Scroll To Top
Search by Speciality

2-day In-person Seminar on “Surviving an FDA Inspection: Understand the Do s and Don ts and the Ground Rules” at Washington DC

Courtyard Washington Capitol Hill/Navy Yard * | Washington dc, USA
From 1295 to 1495 USD
Event Preview
This event
is Finished
Title: 2-day In-person Seminar on “Surviving an FDA Inspection: Understand the Do s and Don ts and the Ground Rules” at Washington DC
Specialty: , Clinical Pharmacology, Internal Medicine, Medical Oncology, Other Specialties, Preventive medicine
Dates: From Oct, 10, 2013 to Oct, 11, 2013
Location: Washington dc, USA
Type: Conference, Congress, Seminar, Workshop
Registration Cost: From 1295 to 1495 USD
Event Tools
  • Add to Favorites
  • Claim this event
Add to my Calendar
  • Scientific Programm
  • Online registration
  • Exhibition floorplans
  • Sponsorship &
    Exhibition consensus
  • Virtual Booths
Weather Info (monthly averages) Max Temperature: C / F Min Temperature: C / F The above data in our Weather Info table are temperature predictions for the date of the medical event for Washington DC, Usa.
General Info
Event Venue:

Courtyard Washington Capitol Hill/Navy Yard *

Washington DC, USA Visit the Venue to read more



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:

This seminar will provide valuable assistance and guidance to all regulated companies that are preparing for FDA inspections.


The employees who will benefit include:

  • All levels of Management for all departments
  • QA/QC/Compliance/Regulatory Affairs
  • Information Technology/Marketing & Sales
  • Engineering/Technical Services/Validation
  • Consultants
  • Operations and Manufacturing

Course Outline:

Day 1 - Agenda

Lecture 1: How a firm should prepare for an FDA inspection 
Lecture 2: Ways to train employees in view of the inspection 
Lecture 3: How to ensure that required documentation is in place 
Lecture 4: How to interact with the investigator-DO's and DON'T's 
Lecture 5: What companies should do when the inspection ends 
Lecture 6: How to reply to 483's and warning letters 
Lecture 7: Legal implications of non-compliance 
Lecture 8: Post inspection actions 

Day 2 – Agenda

Lecture 1: Why inspections are conducted and by what statutory authority 
Lecture 2: The emphasis on systems-based inspections...and the IOM and other crucial FDA reference documents 
Lecture 3: What is subject to FDA purview and what's off-limits 
Lecture 4: Understand and apply the do's and don'ts and comprehend that preparation is the key to success 
Lecture 5: What are the prohibited "Acts" and the enforcement categories that you need to deal with 
Lecture 6: What you need to know and do to prepare for, during and even after the inspection...and why your inspection response team is key 
Lecture 7: The company's Inspection Plan (SOP) can make or break the inspection depending on how to use it and training your personnel 
Lecture 8: How to respond to findings and facilitating the documentation and remediation process...and reaching final closure 
Lecture 9: Define clear responsibilities, roles and goals for personnel involved in SOP development 


About Speaker:

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. He manages quality, regulatory and compliance projects with multiple competing priorities having a direct impact on site operations and commercial opportunities and develops strategies for governmental approval to introduce new products to market, provides guidance on regulatory and compliance requirements and prepares/reviews worldwide submissions/dossiers/technical files and addresses global regulatory requirements.


Date, Venue and Price:

Location:  Washington DC | October 10th & 11th, 2013 | 9 AM to 6 PM

Venue: Courtyard Washington Capitol Hill/Navy Yard

Address: 140 L Street SE, Washington, District of Columbia 20003 USA


Seminar for One Delegate Price: $1,295.00

Register now and save $200. (Early Bird)
Discount: Until September 14, Early Bird Price: $1,295.00 
from September 15 to October 08, Regular Price: $1,495.00

Contact Information

Event Coordinator

Toll free: 1800 447 9407

Fax: 302 288 6884




NetZealous LLC

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA

For More Details:

Event Overview
Registration Not yet available Register Now
Scientific Content Up to Date
Sponsors Exhibitors
Organising Agency

GlobalCompliancePanel is a training source that delivers diverse, high quality regulatory & compliance trainings. These trainings are simple while being relevant and cost-effective while being convenient.

GlobalCompliancePanel imparts knowledge of best practices across a broad range of user-friendly mediums such as webinars, seminars, conferences and tailored, individualized consulting. These help organizations and professionals implement compliance programs that meet regulatory demands and put business processes in place.

GlobalCompliancePanel focuses primarily on providing extensive and quality training in these core areas and anything related to them:

  • Risk Management
  • Regulatory Compliances
  • Corporate Governance
  • Quality Management

Through the mediums by which we offer trainings, namely webinars, seminars, conferences and consulting, we bring together the regulators or experts on regulation on the one hand, with the community that needs to learn or be aware of those regulations, on the other. 

Professionals who undergo trainings from GlobalCompliancePanel exhibit a vastly improved quality of life in which there is increased productivity and professional growth. Some 30,000 professionals have gained from more than 500 training courses we have conducted till now.

In the course of providing world-class training to compliance professionals by compliance and consulting gurus, GlobalCompliancePanel is also:

  • A provider of information to ensure compliance and enhance quality with regulations for individuals as well as the organizations
  • A supplier of the latest updates on industry trends, industry best practices and any modifications in the regulatory affairs
  • A platform for all your queries and to share and discuss issues, ideas and best practices, and
  • A resource on the data sheets, whitepapers, articles, books on industry standards, training kits, software tools, insights, press releases, etc. on governance, regulatory, compliances and quality management across different industries.

NetZealous LLC dba GlobalCompliancePanel is headquartered at 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.

Official Event Webpage
Event map
Revelant Events