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Life Science Outsourcing Completes Acquisition of J-Pac Medical

Bringing Medical Innovations to Life

Life Science Outsourcing is a performance-driven contract manufacturer helping medical device and pharmaceutical innovators start up, speed up, and scale up.

Your Trusted Partner for Over 25 Years

Life Science Outsourcing has partnered with more than 1,400 medical device innovators to streamline production and navigate complex regulatory requirements. We help innovators successfully enter and expand into new markets and accelerate revenue.

Services and Expertise

Start up. Speed up. Scale up. Founded in 1997, Life Sciences Outsourcing was born of a need to enhance and advance medical innovation. We are an FDA-registered and ISO 13485-certified organization with services and capabilities spanning the entire medical device product life-cycle – from turnkey manufacturing, testing, validation, and sterilization to precision packaging, fulfillment, and distribution.

Each service is purpose-built to deliver proven solutions at the most critical points in the product development process, reducing costs and accelerating time to market.

Medical Device Manufacturing

Innovative assembly, packaging and sterilization. Bringing powerful innovations to life with state-of-the-art medical device manufacturing equipment and assembly expertise that deliver commercially ready devices with unparalleled speed to market.

Medical Package Testing

Packaging design, validation and testing. Delivering superior packaging validation, testing, and design that minimizes costs while ensuring all regulatory requirements are satisfied.

Sterilization & Validation

Contract sterilization and validation services for single use and reusable devices. Providing tailored contract sterilization services for single-use and reusable products that meet all regulations and reporting requirements.

Cleaning & Decontamination

Delivering cleaning and decontamination solutions for reusable medical devices to eliminate bio-hazardous material, meet safety requirements, and ensure necessary certifications.

Fulfillment & Distribution

Ensuring timely and cost-effective logistics and supply chain management services, from warehousing and inventory to packaging and delivery.

Quality Incubator Support

Helping startups and innovators satisfy investor expectations through innovative medical products and accelerated growth.

From Idea to Commercialization

One-Stop Shop

From startups to multinational corporations, we’ve helped pharmaceutical companies and medical device makers of all sizes turn powerful ideas into profitable offerings. Our unique model serves as a turnkey solution offering unparalleled time to market through a full spectrum of regulated services and specialized high-value capabilities.
Deeper Partnership

Agile and Flexible

We act as an external extension of client teams with the depth and expertise to guide, support, and adapt to evolving needs at every turn. With onboarding in as little as one week, our work with clients is rooted in collaboration and shared objectives.

Proven Results

Regulatory Expertise

With decades of hands-on experience, our veteran teams guide clients through the regulatory and commercialization process to mitigate risk, minimize delays and speed up time to market and revenue.

News & Info

Company News

How Do You Speed Up Commercialization Without Compromising Compliance? Visit LSO at OMTEC 2025

Orthopedic OEMs are under growing pressure to move faster without compromising compliance. At OMTEC 2025, LSO will showcase how consolidating packaging, sterilization, and cleanroom assembly under one roof helps eliminate delays and accelerate commercialization. Visit us at Booth 350—or schedule time with our team whether you’re attending or not.
Gas chromatography system used for EO residual testing of sterilized medical devices in a modern laboratory environment.
Sterilization & Validation

What Is Ethylene Oxide (EtO) Residual Testing and Why It Matters for Medical Devices

EtO residual testing ensures that your ethylene oxide sterilized medical device is safe for use and compliant with ISO 10993-7 and FDA requirements. Because patient safety and regulatory submissions depend on accurate chemical residue analysis, EtO residual testing should be a non-negotiable part of your sterilization validation strategy.
A laboratory technician in cleanroom attire conducts a quality control inspection with a clipboard and pen in a sterile facility.
Sterilization & Validation

How Often Should You Perform Bioburden Testing? A Risk-Based Approach

Bioburden testing should never be reduced to a set-it-and-forget-it calendar task. It is a living part of your quality system and a primary indicator of your microbial control status. While quarterly testing is a good starting point for many manufacturers, a truly risk-based program requires ongoing evaluation.

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