Auditing for QSR Compliance
Date: July 18, 2025
Duration: 60 Minutes
Time: 12 PM EST
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.
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.
- 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.
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.
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
We accept credit card, debit card, and PayPal.
Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
