Controlled Substances in Clinical Research Settings

Provides learners with key information on the management of controlled substances in clinical research settings.

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About this Course

Individuals and organizations planning to handle, use, or study controlled substances in their research or other professional practices must understand the risks and regulatory responsibilities associated with employing these substances. They must comply with federal, state, and local requirements and establish best practices to prevent and mitigate those risks.

This in-depth course provides learners with an overview of the U.S. federal and select state laws and regulations that govern the use of controlled substances in clinical research, including the requirements for their acquisition, usage, storage, final disposition, and recordkeeping. It provides guidance for registrants/licensees and organizations on how to establish and maintain compliance with the controlled substances regulations. The course also reviews the mechanisms of action and abuse potential of controlled substances by pharmacological class. It further discusses considerations for the development of an effective program to prevent and mitigate diversion of controlled substances as well as guidance regarding how to prepare and respond to internal and external audits and inspections.

Course Preview:

Language Availability: English

Suggested Audiences: Clinical Investigators, Faculty, Researchers, Staff, Students

Organizational Subscription Price: $675 per year/per site for government and non-profit organizations; $750 per year/per site for for-profit organizations
Independent Learner Price: $99 per person

Demo Instructions


Course Content

Introduction to Controlled Substances

This module explores the oversight of controlled substances, which are tightly regulated due to their abuse and dependence potential. In the U.S., federal laws and regulations set forth how federal oversight and enforcement mechanisms control the life cycle of these substances. Each state also establishes its own rules and regulations on various uses and users of controlled substances. This module introduces the regulatory framework for the use of controlled substances in the U.S. More specifically, it reviews U.S. laws and regulations; the controlled substance schedules; the federal and state authorities responsible for enforcement; federal and state authorizations associated with the manufacturing, distribution, storage, dispensing, and use of controlled substances; and schedule-based requirements.

Recommended Use: Required
ID (Language): 20716 (English)
Author(s): Ji-Eun Kim, PhD, RPh, RAC - Northwell Health

Understanding Controlled Substances

There is inherent risk to the use of controlled substances and chemicals in research. To limit the risks, it is imperative that researchers are aware of the abuse and diversion potential of the products they will use in their studies. All aspects of the research apparatus are responsible for mitigating these risks, including individual researchers and staff, internal and external oversight bodies, and institutional leadership. This module provides an overview of the differences between controlled substances, precursor chemicals, and controlled chemicals as well as the pharmacological properties and medical uses of controlled substances. Learners will also review how controlled substances are abused and relate this to theft, loss, and diversion. The module concludes with a review of institutional governance (such as review committees or oversight bodies) that monitor and evaluate the use of controlled substances and how to mitigate and prevent a theft, loss, or diversion. 

Recommended Use: Required
ID (Language): 20717 (English)
Author(s): Melissa A. Scotti, PhD, CIP - Northwell Health

Management of Controlled Substances – Part 1 (Security, Controls, and Processes)

Controlled substances can be highly dangerous and addictive. For this reason, it is important to have controls in place to prevent theft and the diversion of controlled substances. The U.S. Drug Enforcement Agency (DEA) regulations provide specific security requirements for the storage of controlled substances. The DEA also evaluates the security of systems to determine compliance with its regulatory requirements. There may be additional requirements through state law, local institutional/facility policy, and research sponsors. This module focuses on the requirements for storage, procurement, delegation, and final disposition. The Management of Controlled Substances – Part 2 (Documentation and Maintaining Compliance) module explores the documentation requirements for maintaining compliance and reporting requirements for loss, theft, or diversion of controlled substances.

Recommended Use: Required
ID (Language): 20718 (English)
Author(s): Melissa Naraine, MA, CCRC - Northwell Health; Stephen Frattini, DVM - Northwell Health

Management of Controlled Substances – Part 2 (Documentation and Maintaining Compliance)

As part of a robust plan to manage controlled substances, facilities should develop appropriate procedures for documentation and recordkeeping to effectively track the life cycle of controlled substances. This includes retaining and maintaining all required documents associated with controlled substance transactions and establishing a monitoring system to evaluate and reconcile inventory. This module explores the regulatory requirements for documentation and covers the reporting requirements for the loss, theft, or diversion of controlled substances.

Recommended Use: Required
ID (Language): 20719 (English)
Author(s): Melissa Naraine, MA, CCRC - Northwell Health

Preparing for an Audit or Inspection

Federal and state regulations are heavily focused on preventing inappropriate access to and diversion of controlled substances. Audits and inspections of an organization’s controlled substance program are important not only to verify compliance with the regulations, but to ensure public safety and security. Diversion of controlled substances from appropriate clinical research use can result in detrimental and even deadly consequences. This module discusses how a well planned and executed program, including internal and external audits and inspections, can decrease the organization’s risk of diversion.

Recommended Use: Required
ID (Language): 20720 (English)
Author(s): Stephen Frattini, DVM - Northwell Health; Hamangi Patel, LMSW, CHRC, RQAP-GCP, CCRP - Northwell Health


FAQs

Who should take the Controlled Substances in Clinical Research Settings course?

The suggested audience includes individuals who work with or are responsible for the management of controlled substances in clinical research settings (such as researchers, clinical investigators, students, staff, and faculty).

How long does it take to complete the Controlled Substances in Clinical Research Settings course?

This course consists of five required modules. The modules contain detailed content and graphics, and each module includes a quiz.

Modules vary in length, and learners may require different amounts of time to complete them based on their familiarity and knowledge of the topic. However, the entire course should take about two hours to complete.

What are the standard recommendations for learner groups?

This course is designed such that learners should complete all five required modules in sequence.

Is this course eligible for continuing medical education credits?

This course does not currently have CE/CME credits available.

Why should an organization subscribe to this course?

Organizational subscriptions provide access to the organization's affiliated members. This allows organizations to train individuals across the organization on the management of controlled substances.


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