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

Meeting the stringent new CE mark recertification MDR requirements will take time, planning, and expertise. This is what you need to know to get started.
Medical Device Manufacturing

What do Medical Device OEMs Need to Know for MDR CE Mark Recertification in Europe?

The medical device industry is only a few years away from the MDD becoming the MDR for CE mark recertification in Europe. On average, it takes 18 months to recertify medical devices – meaning that slower-to-adopt companies may fall behind and risk losing certification altogether.
Life Science Outsourcing offers steam sterilization.
Sterilization & Validation

Steam Sterilization for Medical Devices: How it Works, ISO 17665, and Comparison to Other Methods

Steam sterilization is a popular medical device sterilization method that many manufacturers use to successfully prepare their devices for market and meet industry regulation standards. But is it right for your device? Learn how it works, the ISO industry standards, which devices are ideal for this sterilization method, and how it compares to other sterilization options available on the market today.
Medical Device Manufacturing

3 Requirements for Reliable Manufacturing Supply Chain Continuity

Medical device companies have a real challenge when managing diverse supply chain demands, especially if they utilize multiple resources to achieve disparate processes. And it’s no surprise that difficulties will continue to arise as we move into 2024 in the form of new requirements, resource access limitations, a lack of in-house expertise, and disconnected communication channels.