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 Conferences & Online Training




Conference Registration

 


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

 

On-Site Conferences

 

8th Trial Master File Summit - Jan. 22-24 - Orlando, FL

2nd Innovative Regulatory Pathways Summit - Jan. 28-29 - Arlington, VA

Risk Evaluation and Mitigation Strategies Summit - Jan. 28-29 - Arlington, VA

Human Factors Usability Studies Summit - Feb. 4-5 - San Francisco, CA

Medicare Conference 2019 - Feb. 25-26 - Austin, TX

Real-Time Benefit Verification and Electronic Prior Authorization Forum - Feb. 25-26 - Austin, TX

13th Annual Clinical Trial Billing & Research Compliance Conference - Mar. 3-6 - Orlando, FL

 

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

Technical Writing in an Industrial Environment
Jan. 9, 2019

Human Factors Usability Studies Following ISO 62366 and FDA Guidance
Jan. 9, 2019

The Federal False Claims Act : Latest Updates and Risk Mitigation Strategies
Jan. 10, 2019

Methods For Detecting Mycoplasma Contamination In The Manufacture Of Pharmaceuticals And Biologics
Jan. 10, 2019

Essentials of Post Market Surveillance and Vigilance - Do you know the requirements?
Jan. 10, 2019

Fungal Contamination and Pharmaceutical Products Recall
Jan. 10, 2019

Tobacco Industry Trends For Computer Systems Regulated By FDA
Jan. 14, 2019

NCMR Simplified - A One-Form, Easy-to-Complete, Method for Simplifying your NCMR Process
Jan. 16, 2019

Writing Effective 483 and Warning Letter Responses
Jan. 16, 2019

Issues in Calibrations and Accuracy in Method Validation
Jan. 16, 2019

How to Demonstrate Vendor-CRO-CMO Oversight in the Biopharma and Device Industry
Jan. 22, 2019

IEC 62304 for Medical Device Software
Jan. 23, 2019

How to Prepare for FDA Inspections and Customer Audits of Pharmaceuticals
Jan. 24, 2019

FDA Precedent: Procedural Steps to Issue a Mandatory Recall of Herbal Drug
Jan. 24, 2019

Efficient and Effective Batch Record Reviews to Improve your Process Capabilities
Jan. 29, 2019

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory
Jan. 29, 2019

GMP's for Medical Marijuana - Insight into Manufacturing, Labeling, Tracking and Disposal requirements
Jan. 29, 2019