Health Canada has unveiled its Forward Regulatory Plan for 2024-2026, outlining significant amendments to the Natural Health Products Regulations and the Food and Drug Regulations under the Food and Drugs Act. These amendments are designed to align the regulatory approach for self-care products, ensuring a streamlined and risk-based framework that reflects contemporary standards. To better understand the proposed amendment, it’s essential to first understand Natural Health Products (NHPs) and Non-Prescription Drugs.
Recent Updates
  • What Is a Critical Control Point in HACCP and Why It Matters
    When it comes to food safety, having a reliable and preventive system in place is essential. That’s where the HACCP (Hazard Analysis and Critical Control Points) system comes in—a globally recognized method for identifying and managing food safety risks. At the heart of this system lies a crucial concept: the critical control point. But exactly what is a critical control point, and...
    0 Comments 0 Shares

  • 510k Submissions | Medical Device Registration
    Submitting a 510(k) application to the FDA for your medical device can be a stressful and complicated process. Luckily, there are a few tips and tricks you can use to make the submission process easier and increase the likelihood of your device being approved.

    Get assistance with medical device 510(k) premarket submissions from an FDA expert at Quality Smart Solutions. Are you looking for an FDA 510(k) consultant? You’ve come to the right place! We have years of experience helping companies navigate the process of obtaining regulatory clearance for their medical devices.
    Read More - https://qualitysmartsolutions.com/510k-medical-device-registration/
    510k Submissions | Medical Device Registration Submitting a 510(k) application to the FDA for your medical device can be a stressful and complicated process. Luckily, there are a few tips and tricks you can use to make the submission process easier and increase the likelihood of your device being approved. Get assistance with medical device 510(k) premarket submissions from an FDA expert at Quality Smart Solutions. Are you looking for an FDA 510(k) consultant? You’ve come to the right place! We have years of experience helping companies navigate the process of obtaining regulatory clearance for their medical devices. Read More - https://qualitysmartsolutions.com/510k-medical-device-registration/
    510(k) MEDICAL DEVICE REGISTRATION
    0 Comments 0 Shares
  • 0 Comments 0 Shares
More Stories