Addressing Challenges in Primary Packaging Testing for Medical Devices

Developing and evaluating primary packaging for medical devices continues to be an area ripe for innovation, with ample opportunity to improve existing processes. Read on to learn more about the topic.

Enabling CDMO Success Through Intelligent Testing Capabilities

While mechanical testing may play a small role in the total scope of CDMO competencies, a poorly equipped solution can result in significant issues with time management, data integrity, and root cause analysis. Investing in highly capable testing systems should be considered a long-term investment and serve to showcase a commitment to quality for potential clients. Read on to learn more.

Packaging and Processing: Life Sciences Industry Strives to Become More Sustainable

The pharmaceutical industry’s pivot toward sustainability reflects a broader movement in global business practices where environmental responsibility is not just a choice but a business imperative. Read on to learn more.

Medical Packaging: Automation of Thermoforming Processes

The medical packaging market has quickly embraced the use of automation for the thermoforming process. Automation has enabled adherence to stringent quality requirements and has...

Medical Plastics: Understanding Ultrasonic Welding, Part 1

Plastic consumables for medical applications are often very complex and sophisticated devices. Before these devices can be used by healthcare workers or home care patients, they...

Medical Device Package Testing: Developing a Test Plan that Avoids Product Launch Delays

Engineers are thinking of creative ways to design a packaging system that will ensure safe arrival of a medical device.

Low Latency Manufacturing for Biophotonics and Medical Device Packaging

Machine-to-machine communication, deep learning, XR, and AI are all going to have an extraordinary will require low-latency manufacturing.

Guide to Package Integrity & Validation Testing under ISO 11607 and MDR

Updates to ISO 11607, Parts 1 and 2, have left many medical device manufacturers wondering about the future of their packaging designs. These changes come at a stressful...

Reimagining Innovation: Additive Manufacturing

In the injectable drug-delivery industry, expectations for improved patient experiences with administration and at-home delivery of therapeutic regimens are evolving. Products that combine the...

Package Engineering for Sterilization

After years of research and development, surveys and polls, functional device testing, and countless other preparatory actions, your medical device is almost ready to go to market. You have determined your...

A Multilayered Approach to Extruded Tubing

Along with cost savings, coextrusion technology offers improved functionality in new tubing products. This article explores how this micro-dimensional tubing is currently being used to meet...

Current Trends in Sterile Medical Packaging and How They’re Impacting OEMs

The medical device industry often gets attention for its innovation and constant evolution. However, even the most innovative medical device technology is of no use if...

Ensuring Your Medical Device Meets Sterilization Standards Throughout the Supply Chain

Ensuring that device packaging meets specifications. Considering the complex science and research that goes into developing medical devices, it is important...

Engineering and Construction Process for Custom Device Cases

When bringing new medical equipment or portable mobile medical devices to market, manufacturers turn to packaging engineers to develop custom case solutions that can enhance and...

Making the Right Choice for Primary Packaging

Technipaq, Inc., Crystal Lake, IL At the onset of a project it seems there are a myriad of things that an engineer or packaging professional should consider when choosing an effective material...

Top Challenges for Today's Medical Device Designers: Winning the Space Race

The phrase, "May you live in interesting times" certainly applies to today's medical device design engineers, as they face unprecedented opportunities and challenges...

The FDA’s UDI Rule is Final: What’s Next?

The U.S. Food and Drug Administration (FDA) published the final rule for the unique device identification system (UDI) during the UDI Conference in Baltimore, MD, and released it on September 24,...

Eight Things to Look for in a Medical Device EMS Provider

Today’s medical device OEMs live in an age of abundance: both abundant options and abundant regulatory requirements. With so many options and so many restrictions, it can be very...

Passive Thermal Management Options for EMS Devices

High-frequency pulsed electromagnetic stimulation (EMS) devices are more powerful and effective than ever before. These devices are finding applications in many areas, including as treatments...

Multilayer Construction Offers Functionality and Versatility

The medical area has long required specialized materials be utilized to treat patients, and the processes of drug delivery and fluid handling are no exception. Hospitals across the...

Advances in Polycarbonate Color Compensation Technology to Withstand Sterilization by Irradiation Methods

Single- and multiple-use medical devices typically require sterilization prior to their use in order to provide for patient safety....

Pre-Validated Medical Packaging Solution

Due to the complex requirements of the medical device industry, the internal resources of device OEMs are drawn primarily to the device R&D and regulatory arenas. However, once the device R&D is...

Medical Device Packaging Validation Testing 101

Package validation testing has always been an important aspect of many medical device development processes. Today, it isn’t just new packaging that manufacturers need to worry about —...

Get an Early Start on a Successful Packaging Solution

The packaging system is a crucial component to getting a medical device to market on time. Time constraints with new projects can affect the packaging system and may prohibit a proper...

Medical Device Testing: Start With a Strategy and Plan

Most medical device manufacturers must first receive approval from the U.S. Food and Drug Administration (FDA) before they can market a medical device. Device manufacturers must demonstrate...

Implantable Microsystems for Anatomical Rewiring of Brain Circuitry

It has been demonstrated that after a stroke-like lesion in the cerebral cortex of non-human primates, the remaining intact tissue undergoes extensive neuro-physiological and...

Exact Dose Dispensing Closure for Semi-Solids

A novel closure technology now makes it possible to consistently squeeze an exact dose of semi-solids from a tube by means of a 180-degree rotating closure. It has potential uses in pharmaceutical...