Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection training seminars presented by ComplianceOnline register now on FindaSeminar.com

findaseminar logo balls FindaSeminar.com
event search registration and marketing services since 2002
Advanced Search
 
 

** NOTE: All April seminars are live Virtual or Online click to view events.

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection  

 Email information about this seminar Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection by ComplianceOnline to yourself your manager or associates Email this event... View and register for other training seminars like Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection by ComplianceOnline on FindaSeminar.com Find similar training.. Find and register for other training seminars by ComplianceOnline on FindaSeminar.com Other seminars from ComplianceOnline

By:

training seminars by ComplianceOnline ComplianceOnline   

For:

Regulatory Affairs, QA/QCProject Managers, Regulatory Professional, Risk Managers, Complaint Handling Teams, CAPA Teams

Cost:   

see Registration info for seminar cost, group discount etc.

Seminar Summary:

Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas. (see full course description)

 

 Seminar / Training class dates & locations

 

No seminar dates for this event are currently scheduled.  Please use the seminars search box above or choose one of the following additional training search options to find similar training.

medical+device+recalls+regulations+reporting+complaint+management+handling+MDR+CAPA training seminars workshops conferences online training

Providers course catalog

Find seminars by state

Find seminars by city

Request on site training

Use Advanced Search

NEW  Don't miss training you want to attend

Receive a personal Training Alert when training you want to attend comes to your area. Create a personal Training Alert now  it's Free and only takes a minute!


 

 

 

share this page 

print the agenda print agenda for the Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection seminar

 

 

Training Course Syllabus:


Learning Objectives:



  • Understand how to comply with complicated Compliant Handling, MDR and Recall requirements

  • Firms MDR reporting and FDA´s handling of reports

  • Company preparation in the event of a Recall, recall strategy, notification letter and communicating with the FDA

  • Minimize your risk of regulatory enforcement actions

  • Assist with the creation and maintenance of effective procedures for handling complaints, reportable events and recalls

  • Understand the relationship and interaction with other quality system elements as they relate to complaints and reportable events

  • Walk-through of case examples

  • Step-By-Step guide to designing Standard Operating Systems for communicating process for firm’s success

  • Discussion of FDA’s New Guidance’s on Risk and how it interacts with Recalls


Seminar Summary:

Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas. (see full course description)

print this agenda print agenda for the Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection training seminar

 view dates and locations for this seminar

 

 

 

Custom Search