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Medical Device Safety & Reporting Summit 2019

March 25 @ 8:00 am - March 26 @ 3:45 pm

 

Medical Device Safety & Reporting Summit

At the Medical Device Safety & Reporting Summit, industry professionals will gather to further enhance the knowledge surrounding the importance to maintain the quality of your medical device and ensure valuable risk management plans to pace ahead of the competition without having any setbacks. With medical device safety playing a critical role in healthcare, it is significant for organizations to ensure effectiveness by implementing a safety action plan to ensure success for the product.

Whether it is an oxygen mask, nebulizer, cardiovascular stent, medical imaging equipment, or robotics, there are certain requirements that each device must meet before going to market. While these medical devices are paramount when providing care to patients, they occasionally fail to operate OR are misused causing further harm to the patient or even death, which makes risk assessment an important juncture when developing a medical device. This event will go through in-depth details and properly arm you wish successful strategies in order to enhance product development to maintain leverage in the marketplace.

 

Featured Speakers

 

 

Top Five Reasons to Attend

  1. Ensure medical devices meet proper regulatory requirements and the highest quality standards
  2. Benchmark best practices and guidelines for medical device monitoring and safety with a post-approval surveillance strategy
  3. Recognize future regulation implications and ensure a successful risk management plan
  4. Allow patients to access high-quality devices with innovative strategies to maintain compliance with the FDA
  5. Essential elements of an effective corrective and preventive action (CAPA) system while maintaining compliance with reporting and documentation processes to avoid regulatory issues

 

Who Should Attend

  • Quality Management
  • Clinical Quality Management
  • Quality Assurance
  • Regulatory Affairs
  • Medical Affairs
  • Medical Device
  • Risk Assessment
  • Compliance/Ethics
  • Monitoring
  • Site Management
  • Site Quality
  • Research and Development
  • Project Management
  • Pharmacovigilance
  • Safety
  • Data Management
  • Real-World Evidence
  • Adverse Events/Case Management Service Providers
  • Safety Database Providers

 

This conference is also of interest to:

  • Healthcare/Pharmacovigilance Consultants
  • Technology Vendors
  • CROs

 

 

To register, please clikch here

 

Details

Start:
March 25 @ 8:00 am
End:
March 26 @ 3:45 pm
Website:
https://exlevents.com/medical-device-safety-reporting

Venue

The Inn at Penn, A Hilton Hotel
3600 Sansom Street
Philadelphia, PA 19104 United States
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Organizer

ExL Events
Phone:
For information on speaking opportunities, please contact Warren Drysdale at wdrysdale@exlevents.com or 917-258-5162.
Email:
For information on sponsorship or exhibition opportunities, please contact Jayson Mercado at jmercado@exlevents.com or 212-400-6236.
Website:
http://exlevents.com