COVID-19 Resources

The COVID-19 pandemic has introduced unprecedented challenges to the medical device and life-sciences industry. From PPE shortages, remote audits, delays in regulatory processes, and much more. EMMA International has stayed on top of the ever changing quality and regulatory landscape amidst the global public health emergency and has compiled the following resources to keep the life-science industry informed, to ensure life-saving products get to market, and stay on the market.

 

If you need help navigating through COVID-19 for your medical product, EMMA International is ready to help 24/7. Contact us at 248-987-4497 or email info@emmainternational.com to get connected with our team of experts today!

COVID-19 Whitepapers

COVID-19 Articles and Webinars

COVID-19 vaccines have now been approved for a few weeks, and nearly 2 million people in the United States have received their first dose of...

Health Canada released a notice for the stakeholders of the medical device and drug industry to help them understand the tenure of the inter...

Now more than ever, the Emergency Use Authorization (EUA) pathway for medical devices has become a popular topic. Due to the COVID-19 pandem...

As FDA begins to restart on-site inspections of domestic and foreign sites, Health Canada on the other hand has all of its on-site domestic ...

COVID-19 has severely disrupted the medical device supply chain. Device manufacturers are typically not required to report shortages of devi...

The COVID-19 pandemic has had a broad and prevalent impact on the FDA and “normal” medical device life as the industry knows it. Everyth...

Just like every other nation, Australia has also taken several measures to respond to the global pandemic. To help prevent shortages of medi...

The COVID-19 pandemic has caused mass shortages of ventilators and PPE globally, but now healthcare workers are starting to see the effects ...

In our last blog on COVID-19’s impact on the EU MDR, the commission had not yet laid out any intentions of moving the EU MDR deadline, whi...

With the number of confirmed COVID-19 cases now exceeding 200,000 globally, the WHO and many other international government agencies are eit...

With the COVID-19 pandemic halting life as many know it globally, the May 26th EU MDR deadline still looms over the medical device industry....

As the spread of the 2019 Coronavirus Disease (COVID-19) continues to grow globally, the FDA and other global health organizations have had ...