SEARCH

UPCOMING LIVE SEMINARS
 






Transitioning Pharmaceutical Professionals to Medical Device April 2010

Apr 5, 2010
Order the DVD of this seminar

Course Description

This course assists study managers, program managers, CRAs, and other pharma professionals in learning more about the differences between pharma and medical device studies, including objectives, protocol creation, and quality systems regulations. The course will help professionals learn about the most popular medical device therapeutic areas, the engineering component/ R&D/preclinical, as well as the technical procedures of those therapeutic areas.

VideoPreview

Learning Objectives

  • Identify the differences between pharmaceutical and medical device studies
  • Identify the key regulations of medical devices
  • Explain the QSR process

Who Should Attend

  • Professionals wanting to learn more about the medical device industry
  • Pharmaceutical professionals who are new to medical device industry
  • Other professionals who are new to medical device industry
  • CRAs
  • Regulatory professionals
  • Management professionals
  • Clinical sites who will be conducting medical device trials

Instructor

Douglas Albrecht, B.S.N., C.C.R.A. 

Click here for complete trainer biographies

Course Length Time

2 hours; 1:00 – 3:00 p.m. Eastern

Course Dates

April 5, 2010

Hold this course at your company!

For more information, contact Naila Ganatra at (215) 413-2471

FOLLOW US ON: 

LinkedIn twitter Facebook 


On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
For details on our scenario-based practical GCP application on-demand course, click here.


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. 

Jan - July 2014 Edition

Winter CatalogDownload Today!  

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

BCP Cover

Download Today! 

 

 

 


 

DVD IconWEB SEMINAR ARCHIVE 

 View Catalog of Offerings   

New Titles added every month! 
Course Alumni Save 50% 


Live SeminarLIVE SEMINARS

Monitoring Clinical Drug Studies: Intermediate 

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)