Blogs

Whitehouse Laboratories To Participate On The Medical Device Reprocessing Panel Discussion At MD&M East

2018-05-10T07:13:26+00:00

MD&M East Schedule Whitehouse Laboratories is excited to announce that it has accepted an invitation to participate on the [...]

Whitehouse Laboratories To Participate On The Medical Device Reprocessing Panel Discussion At MD&M East 2018-05-10T07:13:26+00:00

What the Ever-Changing Revisions to USP <661> Really Mean & How the Industry is Responding

2018-05-10T07:13:26+00:00

John Iannone, Director, Extractables & Leachables (John.Iannone@amriglobal.com) Brandon Zurawlow, Associate Director, Container Qualification & CCIT (Brandon.Zurawlow@amriglobal.com) May, 2017 Recently, USP [...]

What the Ever-Changing Revisions to USP <661> Really Mean & How the Industry is Responding 2018-05-10T07:13:26+00:00

Proposed Revisions to ISO 11607 – The Potential Impact on Medical Device Performance Testing

2018-05-10T07:13:26+00:00

Highlights of Proposed Revisions to ISO 11607 Adapted from HealthPack 2017 presentation, “The Next generation of ISO 11607”, by Nick [...]

Proposed Revisions to ISO 11607 – The Potential Impact on Medical Device Performance Testing 2018-05-10T07:13:26+00:00

Consolidating Your Vendor Network: Why It Is Important To Work With A Laboratory That Offers A Range Of Services

2018-05-10T07:13:26+00:00

Whitehouse Laboratories is one such location that provides all of the testing and validation services that any medical or pharmaceutical manufacturer needs to ensure the efficacy of their products, and the safe delivery to their end use.

Consolidating Your Vendor Network: Why It Is Important To Work With A Laboratory That Offers A Range Of Services 2018-05-10T07:13:26+00:00