Online Training 2015 - Best Practices to Prepare for and Manage Compliance Audits by EU Notified Body and FDA - By Compliance Global Inc
Date2015-05-28
Deadline2015-05-28
VenueCompliance Global Inc. 2754 80th Avenue, New Hyde Park, NY 11040, USA - United States
KeywordsMedical device reporting train; Medical device regulations; Fda medical device
Topics/Call fo Papers
Overview:
This webinar is intended to help you get familiar with compliance audits by the US Food and Drug Administration and Notified Bodies in European Union (EU).
This webinar is further intended to help you understand what you can do to best prepare for and manage the audits by EU Notified Bodies and FDA with increased awareness.
The FDA enforcement actions have recently increased. In EU, EU commission issued recommendation concerning unannounced audits by notified bodies in medical device industry.
As a medical device firm, you are subject to regulatory audits or inspection by the US FDA and EU notified body if you bring your medical device products into the US and EU countries allowing CE-marked products.
This webinar will cover the details of how you can proactively prepare for and manage the audits.
Why Should You Attend:
? To learn how to adequately prepare for and manage regulatory audits by the US FDA and EU notified bodies.
Areas Covered in the Session:
? Laws and Regulations: US and EU
? Definitions
? EU Unannounced Audits
? Overview of both ISO 13485 and FDA 21 CFR 820
? Understanding Auditing Strategy
? Audit Objectives and Process
? Auditing Quality Management Systems
? Internal Audit Programs
? Quality Systems and Subsystems in ISO 13485 and under 21 CFR Part 820
? FDA and ISO 13485 training
? Common Mistakes/Misconception: How to Avoid Them
? Communication during Audit or Inspection: Dos and Don’ts
? Good Practices: Dos and Don’ts
? Conclusion
Learning Objectives:
This webinar will cover the details of how you can proactively prepare for and manage the audits.
Who Will Benefit:
? Regulatory Affairs Consultants
? Quality Site Professionals
? R&D Professionals
? Complaint And Risk Management Personnel
? Consultants
? Contractors/Subcontractors
? CEOs
? VPs
? Clinical Affairs Consultants
? Other Interested Parties
Level:
Intermediate
For more detail please click on this below link
https://www.complianceglobal.us/product/700081
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
This webinar is intended to help you get familiar with compliance audits by the US Food and Drug Administration and Notified Bodies in European Union (EU).
This webinar is further intended to help you understand what you can do to best prepare for and manage the audits by EU Notified Bodies and FDA with increased awareness.
The FDA enforcement actions have recently increased. In EU, EU commission issued recommendation concerning unannounced audits by notified bodies in medical device industry.
As a medical device firm, you are subject to regulatory audits or inspection by the US FDA and EU notified body if you bring your medical device products into the US and EU countries allowing CE-marked products.
This webinar will cover the details of how you can proactively prepare for and manage the audits.
Why Should You Attend:
? To learn how to adequately prepare for and manage regulatory audits by the US FDA and EU notified bodies.
Areas Covered in the Session:
? Laws and Regulations: US and EU
? Definitions
? EU Unannounced Audits
? Overview of both ISO 13485 and FDA 21 CFR 820
? Understanding Auditing Strategy
? Audit Objectives and Process
? Auditing Quality Management Systems
? Internal Audit Programs
? Quality Systems and Subsystems in ISO 13485 and under 21 CFR Part 820
? FDA and ISO 13485 training
? Common Mistakes/Misconception: How to Avoid Them
? Communication during Audit or Inspection: Dos and Don’ts
? Good Practices: Dos and Don’ts
? Conclusion
Learning Objectives:
This webinar will cover the details of how you can proactively prepare for and manage the audits.
Who Will Benefit:
? Regulatory Affairs Consultants
? Quality Site Professionals
? R&D Professionals
? Complaint And Risk Management Personnel
? Consultants
? Contractors/Subcontractors
? CEOs
? VPs
? Clinical Affairs Consultants
? Other Interested Parties
Level:
Intermediate
For more detail please click on this below link
https://www.complianceglobal.us/product/700081
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
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Last modified: 2015-03-19 14:58:24