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Data Privacy: Global Regulations and Expectations

Please check back later for this seminar's current schedule, or review our other live seminars for similar courses.

Course Description

Researchers who conduct clinical research have questioned how the Privacy Rule affects their research activities. The impact of non-compliance has increased and intensified a great deal. In this web seminar you will learn about the expanded definitions of covered entity, business associate, unauthorized disclosures, penalties, and more. We will also discuss data privacy challenges, and how to share relevant data while protecting personally identifiable information from misuse on a global level in clinical trials.

Learning Objectives

  • Present HIPAA concepts and terminology specific to conducting clinical trials
  • Review the history of HIPAA and the impact on clinical research
  • Describe covered entities’ roles and responsibilities
  • Discuss the types of data that require protection
  • Review the legislation that applies
  • Examine the differences in data privacy expectations in global clinical trials and consider how this impacts the industry 

Who Should Attend

  • Project Managers
  • Site Managers
  • Clinical Research Coordinators
  • Research Nurses
  • Investigators
  • Quality Assurance Personnel
  • Regulatory Affairs Professionals
  • Clinical Research Associates
  • Clinical Research Associate Managers

Instructor

Sandy Soliman

Click here for complete trainer biographies 

Registration Fees

$695

Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.

Accreditation Information
 

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 2 hours (0.2 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation.  Barnett International will mail ACPE statements within three weeks of program completion.  ACPE#: 0778-0000-12-078-L01-P.  Released: 8/12. 

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471 

 

 

 

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On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
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GCP for Investigators
 

Barnett’s scenario-based eLearning course is designed with the busy Principal Investigator in mind.  Based on real-life scenarios encountered by investigative site teams, this highly focused 7-module GCP training is designed to ensure comprehensive understanding of the key components of GCP.

For more details on this scenario-based eGCP program for investigators please click here. 


BARNETT CATALOG The Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year. 

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Blended Curriculum Path for the CRA, CRC, and Project Manager

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Live SeminarLIVE SEMINARS

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Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


Web SeminarWEB SEMINARS

10-Week CRA & CRC Beginner Program  

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance 

Use of Notes to File in Clinical Trial Essential Documentation 

10-Week Clinical Research Associate (CRA) On-Boarding Program  


PublicationsPUBLICATIONS

2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)