Medical Device Assembly & Packaging White Papers

Validating Medical Device Assembly, Packaging, & Sterilization

by: J-Pac Medical

Validating Medical Device Assembly, Packaging, & Sterilization

Introduction

According to the World Health Organization (WHO), healthcare-associated infections (HAIs) are the most frequent adverse event in the delivery of healthcare services worldwide. Ensuring the sterility of medical devices is a critical step in the overall effort to reduce the rate of infections in hospitals and other healthcare settings.

Establishing Shelf Life of Medical Devices

by: J-Pac Medical

Establishing Shelf Life of Medical Devices

Introduction

Determining a medical device’s shelf life can be one of the more challenging aspects of a new device development program. Manufacturers must account for internal (component interactions and material degradation) and external (manufacturing, sterilization, shipping and storage) variables that will influence shelf life claims. These claims are developed via rigorous testing. An ideal shelf life testing strategy is proposed.

How Pre-Validated Medical Device Packaging Complies with ISO Standards

by: J-Pac Medical

How Pre-Validated Medical Device Packaging Complies with ISO Standards

Introduction

There is a lot of excitement in the medical device packaging industry about pre-validated packaging. Using pre-validated packaging may reduce time to market and minimize expense related to package development and validation.

Product Sheets

Download the details you need about Medical Device Assembly & Packaging products and services from J-Pac Medical.

Latest News

May 20, 2021


Breaking down barriers to scale up medical device manufacturing

Explore our Photo Gallery

See examples of our medical device outsourcing products and services

Call Our Engineers Now

603.692.9955

info@j-pacmedical.com