Upcoming ORC Trainings

Essentials of Quality Research Regulations
Date: Wednesday, February 28, 2018
Time: 8:00 AM-4:00 PM
Location: ED II G131A

  • Training on the Basics of Research
  • Fundamentals of Conducting Research
  • Available Research Support
  • Informed Consent
  • GCP Documentation Practices

(CRS Requirement)

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Developing a Research Protocol
Date: Wednesday, March 7, 2018
Time: 11:00 AM – 12:30 PM
Location: ED II G141B

  • Overview of Research  Protocol Development
  • CLARA Overview

(CRS Requirement)

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Writing Standard Operating Procedures
Date: March 15, 2018 (Tentative)
Time: TBA
Location: TBA

  • Overview of FDA/IRB Protocol in

(CRS Elective)

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Research Misconduct 
Date:  Thursday, March 29, 2018
Time: 12:30 PM-2:30 PM
Location: ED II 8/121

  • Importance of Research Misconduct
  • Findings of Research Misconduct
  • Responsibilities of Federal Agencies and Research Institutions

(CRS Elective)

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Protocol Deviations
Date: Wednesday,  April 18, 2018
Time: 11:00 AM – 12:00 PM
Location:  ED II G131 A

  • Adhere to Protocol Findings by the FDA and ORC
  • Tracking and Reporting Deviations
  • Discuss Importance of Research Misconduct

(CRS Requirement)

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Reportable New Information & the IRB

Date: Thursday,  April 26, 2018
Time: 11:00 AM – 12:00 PM
Location: RAHN 3/202

  • Examine Methods of Reporting Research Study Activities to the IRB
  • Helpful Tools for Submitting Documentation

(CRS Requirement)

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Advanced Research Ethics

Date: Thursday, May 3, 2018
Time: 12:30 PM – 4:30 PM
Location: ED II B107

  • Examines the Ethical Questions  in Regards to Human Subjects in Research

(CRS Requirement)

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Research Billing

Date: Wednesday, May 9, 2018
Time: 11:00 AM – 12:00 PM
Location: IDW 115A

  • Evaluation of Proper Billing Practices in Medical Research

(CRS Requirement)

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