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Drug Safety & Adverse Event Reporting

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Overview 

A UL EduNeering course

This course reviews the history and evolution of drug safety. An exploration of US pharmacovigilance, this course introduces learners to the regulatory requirements in the clinical trial and post-marketing environments and to international drug safety monitoring efforts.

Featured Topics 

  • History and evolution of drug safety in the United States
  • Developments in drug safety monitoring and adverse event reporting
  • Drug safety monitoring efforts in the nonclinical trial environment
  • Clinical reports
  • Postmarketing
  • Postmarketing reports
  • International safety

Who Should Attend 

Professionals and experts in the pharmaceutical, biotechnology, and medical device fields

Special Offers 

Save by purchasing multiple UL EduNeering eLearning modules at one time. One to two modules cost $99 each, three to four cost $89 each, five to nine cost $80 each, and 10 or more cost $65 each.

Contact Information 

Linda Belmont, DIA
Phone +1.215.293.5818
Linda.Belmont@diahome.org

Technical Requirements 

Click here for minimum system requirements.

Registration Fees 

Other Fees

Individual
$99.00
Group Discounts

When purchasing multiple UL EduNeering eLearning modules in one transaction, the following discount prices apply:

·          1 to 2 modules are $99.00 each

·          3 to 4 modules are $89.00 each

·          5 to 9 modules are $80.00 each

·          10 or more modules are $65.00 each

Register Online

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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