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Webinar On Good Documentation Practices for Clinical Trials

20 February 2015, Mississauga, Canada


Introduction
Description :

In this 60-min webinar, you will have unparalleled opportunities to bring great value and benefits to your organization and to greatly improve your GCPs with increased awareness of the needs - sustainable compliance and patient safety.

Areas Covered in the Session :
Statutes, Regulations and Definitions
Regulatory Requirements for INDs and IDEs.
Clinical Trials
Clinical Investigators (CI)
Institutional Review Boards (IRBs)
Sponsors and Monitors
Contract Research Organizations (CROs)
ICH-GCP Guidelines
ISO 14155
List of SOPs and Adequate Documentation
Key Elements in the SOPs
Common GCP Deficiencies in EU and US
Enforcement Actions
Lessons Learned

Who Will Benefit:
Clinical Affairs
Regulatory Affairs
Quality Assurance
Research & Development
Consultants
Contractors/Subcontractors
Senior Management
Anyone Interested in the Topic

Price Tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299

For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com

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Online

Compliance Trainings, Online, 5939 Candlebrook Ct, Ontario, Mississauga, L5V 2V5, Canada

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Organised by
Compliance Trainings is the global organization for regulatory affairs professionals for those who have an interest in regulatory affairs in Food, drugs, Biologics, Medical, Healthcare, HR, IT sectors.
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