News & Insights

The Strategic Advantages of Localized Ethylene Oxide Sterilization Services for Medical Devices

Localized small batch EtO sterilization can help you avoid backlogs and costly delays associated with large batch ethylene oxide sterilization processes. Learn more.

The Art and Science of Custom Microfluidic Blister and Cartridge Packaging Design

Custom package design requires compliance, usability, and microfluidic stability. OEMs should consider these and more when ready to take the next packaging step.

Unveiling the Vital Role of the Sterile Barrier in Medical Device Packaging

Medical device manufacturing involves a rigorous process to maintain patient safety and prevent infections. Medical package design and its sterile barrier play a critical role.

Using Contract Manufacturer Facilities and In-House Services Expedites Medtech Time to Market and Reduces Risk

Medical device startups need clean rooms and equipment to fast-track new products to market. The right contract manufacturing partner can help.

How Can Medical Device Companies Achieve Sustainable Scalability for Long-Term Growth?

Medical device product scalability isn’t just about making more product – it’s about long-term capabilities, resources, and infrastructure. Learn more.

Unpacking Success: Medical Device Packaging Checklist for Successful Product Launches

Package design is critical to a new medical device product launch. Avoid costly delays and better understand the process with our medical device packaging checklist.

6 Methods for Medical Package Sterile Barrier Validation Testing: INFOGRAPHIC

Is your medical device packaging leak-free and secure from outside contaminants? Validation testing minimizes package failure risk and meet ISO regulations.

LSO Welcomes Yiorgos Polizos as Vice President of Sales & Marketing

Life Science Outsourcing, Inc. appoints Yiorgos Polizos as VP of Sales & Marketing, leveraging his vast experience to drive growth & innovation in medical device outsourcing.

The Right Challenge Device for Ethylene Oxide (EO) Sterilization Validation

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.

7 Industry Recommended Best Practices for Medical Device Sterilization: Infographic

Design Terminally Sterile Packaging 3 Ways to Prevent ISO 11607 Package Design Failure (Infographic)

LSO Employees delivered outstanding results in the most difficult circumstances

There’s no question that 2021 was challenging. LSO Employees delivered outstanding results in the most difficult circumstances.