FDA Newswatch

 Conferences & Online Training




Conference Registration

 


To Register Online click on a link below
or
Call: 201-871-0474  Fax: 253-663-7224

 

Online Training


* 60-90 minute seminar (Travel-Free) delivered over the phone and internet.
* Unlimited listeners per connection - bring the entire department.
* Continuing education credits available for most teleconferences

Post Market Surveillance for Medical Devices
Jun. 8, 2017

Regulatory Guide for Medicare Claim Management of ADRs (Additional Development Requests)
Jun. 8, 2017

How to Analyze PQ Data with Multiple Populations/ Failure Modes using Minitab®
Jun. 9, 2017

Managing GLP Studies in Non-GLP Facilities
Jun. 9, 2017

21 CFR Part 11 and Annex 11 Compliance - Specifics Needed to Eliminate 483s
Jun. 13, 2017

Pharmacokinetics/Biopharmaceutics for Chemists/Analysts
Jun. 13, 2017

Supplier and Service Provider Controls: FDA Expectations
Jun. 14, 2017

How to Establish and Maintain a Design History File for a Medical Device
Jun. 14, 2017

Grievances and Complaints: What Hospitals Should Know about the CMS, Joint Commission, DNV and OCR Standards?
Jun. 14, 2017

Vendor Qualification for Quality Services
Jun. 14, 2017

Medical Device - Engineering change control
Jun. 21, 2017

Secrets for Writing Excellent SOPs (Standard Operating Procedures)
Jun. 22, 2017

Nursing: CMS CoP Standards for Hospitals and Proposed Changes: 2017 Update
Jun. 22, 2017

How FDA & FTC Regulate Advertising & Promotion of OTC Drugs & Dietary Supplements
Jun. 27, 2017

Ensuring Compliance with FDA and EMA Global Labeling Requirements
Jun. 27, 2017

Writing Effective Standard Operating Procedures and Work Instructions
Jun. 28, 2017

Prescription and Over-the-Counter GMPs: Avoiding FDA Form 483 and Making the Best Decisions
Jun. 28, 2017

Equipment Validation, Tracking, Calibration and Preventive Maintenance
Jun. 30, 2017