SafetyCall’s Industry Expert, Dr. Rick Kingston Speaks at Upcoming Events

Safetycall’s Dr. Rick Kingston will be presenting on serious adverse event reporting (SAER) data and observations during an upcoming AHPA webinar.

Joining Dr. Kingston will be Ashish Talati, a partner with Amin Talati & Wasserman, and one of the industries foremost experts on FDA regulatory matters. In addition AHPA Chief Information Officer Dr. Merele Zimmermann will participate. The topics covered …

Listen in as SafetyCall’s Rick Kingston Speaks at FDA Public Hearing

The FDA is seeking public comment regarding the availability of scientific data and information regarding Cannabis or Cannabis derived ingredients.  This has been a difficult topic for FDA considering the fact that such products are still classified as Schedule I substances at a Federal level. FDA is looking for scientific information to help them determine if there is a path

CRN Presents Free Webinar on Supplement Safety

Dr. Rick Kington will be the featured presenter during a free webinar for pharmacists and nurse practitioners (NPs) on dietary supplements and adverse event reporting results.  The webinar is sponsored by The Council for Responsible Nutrition (CRN) and will take place on Thursday, March 3, at 1:00pm Eastern.  The webinar is presented exclusively to members of Skipta’s Pharmacist Society and …

Webinar: The Buzz on Caffeine

Dr. Kingston will join a group of faculty to present a two hour webinar hosted by the Institute of Food Technologists.

“The Buzz on Caffeine: New Developments in Safety, Regulation and Adverse Event Reporting

Caffeine, a methylated xanthine, is the most widely used mild central nervous system stimulant, naturally present in many common conventional foods and dietary supplements.  More …

Webinar: Best Practices for Adverse Event Management and Reporting

On August 9, 2012, Rick Kingston, President, Regulatory and Scientific Affairs at SafetyCall International, will be presenting as a part of the SOCAP International Webinar Series. His presentation is titled, “Best Practices for Adverse Event Management and Reporting” and will cover:

  • Potential implications of pending and newly-implemented changes to regulations over adverse event reporting requirements for consumer products.
  • FDA’s new

Is your Company Compliant? Learn More at our “Best Practices” Webinar

“Best Practices” for post-market surveillance & regulatory reporting of dietary supplement and OTC drug adverse events.

Although “Best Practice” AE Processes can be fairly straightforward, there are a variety of challenges a manufacturer must overcome when implementing an AE system. These can include designing a database, developing SOP’s for managing, documenting, analyzing and reporting indicated events, and overcoming internal …

Webinar: How the CCPSA WILL Affect Your Business

This webinar provided by SafetyCall International will explore the wide reaching impact of the recently initiated Canadian Consumer Product Safety Act (CCPSA) as it relates to manufacturer responsibility and consumer care. The goal is to help manufacturers adjust to the ever-changing regulatory environment and to prepare themselves internally for new reporting timelines and more stringent compliance measures.

Presented by …

Webinar: CCPSA to be Offered by SafetyCall

A webinar designed to help manufacturers understand and prepare for the ramifications of the new Canada Consumer Product Safety Act (CCPSA) will be presented at 12:00 p.m. CDT on September 14, 2011, by SafetyCall International, an industry leader in adverse event management and post-market surveillance services for industry.

The webinar, “How the Canadian Consumer Product Safety Act WILL Affect Your …