance programs can add value by improving system performance, increasing user productivity and ensuring data quality. Learn how to apply the right level of control in your regulated laboratory by using an effective risk based approach.

The Best Practices for Laboratory Compliance discussion will include:

  • Ways to streamline effort associated with laboratory compliance
  • How to ensure compliance with regulatory requirements while reducing costs
  • How to stop considering compliance as overhead and instead increase business value through effective compliance programs
  • Live Q & A Session

About the Presenters:

Jim Corwonski
Jim Corwonski

Product Manager Jim got his start as a laboratory chemist before transitioning to lab systems implementation and validation. Jim’s 20 years  of  experience  spans  CSV,  21  CFR  Part 11 compliance, and data integrity, supporting drug and equipment manufacturers, contract labs, and consulting firms in life sciences.

Michael Ambrose
Michael Ambrose

Vice President of Lab and Manufacturing Michael brings over 33 years of life sciences industry experience, specializing in IT and GxP compliance consulting (13 years industry, 20 years as a consultant), focused on delivery of practical and efficient IT solutions and compliance initiatives at the department, site and global level.

Want our experts to work on your project?

Take the first step towards creating more value with USDM today.

Connect Now

We use cookies to understand how you use our site and improve your experience. This includes personalizing content and advertising. Learn more.