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ForwardGood Research Practices 10.23.19
Overseeing a research study can be challenging, especially if you are new to the research environment. This workshop will provide an overview of the various components of Good Research Practices. Topics to be discussed include: Federal Regulations Governing Human Subject Research, Tips for Protocol Adherence, Investigator Responsibilities, Informed Consent, Study Documentation, and Regulatory File Maintenance. This program is strongly encouraged for new investigators and coordinators as they start their clinical research careers as well as those with research experience.
Target Audience
THIS ACTIVITY IS INTENDED FOR PROVIDERS IN THE SPECIALTIES OF:
Addiction Medicine
Cardiology
Critical Care (Intensivists)
Dermatology
Endocrinology
Gastroenterology
Geriatric Medicine
Gynecological/Oncology
Hematology/Oncology
Infectious Disease
Neurology
Pediatric Medicine
Peripheral Vascular Disease
Physical Medicine and Rehabilitation
Preventive Medicine
Psychiatry
Pulmonary Disease
Rheumatology
Sleep Medicine
Sports Medicine
Unknown Physician Specialty
Learning Objectives
Learning objective is to provide an overview of Good Clinical Practice as they relate to:
The Federal Regulations & NIH Policy
Protocol Adherence
PI Responsibilities
Informed Consent
Study Documentation
Agenda
*Introduction and Review of RCCO and Federal Regulations
*Review of Tips for Protocol Adherence
*Review of PI Responsibilities
*Informed Consent Process
*Study Documentation
*Questions
Disclaimer Statement
The information presented at this CME program represents the views and opinions of the individual presenters, and does not constitute the opinion or endorsement of, or promotion by, the UPMC Center for Continuing Education in the Health Sciences, UPMC / University of Pittsburgh Medical Center or Affiliates and University of Pittsburgh School of Medicine. Reasonable efforts have been taken intending for educational subject matter to be presented in a balanced, unbiased fashion and in compliance with regulatory requirements. However, each program attendee must always use his/her own personal and professional judgment when considering further application of this information, particularly as it may relate to patient diagnostic or treatment decisions including, without limitation, FDA-approved uses and any off-label uses
Kelly Dornin-Koss, MPPM, RN, CIP
Research Conduct and Compliance Office
University of Pittsburgh
Telephone: 412/383-1711
Email: kld1@pitt.edu
Disclosures: No members of the planning committee, speakers, presenters, authors, content reviewers and/or anyone else in a position to control the content of this education activity have relevant financial relationships with any proprietary entity producing, marketing, re-selling, or distributing health care goods or services, used on, or consumed by, patients to disclose.
In support of improving patient care, the University of Pittsburgh is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Physician (CME)
The University of Pittsburgh School designates this live activity for a maximum of 2.0 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Other health care professionals will receive a certificate of attendance confirming the number of contact hours commensurate with the extent of participation in this activity.
Available Credit
- 2.00 AMA PRA Category 1 Credit™The University of Pittsburgh School of Medicine is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
- 2.00 Attendance