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Introduction to Medical Device Health Care Compliance

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A UL EduNeering course

This course provides high-level introduction and background regarding the compliance environment affecting the medical device industry. The course is designed to make employees aware of pertinent laws, regulations, and industry guidance that pertain to this industry. These topics are especially important because medical device product development involves close collaboration between the industry and health care professionals and the use of such devices may require the interaction and skill of medically trained personnel.

Featured Topics 

  • US Food and Drug Administration (FDA) regulations
  • State ethics and compliance legislation
  • Foreign Corrupt Practices Act
  • Federal anti-kickback laws
  • Office of the Inspector General Compliance Program Guidance
  • AdvaMed code of ethics

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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