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Aspects of Regulatory History

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Overview 

A UL EduNeering course

This course will provide an overview and summary of the regulatory history of the US Food and Drug Administration (FDA) and International Conference on Harmonisation (ICH), and the requirements for ensuring proper and successful clinical trial execution. This module includes some of the history behind today’s system of drug and device development. Participants who take this course will be able to recognize the evolution of the industry and the FDA. Learners will understand the ICH and its global impact on the medical product industry.

Featured Topics 

  • Standards for pharmaceutical and medical device development
  • US and international regulatory organizations
  • Regulations and guidelines

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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