2018 - Seminar on Hosting FDA Regulatory Inspections in San Diego

Course "Hosting FDA Regulatory Inspections" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Description:
Why you should attend:
The course will go through what typically goes on during an FDA inspection and will then cover how to prepare for, host and follow up to a regulatory inspection. It will focus the things that you should do or not do during the inspection. Typically FDA inspections can be highly structured and there are usually procedures that are to be followed. It is important for anyone who might be involved in the inspection to be aware of these procedures.
The course will also provide information for inspections conducted by international agencies as well as non- FDA agencies, including self inspections for manufacturing. It will explain how to prepare for an inspection, how to handle a scheduled or non-scheduled inspection, what to expect during an inspection and what follow up to expect after an inspection.
Finally, the course will provide information on how to respond to issues that come up during inspections and what to do to ensure best outcome from the inspection.
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Who will benefit:
Anyone who would be involved in the trial
• Regulatory Affairs professionals
• Quality Assurance
• Physicians
• Nurses
• Lab Technicians
• Operations
• Clinical Data Management
• Laboratory Management
• Manufacturing
• IT
Agenda:
Day 1 Schedule
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Lecture 1: FDA Inspections: FDA Inspection Program Overview
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Lecture 2: FDA Inspections: Key factors for a successful FDA inspection
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Lecture 3: FDA Inspections: Quality System Readiness
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Lecture 4: FDA Inspections: Information Readiness
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Lecture 5: FDA Inspections: Organization Readiness
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Lecture 6: FDA Inspections: Manage Inspection Outcomes
Day 2 Schedule
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Lecture 1: FDA Inspections: Managing Regulatory Risk
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Lecture 2: FDA Inspections: Food Facility Inspections
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Lecture 3: FDA Inspections: Medical Device Inspections
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Lecture 4: FDA Inspections: 21 CFR 11 Inspections
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Lecture 5: FDA Inspections: FDA Quality Metrics
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Lecture 6: FDA Inspections: CAPA
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Lecture 7: FDA Inspections: Writing Effective SOPs
Speaker:
Angela Bazigos
CEO, Touchstone Technologies Silicon Valley
Seasoned Executive with 40 years of experience in the Life Sciences & Healthcare Industries. Positions include Chief Compliance Officer. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Turnarounds and Business Development. Past employers / clients include Roche, Novartis, Genentech & PriceWaterhouseCoopers. Co-authored & prototyped 21 CFR 11 guidance with FDA.
Location: San Diego, CA Date: September 20th & 21st, 2018 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON
Price:
Register now and save $200. (Early Bird)
Until August 20, Early Bird Price: $1,295.00
From August 21 to September 18, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/spon...
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson-AT-globalcompliancepanel.com
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Registration Link - https://www.globalcompliancepanel.com/control/glob...
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