Two Day Seminar: Managing Your FDA Inspection: Before, During and After (San Diego, CA, United States - June 15-16, 2017) - Research and Markets

DUBLIN--()--Research and Markets has announced the addition of the "Managing Your FDA Inspection: Before, During and After" conference to their offering.

FDA inspects many different kinds of firms. If the FDA regulates your product, they can show up at your lobby and say, I am here to conduct an inspection. What do you do? What have you done to prepare for an inspection? How do you deal with the investigator, including their personality? The scary part is having to explain the error of your ways to the FDA and above all, managing an administrative action, e.g., Warning Letter or Import Alert, or a legal action, e.g., civil money penalties, seizure, injunction or prosecution. This course will help you need to know and what you should do to survive an FDA inspection with the least possible pain.

Seminar Instructor Casper Uldriks is an "Ex-FDA Official" who has spent 32 years in FDA. He currently trains FDA personnel and counsels clients on wide range of topics, including: FDA inspections; import operations; advertising and promotion; corrective and preventive actions; medical device reporting and corporate reorganization to improve conformance to the FDA's requirements.

The course will cover the factors used by the FDA to schedule inspections. You will learn how to predict what an FDA investigator will do and what they will cover in the inspection. There should be no surprises if you have prepared properly. Firms need to understand the details about inspectional techniques to avoid making new problems for yourself during the inspection. You can save yourself a lot of corporate misery if you know what to do before, during and after an inspection.

Learning Objectives:

- FDA legal authority to inspect

- Over products

- Over firm's

- Scientific/clinical studies

- Premarket requirements

- Postmarket requirements

- FDA's annual inspection work plan

- Inspection Procedures

- FDA inspection Manuals

- FDA Training

- Documenting violations

- Refusals

- Human factors

- Recall procedures (What FDA expects from you.)

- FDA Field Office Management

- FDA Center(s) Management

- The firm's job

- Inspectional observations (Form FDA-483)

- Responding to a 483

- Responding to a Warning Letter

- Recall procedures (What FDA expects from you.)

- FDA Field Office Management

- FDA Center(s) Management

- The firm's job

- FDA enforcement actions

- Follow up inspections

- Foreign Inspections

Who Should Attend:

- Regulatory Affairs Directors

- Quality Assurance Managers

- Quality Control Managers

- Manufacturing Directors and Managers

- Product Risk Managers

- Venture Capitalists

For more information about this conference visit http://www.researchandmarkets.com/research/tz5jnz/managing_your_fda

Contacts

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Related Topics: Pharmaceutical Manufacturing

Contacts

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Related Topics: Pharmaceutical Manufacturing