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Why is FDA at my Facility, and What do I do During an Inspection at Riyadh, Saudi Arabia - GlobalCompliancePanel

Event Details

Why is FDA at my Facility, and What do I do During an Inspection at Riyadh, Saudi Arabia - GlobalCompliancePanel

Time: April 20, 2015 at 9am to April 21, 2015 at 6pm
Location: Riyadh, Saudi Arabia
Street: Riyadh, Saudi Arabia
City/Town: Riyadh
Website or Map: https://www.globalcompliancep…
Phone: 18004479407
Event Type: food, fda, medical, device, defence, and, navy, aerospace, mining
Organized By: GlobalCOmpliancePanel
Latest Activity: Feb 19, 2015

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Event Description

Overview:
Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer. This presentation will review and emphasize the do's and don'ts and cardinal rules as to interviewing, how to respond, reviewing documentation, etiquette, use of certain words, body language, responding to questions/requests, etc., and certainly replying to 483's and Warning Letters. Emphasis is placed on the company's SOP on dealing with inspectors and knowing how to be prepared, proactive...and being able to defend and justify... and what it takes to achieve a favorable outcome. This seminar provides background and understanding of the role played by the Agency, its administrative and enforcement powers. It takes the participant step by step through the entire inspection process and describes various types of inspections.

Who Will Benefit:
Industries
  • FDA regulated Industries
    • Medical Device
    • Pharmaceuticals
    • Clinical
  • Dietary Supplements
    • Food
    • Nutraceutical
  • Healthcare IT
    • Technical Services
    • Validation
    • Engineering
Departments
  • Top and Middle Management
  • Quality Assurance/Management
  • Compliance Management
  • Manufacturing
  • Laboratory
  • Regulatory Affairs
  • Information Technology
  • Marketing & Sales
  • Operations
  • Research & Development
Types of facilities:
  • Manufacturing facilities
  • Contract manufacturing facilities
  • Distributors
  • Packaging, Labeling
  • API Suppliers
  • Laboratories
  • Importers
  • Documentation Management

Speaker:

David R. Dills

Regulatory Affairs & Compliance Consultant, 

David R. Dills, Regulatory & Compliance Consultant with more than 24 years of hands-on experience and a proven track record within the FDA regulated industry, has an extensive regulatory and compliance background with Class I/II/III and IVD devices, pharmaceutical operations, and manages activities within the global regulatory and compliance space.
Price: $1,595.00 

Quick Contact:

NetZealous BDA as GlobalCompliancePanel

USA Phone:1-800-447-9407
Fax: 302-288-6884
support@globalcompliancepanel.com
http://www.globalcompliancepanel.com

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