Webinars>>FDA Audit
Auditing for QSR Compliance

Are you a medical device manufacturer looking to stay ahead of the curve and ensure your products meet the highest quality standards? The FDA's Quality System (QS) Regulation has been the cornerstone of the industry for over two decades, but times have changed, and regulatory expectations have evolved. It's time to equip yourself with the latest knowledge and align your Quality Management System (QMS) with internationally recognized standards.
 
Introducing our exclusive seminar on Auditing for QSR Compliance! This is a unique opportunity to learn from industry experts and gain invaluable insights that will take your business to new heights of success.
 
Why should I attend:

1. Stay Compliant with Evolving Regulations: Regulatory authorities worldwide are moving towards harmonization of Quality Management System (QMS) requirements. Our seminar will provide you with an in-depth understanding of how the FDA is aligning the QS Regulation with ISO 13485, the internationally accepted standard. By staying ahead of these changes, you'll ensure your devices meet global compliance standards, opening up new markets and opportunities.
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2. Maximize Flexibility in Your Manufacturing Processes: Every medical device is unique, and manufacturers must have the flexibility to tailor their processes accordingly. Our seminar will guide you on how to navigate the QS Regulation and establish requirements specific to each type or family of devices, resulting in safe, effective, and top-notch products. Take control of your production processes and enhance overall efficiency.
3. Know Your Applicability: Not all medical device manufacturers are subject to the same regulations. Our expert will help you understand the scope and applicability of the QS Regulation, ensuring you focus on the areas that matter most to your business. Don't waste time and resources on unnecessary compliance measures; invest in the knowledge that matters!
4. Discover GMP Exemptions: FDA has identified certain medical devices that are exempt from Good Manufacturing Practice (GMP) requirements. Our seminar will clarify which devices fall under these exemptions, saving you valuable time and resources while ensuring you maintain compliance where it counts.
Who will benefit: 
  • Regulatory Affairs Professionals
  • Quality Assurance Professionals
  • Medical Device Manufacturing Professionals
  • Senior Management Executives (CEO, COO, CFO, etc)
  • Clinical Trial Managers
  • Directors and Project Managers
  • Regulatory Compliance Associates and Managers​
  • Documentation Management Personnel
  • Project Managers and Clinical trial specialists
  • Pharmaceutical and Biotech Industry Professionals involved in clinical trial planning and execution.
Date: May 14, 2024
Time: 12 PM EST
​Duration: 60 Minutes

Speaker Mukesh Kumar
​PhD, RAC | Brij Strategic Consultations,  USA

    For more info, fill the box below. We will contact you within 24 hrs.
Don't miss out on this game-changing opportunity to elevate your business. Sign up for our Auditing for QSR Compliance Seminar and take the first step toward ensuring your medical devices meet the highest quality standards and regulatory expectations.
 
Space is limited, so reserve your seat now and unlock your business's full potential! Together, we'll pave the way for a successful future in the medical device industry.
 
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: [email protected]