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<<<June 2013>>>
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Jun, 2013

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Building Relationships with Clinical Research Sites delete
29
Changes and Challenges in Foreign Clinical Research delete
RECIST 1.0 & 1.1: Overview/Data Challenges in Oncology Clinical Trials delete
30
Quality Risk Management in Clinical Trials and Pharmacovigilance delete
31
Regulatory Intelligence delete
01 Jun
2
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Writing and Updating the Investigator's Brochure delete
4
Monitoring Plan Development delete
5
Adequate Sponsor Monitoring Systems delete
6
FDA's BIMO Program: Inspection of Sponsors, CROs, and Monitors delete
Electronic Source Documentation: Navigating the FDA Draft Guidance delete
7
Good Clinical Practice: Practical Application and Implementation delete
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Informed Consent Content & Process Requirements delete
11
Real-World Monitoring: Tips for Success and Sanity delete
12
Collaborating with CROs delete
13
Principal Investigator Oversight & the Appropriate Delegation of Tasks delete
14
10-Week Clinical Research Associate (CRA) On-Boarding Program delete
Implications of New FDA Guideline Risk Based Approach to Monitoring delete
more...
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Strategies for Remote Monitoring delete
19
The GCPs of Essential Documents delete
20
Drug Development and FDA Regulations delete
GCP Training for Investigators delete
21
Tools for Trainers: Clinical Research Job-Aids and Checklists delete
22
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24
Use of Notes to File in Clinical Trial Essential Documentation delete
Principal Investigator Training: Roles and Responsibilities delete
25
Trial Master Files: Why They Are Important & How to Organize Workshop delete
26
Medical Device Development: U.S. and EU Differences delete
Data Privacy: Global Regulations and Expectations delete
27
How to Write Effective Monitoring Reports and Communications Workshop delete
28
Adverse Event Monitoring for CRAs delete
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01 Jul
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Upcoming Web Symposia

6/20/2013
GCP Training for Investigators(3)


6/20/2013
Drug Development and FDA Regulations(7)


6/21/2013
Tools for Trainers: Clinical Research Job-Aids and Checklists(2)


6/24/2013
Use of Notes to File in Clinical Trial Essential Documentation(21)


6/24/2013
Principal Investigator Training: Roles and Responsibilities(2)


6/25/2013
Trial Master Files: Why They Are Important & How to Organize Workshop(2)


6/26/2013
Medical Device Development: U.S. and EU Differences


6/26/2013
Data Privacy: Global Regulations and Expectations


6/27/2013
How to Write Effective Monitoring Reports and Communications Workshop(2)


6/28/2013
Adverse Event Monitoring for CRAs(9)