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Avera Research Integrity Conference

Avera Research Integrity Conference

September 10, 2021 • 7:30 am - 7:00 pm

A regional conference on Responsible Conduct of Research (RCR) will be held at 7:30 a.m. – 7 p.m. CDT on Friday, Sept. 10, at the Hilton Garden Inn Downtown.

The Avera Office of Research Compliance has received a grant from the federal Office of Research Integrity to host this conference. The University of South Dakota is one of the co-sponsors, along with several other South Dakota universities and organizations.

CNE, CME, Pharmacy and ACRP CEUs through ACRP MN Chapter will be provided for in-person attendees.

Livestreaming will be offered to registered attendees unable to attend in-person.

It is each researcher’s responsibility to ensure that all research done under his/her direction is carried out in an ethical and legal manner. To assist with this, the National Science Foundation (NSF) and National Institutes of Health (NIH) have selected certain foundational topics in Responsible Conduct of Research, aimed at developing graduate students and postdocs, in particular. It is recommended that all researchers attend such training every 4 years throughout their careers.

Description

The overall goal of the conference is to provide education to create a culture of research integrity to prevent research misconduct. Attendees and presenters will discuss how individuals and organizations can support researchers in establishing proper protocols to support transparency that results in an increased understanding of research compliance and decreased risk for research misconduct.

Target Audience

  • Specialties — Nursing, Pharmacist, Physician, Research
  • Professions — Nurse, Nurse Practitioner, Pharmacist, PhD, Physician, Physician Assistant, Student

Registration Information

  • Registration Fee: This event is offered at no charge to participants
  • In Person: CE credit is being applied for all day
  • Virtual: No credit is offered for the morning session (table discussions with faculty won’t be available virtually)
  • Virtual: CE Credit is being applied for afternoon session

ACCME Objectives

  • By the end of this learning activity participants will be able to differentiate errors from deliberate non.
  • Participants will be able to evaluate Investigator and Research Coordinator competencies.
  • Identify specific and unique ethical, regulatory and cultural aspects of conducting research with Native American Communities.
  • Recognize common elements to research misconduct cases in both administrative and legal contexts.
  • Learn about hypothetical (but realistic) scenarios in which a researcher must make a difficult decision that will help participants understand that not all situations are black and white.
  • Select the right investigation methods and tools to identify root cause.
  • Learn about the consent process and make the informed consent document more understandable.
  • Be able to identify the benefits of mentoring and stages of the mentoring process.
  • Understand challenges in data integrity in medical device design and development. Learn about regulations for Data Integrity requirements by the FDA for medical devices.
  • Learn about some of the advantages and disadvantages of decentralized clinical trials. Learn about what some of the points to consider when embarking on a decentralized clinical trial.

ANCC Learning Outcomes

  • By the end of this learning activity participants will be able to differentiate errors from deliberate noncompliance, falsification and fraud.
  • Participants will be able to evaluate Investigator and Research Coordinator competencies
  • Identify specific and unique ethical, regulatory and cultural aspects of conducting research with Native American Communities
  • Recognize common elements to research misconduct cases in both administrative and legal contexts
  • Learn about hypothetical (but realistic) scenarios in which a researcher must make a difficult decision that will help participants understand that not all situations are black and white.
  • Select the right investigation methods and tools to identify root cause.
  • Learn about the consent process and make the informed consent document more understandable.
  • Be able to identify the benefits of mentoring and stages of the mentoring process.
  • Understand challenges in data integrity in medical device design and development. Learn about regulations for Data Integrity requirements by the FDA for medical devices.
  • Learn about some of the advantages and disadvantages of decentralized clinical trials. Learn about what some of the points to consider when embarking on a decentralized clinical trial.

Additional Information

ADA accommodations will be made in accordance with the law. If you require ADA accommodations, please indicate what your needs are at the time of registration. We cannot ensure the availability of appropriate accommodations without prior notification.

By registering, you agree to prevent any unauthorized copying, recording, use, distribution and/or re-broadcast of this course. You are not authorized to record lectures or content.

Organizers

Avera Health

Website: View Organizer Website

University of South Dakota

Phone: 877-269-6837Website: View Organizer Website

Venue

Hilton Garden Inn Downtown
201 E 8th Street
Sioux Falls, SD 57103 United States
+ Google Map
View Venue Website