COVID-19

Navigating Together for a Better Tomorrow


How Quasar Is Responding to COVID-19 and Its Effect On Businesses

As the coronavirus pandemic continues to change the world, we’re all navigating through uncertainty. 

At Quasar, we embrace our “philosophy of operational excellence”. This means that even in times of struggle, we have an operational focused effort. While our number one concern is the health and safety of our employees and our community, we are also here to assist you with business continuity, even in these uncertain times.

Covid-19 resilience

How We're Helping

Meeting all Q-2 commitments and more.

We are here to support the medical device companies globally who have been affected by the pandemic and thus facing challenges to meet previously set production goals. To ensure we are in a position to to support your production needs, we have EXPANDED Manufacturing Capacity in the following areas:

ISO/FDA Registered Facilities

+30k sqft ISO 7/8 Clean Rooms at our ISO/FDA Registered Facilities in China, Hong Kong, and Thailand.

Fully staffed

with additional capacity to support Class II & III devices.

Critical Backorders recovery plan

Commercial and Manufacturing teams at the ready to assist with evaluating and developing a recovery plan for you.

Second Source

Commercial, Quality and Supply Chain teams at the ready to assist with your supplier qualification and approval process to qualify a second source.

Manufacturing Transfers

Commercial, Quality and Engineering teams at the ready to assist with validation and transfer plans to support a manufacturing transfer project.

Emergency Action Plans

Quasar can assist with developing an emergency (mitigation) action plan to avoid future disruptions to your supply chain.

CONTACT US


COVID-19 Resources

post-market surveillance medical device

Post-Market Surveillance for a Medical Device: What You Need to Know

In addition to the regulatory requirement, post-market surveillance offers an opportunity for collecting market data that can provide valuable insight into the device improvement. In this article, we cover some of the tremendous value that can be created both on the business side and the engineering side when post-market surveillance is done correctly for your medical device.

post-market surveillance medical device

Post-Market Surveillance for a Medical Device: What You Need to Know

In addition to the regulatory requirement, post-market surveillance offers an opportunity for collecting market data that can provide valuable... read more

change control

How to Create an Efficient Change Control Board Process

We rely on these best practices for the most efficient change control board process. This ensures that the medical... read more

Covid-19 resilience

COVID-19 Case Study: A Demonstration of Resilience and Operational Excellence

How Quasar was able to ensure the safe return of over 1,300 employees with zero cases of infection found... read more