What’s New

 

Joshua Sharlin, Ph.D.

Sharlin Learning & Consulting

Three December 2012 Audioconferences

To Register call FOI Services, Inc at 301-975-9400

Presentation Title (3 classes)

Description

Date & Time

Applies to

Audience

To Register

(Click on the registration button for the desired audioconference.)

1

Annual Reports: SOPs for Developing Content Which Meets FDA Requirements A discussion about the SOPs needed by drug, biologic and device firms in order to prepare annual reports which comply with FDA requirements. Tues, Dec 4,
1 to 2:30 pm EDT
Drugs, Medical Devices and Biologics Everyone with a role in creating or reviewing annual reports

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2

What Needs to be in a Product Submission: An FDA Reviewer’s Perspective (TC# 1666) A discussion about how FDA reviewers think and work –  and how to apply this knowledge to improve the  structure and content of your FDA submissions Mon, Dec 10, 1 to 2:30 pm EDT Drugs, Medical Devices and Biologics Everyone interested in creating reviewer friendly submissions

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3

Adverse Event ReportingSOPs for Drugs & Biologics

 

A discussion about Standard Operating Procedures (SOPs) to help you organize and improve your FDA compliance with drug and biologic safety reporting efforts. Wed, Dec 12, 1 to 2:30 pm EDT Drugs and Biologics Everyone with a hands-on or management role in safety reporting

Register Now