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4th Annual ComplianceOnline Medical Device Summit 2018 - Seminar in San Francisco, California, United States on June 2018 by Compliance Online. Medical Device Summit 2018, San Francisco, CA, Seminars, Events & Conferences.

Seminar Information

4th Annual ComplianceOnline Medical Device Summit 2018

4th Annual ComplianceOnline Medical Device Summit 2018, San Francisco, California, United States
Seminar Title
4th Annual ComplianceOnline Medical Device Summit 2018
Event Type
Seminar Date
07-06-2018 to 08-06-2018
Last Date for Applying
San Francisco, California, United States

Publish / Maintain / Marketing / Hosted By
Organization Name / Organize By
Organizing/Related Departments
Medical Device
Organization Type
Event Organizing Company
Seminar Category
Seminar Level
All (State/Province/Region, National & International)
Related Industries



San Francisco, California, United States

Key Attraction
Innovate novel ideas for advancements in medical device technologies without compromising their safety and effectiveness. This summit brings together some of the renowned R&D experts and technology innovators to share information regarding opportunities, obstacles, best practices and challenges in the development of the new devices. Attendees will get insight into device innovation trends and upcoming changes in the medical device regulations.
Plan for successfully executing regulatory inspections by providing industry best practices. Panel discussions led by the former FDA office bearers and industry experts will provide a set of comprehensive strategies on how to prepare for and manage an FDA inspection, including how to follow-up and closing out 483s or Warning Letters. Attending this summit will enable you to improve and better prepare for your next inspections.
Build FDA compliant quality management systems. Attend this summit to learn how to develop and implement effective, consistent and reliable quality management systems. Ex-FDA officials and senior company executives will share thoughts and ideas to improve the performance of your current system.
Interact with leading minds in the industry. Attendees will get to network with the prominent decision makers in the industry to exchange ideas, offer thoughts and know-how, and share experiences. Joining this summit will offer a unique opportunity to the attendees to market their offerings and identify new business opportunities.
Deliberate the current state of medical device laws and technology and government oversight. Panel comprising of some of leading medical device experts and veterans will discuss the recent changes to the regulatory environment for the medical device industry and how these changes will impact the approval of new devices. Attendees will gain insight into the current issues and future challenges in the industry. Join this summit to hear from the experts who have extensive experience in all aspects of medical device including R&D, manufacturing quality assurance, approval and commercialization process.
Scale factors for successful medical device commercialization. Discussions with industry veterans through real case studies will help medical researchers, healthcare professionals, industrialists and entrepreneurs better understand the criterias for successful commercialization of medical devices. This summit also offers numerous opportunities for medical device companies and suppliers to showcase their products and services to potential customers, generating leads and growing their businesses.
Enhance risk management strategies for the safe, effective and efficient use of medical devices. Medical device professionals will join together to share their knowledge and best practices for implementing good risk management principles within the industry. Attending this summit will help you to develop a robust and integrated risk management plan to improve quality management system.

Why you should attend this summit

  • Future Trends of Medical Device Regulation, Risk Management, UDI, Recall Complaint Management etc.
  • Listen from FDA/CDRH Directors:
  • What is Critical to Quality
  • Get Update on FDA compliance

Listen from FBI:

  • Cyber Security Risks
  • Learn More about Medical Device Global Regulatory Landscape and Off-label Promotion
  • Explore Upcoming Changes in Medical Devices under Trump Administration
  • Change Management
  • Criteria for Supplier Quality Agreement
  • Establishing a Medical Device Security Program
  • Panel Discussion
  • FDA Warning Letter
  • FDA Enforcement
  • FDA Interaction

Note: Use coupon code REFERRAL10 and get 10% off on registration.

For Registration:

Registration Fees
Registration Fees Details
Seminar for One Registration - 999
Registration Ways
Omni San Francisco Hotel 500 California Street, San Francisco, CA  Pin/Zip Code : 94104

2479 East Bayshore Road Suite 200, Palo Alto, CA, USA