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Overview of the Clinical Research Process

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A UL EduNeering course

A pharmaceutical, biological, or medical product is generally not introduced into the marketplace unless it has been approved by a country’s regulatory agency. This basic course is designed to give an understanding of the approval process and the importance of developing products that meet regulatory requirements for global registrations. The safety and efficacy of products are approved via clinical trials in humans, by investigators who have demonstrated that the research was conducted under the auspices of good clinical practices (GCPs). The principles and applications of GCPs are essential in product development, and they are based on regulations, directives, and guidelines meeting global regulatory demands in the conduct of clinical research. All personnel involved in new product development—from bench scientists who discover the compounds or devices to researchers to marketing and sales personnel—should be aware of what is necessary to bring a new pharmaceutical or medical product to market.

Featured Topics 

  • Regulations, directives, and guidelines that govern product development
  • Phases of clinical research that follow GCPs
  • Timelines and costs

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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