Watch our RAQA Deep Dive session featuring Nicholas Wells, an expert in regulatory strategy and intelligence, as he shares actionable...

Navigating the complexities of adverse event monitoring can be challenging. With data coming from diverse sources—like regulatory...

We are thrilled to announce that all of our webinars from the past year have finally found a home! Our Webinar Gallery is now live,...

In an era where efficiency and precision are paramount, effective reporting is essential. Did you know that automating the reporting,...

The landscape of medical device regulations and standards is evolving rapidly, with an increased emphasis on surveillance and vigilance....

Artificial Intelligence (AI) has become an integral part of our daily lives, influencing everything from the way we communicate to how we...

Hope you're having a great summer! 🌞 As the landscape of medical device regulations continues to evolve, so does the emphasis on...

Finding time to relax and recharge is essential. Reading can be a great way to unwind while also enriching your professional knowledge. We asked 20 of our RAQA friends for tips on books to read during their vacations. Let us present the top 5 mentioned books and another 5 as additional picks. Whether you’re on a sunny beach or in a winter snow land , these books offer valuable insights that can enhance your professional life in RA and QA. Enjoy your reading, and with Hoodin b

We're thrilled to share our brand new series designed to provide you with the latest features, tools, and insights in the realm of surveilla

The Power of Social Media for Vigilance and Adverse Event Monitoring

The landscape of Regulatory Affairs and Quality Assurance (RAQA) in life sciences is complex, fast-evolving, and crucial for maintaining...

Post-Market Surveillance (PMS) is a critical aspect of ensuring the safety and efficacy of medical devices after they are placed on the...

Welcome to the Hoodin RAQA Deep Dive Sessions post! In this edition, we'll explore insights from our recent special edition webinar where...

In today's rapidly accelerating intelligence and information landscape, the role of Artificial Intelligence (AI) in regulatory affairs is...

Attention all industry professionals, the moment has finally arrived! After months of anticipation and hard work behind the scenes, we are

Dive into the intricate world of regulatory classifications with Veronika Valdova as she shares real-world examples of medical devices that

In the world of regulatory affairs, effective communication and teamwork are vital for successful surveillance. Neglecting these crucial...

Keeping up with the latest regulations and best practices for post market surveillance  medical devices and In Vitro Diagnostics (IVD) is...

Dear Reader, We are delighted to invite you to our upcoming webinar, "Collaboration is Key: Leveraging Teamwork for Enhanced...

Welcome to the Hoodin RAQA Deep Dive Sessions Recording & Resources page! Here we'll explore insights from our recent session with...