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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 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:

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.

James Corwonski

Validation and Compliance Consultant, USDM Life Sciences James has his professional roots in industrial and pharmaceutical chemical labs.  As a computer geek before it was cool, he naturally embraced the automation surge of the late nineties and early two-thousands and evolved into a computer compliance specialist as the industry demanded.

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