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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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September 22, 2010 |
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GlobalCompliancePanel, Online Training Webinar
2010-10-12
Areas Covered in the Session: - QSR and ISO 13485 requirements for document control
- Description of typical document control system in use
- Streamlined document control process
- Paper-free document review
- Immediate document distribution
- Paper-free document management system
Who Will Benefit: This webinar will provide valuable assistance to all regulated companies, since a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include: - Executive Management
- Document Control Management
- Document Control Clerks
- Consultants
- Quality system auditors
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Organized by:
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GlobalCompliancePanel |
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Invited Speakers:
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Jeff Kasoff, RAC, is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. Jeff is responsible for oversight of corporate compliance with domestic and international regulations, preparation of submissions, and is primary liaison with regulatory agencies and notified bodies. Jeff has presented dozens of webinars in many areas dealing with regulatory compliance. Jeff began his regulatory career as the first full-time employee of Optex Biomedical, a device start-up, where he initiated their regulatory policies and procedures and prepared their submissions. Jeff received his Regulatory Affairs Certification in 1996.
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Deadline for Abstracts:
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2010-10-11
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Registration:
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Live live online training only for one participant Price: $245.00 | Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care) | | |
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E-mail:
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webinars@GlobalCompliancePanel.com
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