News & Information

Michael Dizon has been promoted to the position of Human Resources Director. He joined LSO in 2018 and has earned this promotion through his continued hard work, dedication, and successes as LSO’s HR Manager.

In the last 25 years, Life Science Outsourcing, Inc. has become a leading medical device contract manufacturer for start-ups, global organizations, and everything in between. How did it start, and what’s in store for the future?

Packaging, Sterilization Considerations Go Part and Parcel with Product Development – LSO featured on cover and main article of MPO Magazine

The European Union Medical Device Directive (EU MDR) will impact medical devices and medical package testing for products in the European market.

Ethylene oxide sterilization (EtO) has been a reliable medical device sterilization practice for many years. How does it impact the environment and technicians?

When does medical package testing require a protocol? What exactly is involved? Read the answers here, along with why a proper written and approved protocol should always be considered.

Ethylene oxide (EtO) sterilization for gas-compatible medical devices is a much sought-after process for terminal sterilization and sterilization of reusable devices. For some devices, it is the only sterilization method that is effective and will not damage the device. But how is it tested and validated? Biological indicators along with external process challenge devices are a key part of the process.

What is dunnage and what does it have to do with medical package testing? Find out in our latest article which details the ways dunnage can reduce medical package testing costs without derailing regulatory approvals.