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Clinical Trial Audits and Consequences of Non-Compliance

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A UL EduNeering course

Sponsors of clinical trials can institute measures to keep researchers in compliance with trial rules and regulations. However, those controls are only effective if personnel apply them properly. This course describes the clinical trial audit process and how audits are used to ensure that trials are conducted in accordance with regulatory requirements. The typical actions that investigators can take for noncompliance will also be covered.

Featured Topics 

  • Clinical trial audits
  • Compliance with clinical trial regulations and noncompliance consequences
  • Clinical trial audit process
  • US Food and Drug Administration clinical trial inspections

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 +

Technical Requirements 

Click here for minimum system requirements.

Registration Fees 

Other Fees

Group Discounts\Registration

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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