The No. 1 Trade Show Site in the U.S.

Menu
×
EVENT DATE
Sep 2016
M T W T F S S
19202122232425
EXPO DATE
Sep 2016
M T W T F S S
19202122232425

Venue


Online Event
Location map
Tel:
Type: Online Event

HOTEL DEALS

Booking.com

TRAVEL DEALS

Expedia.com

Partners

exhibitus success by design Remington Hotels

Falsifying Data in clinical trials. What to report - By Compliance Global Inc.

B2B

EVENT DESCRIPTION

Overview:

Unfortunately, each year there are headlines stating that some researcher has falsified, fabricated or plagiarized all or part of the research data. Should this activity have been reported, by who and when?

Why Should You Attend:

Looking at several case examples we can learn what to look for and what to report. We will also discuss the regulations governing the ethical conduct of human subjects research.

Areas Covered in this Webinar:

Research integrity charges in and of themselves can be devastating to the researcher and the institution. Not all activity that is questionable involves a violation of research integrity so knowing who to ask or where to go for guidance can help avoid a compromising situation.

Conversely, know the rules before and while the research is conducted creates a culture of compliance which helps avert problems.

Learning Objectives:

•  What is research integrity?

•  Definitions for falsification, fabrication and plagiarism

•  What types of problems are created?

•  What should be reported?

•  Where should those reports go?

•  Who monitors and governs research integrity?

Who Will Benefit:

•  Human Subjects Research Personnel

•  Clinical Research Coordinator Positions

•  Investigator Positions

•  Administration in charge of Clinical Research

•  Regulatory Compliance Personnel

Speaker Profile:

Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program.  

She has initiated the planning, development, authorship and implementation of many human subjects’ research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities. She has provided consultation regarding ethical, federal, state, and institutional requirements for faculty and staff both in the design and execution of their projects and teaches research ethics and regulatory affairs and the fundamentals of research management to graduate and undergraduate students.

For more detail please click on this below link:

http://bit.ly/2aVMU0b

Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515

Fax: +1-516-900-5510

There may be many networking opportunities at the Falsifying Data in clinical trials. What to report - By Compliance Global Inc.. Find out more in the event details below.

EVENT CONTACTS

Sign Up for FULL Membership and Log In to access Event Contact Information.

EVENT DETAILS

Primary Industry:
Clinical Pharmacology
Other Industries:
Clinical Pharmacology, Professional Healthcare
Audience:
Human Subjects Research Personnel

Clinical Research Coordinator Positions

Investigator Positions

Administration in charge of Clinical Research

Regulatory Compliance Personnel
Notes:
Show Owner:
Compliance Global Inc.
Sponsorship: Yes

Exhibitor Information +

Booth Details:

Booth Size
Booth Cost
No Exhibiting
Amenities
Electricity:
n/a
Water:
n/a
Generator:
n/a
Marketing Vehicles Allowed:
n/a
Services
n/a
Show Owner
Compliance Global Inc.

floor plan

MORE events +

BUSINESS+
HEALTH CARE+
MANUFACTURING+
TECHNOLOGY+

Display Makers

Promo Makers

2017: 2,575 Trade Shows
2018: 575 Trade Shows
© copyright since 2008 All Rights Reserved eventsinamerica.com
704
page views