Our Blog
The Qualio Blog
Insights on product development, quality management, and regulatory compliance for teams building life-saving products.

How Much Is the FDA Medical Device Registration Fee in 2024?
The FDA medical device user fee for 2022 is $5,672. However, there are other fees medical device manufacturers should be aware of in 2022 and beyond.

Making work even easier for our customers in our November Launch Train
New file formats, faster validation, a brand-new event editing experience and more. Learn how we made Qualio even better in our November 2023 Launch Train!

Top pharma conferences in 2024
Attend the best pharmaceutical conferences in 2024 for pharma industry education and networking opportunities.

The ultimate guide to pharmaceutical quality assurance
Review the scope of quality assurance in the pharmaceutical industry, including responsibilities and expectations of pharma QA teams.

6 strategies for successful biotech funding
Biotech founders use funding strategies like venture capital, grant applications and research partnerships. Learn more about biotech funding strategies.

Understanding the major pharmaceutical regulations you need to know
Review the key pharmaceutical regulations you need to know and understand how they shape quality in the pharmaceutical industry.

I'm Qualio's chief product officer. Here's what the future of our software looks like.
Chief Product Officer Todd Wilkens joined Qualio in 2023 after a string of product leadership roles across the software world. Todd shared his product philosophy and his big plans for Qualio on our blog.

Good distribution practice: understanding GDP compliance
Explore the principles of Good Distribution Practice (GDP) in the pharmaceutical industry, ensuring quality and regulatory compliance in distribution.

How much does ISO 9001 certification cost?
Are you a life science company chasing ISO 9001 certification? Learn all about the cost of getting ISO 9001 certified.