How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings | September 24, 2015 8:30 AM - September 25, 2015 3:30 PM | Automation.com

How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings

Event Summary

DATE:
September 24, 2015 - September 25, 2015
LOCATION:
San Francisco, CA 94108
COUNTRY:
USA
START DATE/TIME:
September 24, 2015 8:30 AM
END DATE/TIME:
September 25, 2015 3:30 PM
EVENT TYPE:
Training
HOST:
ComplianceOnline
PHONE:
888-717-2436
EMAIL:
[email protected]
WEBSITE:
Click here to Visit

Description

Course Description:
Despite a few guidance documents to help sponsors prepare for meetings with the FDA, it is a challenge to understand the most efficient and productive ways to strategize, prepare, conduct, and follow-up for these meetings. There are many misconceptions about the expectations from these meetings both for the sponsor and the FDA, and hence many sponsors fail to get the most benefit from them. Over the years, the FDA has also revised processes and practices for meeting with sponsors.

This two day seminar will provide valuable tips about the logistics, planning, conduct and best practices for all kinds of meetings with the FDA. Throughout the workshop, the author will discuss case studies and examples to highlight the common errors and potential solutions. This workshop contains a collection of practical tips from the instructor’s extensive FDA meeting experience. This one-of-a-kind workshop will provide step-by-step instructions and practical tips to the most productive meeting with FDA for all FDA-regulated organizations.



Learning Objective:
Understanding different stages of FDA meetings: pre-IND, Pre-IDE, Pre-NDA, pre-PMA, End-of-Phase 2
Creating rationale for FDA meetings
Requesting process for FDA meetings
Creating a meeting information package and its regulatory requirements
Logistics of an FDA Meeting
Learn FDA meeting follow ups


Who will Benefit:
Regulatory affairs professionals
Senior management executives (CEO, COO, CFO, etc.)
Project managers
Clinical trial specialists
Regulatory compliance associates and managers
People investing in FDA-regulated product development projects


For Registration - http://www.complianceonline.com/how-to-prepare-for-an-fda-meeting-of-pre-ind-ide-pre-nda-seminar-training-80111SEM-prdsm?channel=automation


Note: Use coupon code 232082 and get 10% off on registration.

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