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.

Areas Covered

•    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
•    Preparation
•    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;
•   Engineering;
•   Manufacturing;
•   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.

Speaker Profile

Jeff Kasoff

FDA Speaker, Quality and Regulatory Consultant

Jeff Kasoff has also been primary liaison with FDA inspectors and notified body auditors, giving him first-hand experience with the most common issues surfaced by regulatory agencies. Jeff received his Regulatory Affairs Certification from RAPS, his Manager of Quality and Organizational Excellence certification from ASQ, and his Lean Black Belt from IIE.

Jeff Kasoff, RAC, CMQ/OE has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operations and assured compliance, at all sizes of company, from start-up to more than $100 million in revenue. This multi-faceted experience makes Jeff uniquely qualified to address compliance issues across the entire range of company sizes.

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