The FDA Inspection: From SOP to 483
01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute
Webinar Includes : All the training handouts , Certificate by the Speaker ,Q/A and 60 Min Live Webinar
"Hear By Jeff Kasoff, RAC, CMQ/OE has more than 30 years in Quality and Regulatory management"
This is a detailed course designed to provide medical device/pharmaceutical professionals with the information they require to prepare for and manage FDA inspections
This course provides the rationale, strategies and flow on how to plan for an inspection, the inspection process and approach, and which company roles should be assigned for these types of inspections, among other related topics.
Why one should attend the training
The FDA inspection is the most nerve-wracking event in the life of a regulatory professional - you're in charge of compliance, usually in the background, and NOW you're in the spotlight, and if your performance isn't good, it's not the show that may close, it's YOUR COMPANY! However, adequate planning, training, composure, and understanding should result in many encore presentations! This session will discuss how to prepare for the inspection, what to do during the inspection and the close-out interview, and how to respond to the inspection. Also contained in this session will be the limits of FDA's scope during an inspection, including what documents you are not required to show them, and the permissibility of photographs and affidavits.
• Does the FDA call in advance or just show up at my door?
• Where do I let the inspector go?
• Do I give them a tour?
• What should I let them see?
• Who should I let them talk to?
• Are they ever going to leave?
Key learning objectives of the Topic
• Types of Inspections
• Dedicated personnel for inspection
• Facility resources to support the inspection
• Internal audits
• Mock audits
• SOP for inspections
• Behavior during inspection-what to say, what not to say
• Inspection process
• 483 response process
Who will Benefit
• Quality Auditors
• Compliance Officers
• Executive Management
• Managers/Directors/Supervisors and Personnel related to:
• Regulatory Compliance and Regulatory Affairs;
• Quality Management System;
• Quality Assurance;
• Quality Control;
• Product Development;
• Risk Management;
• Complaint Handling
• Personnel new to the regulated industry
• Training personnel
• Document Control Personnel
Industries who can attend
This 60-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.