2-day In-person Seminar

Hosting FDA Regulatory Inspections


September 20th & 21st, 2018

Time: 9:00 AM to 6:00 PM

San Diego, CA

Venue: DoubleTree by Hilton San Diego Downtown


Director : Angela Bazigos

**Please note the registration will be closed 2 days (48 Hours) prior to the date of the seminar.

  Price: $1,495.00
(Seminar Fee for One Delegate)

  Register for 5 attendees   Price: $4,485.00
      $7,475.00 You Save: $2,990.00 (40%)*

  Register for 10 attendees   Price: $8,222.00
      $14,950.00 You Save: $6,728.00 (45%)*
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.

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.


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

Day 1 Schedule


Lecture 1: FDA Inspections: FDA Inspection Program Overview


Lecture 2: FDA Inspections: Key factors for a successful FDA inspection


Lecture 3: FDA Inspections: Quality System Readiness


Lecture 4: FDA Inspections: Information Readiness


Lecture 5: FDA Inspections: Organization Readiness


Lecture 6: FDA Inspections: Manage Inspection Outcomes


Day 2 Schedule


Lecture 1: FDA Inspections: Managing Regulatory Risk


Lecture 2: FDA Inspections: Food Facility Inspections


Lecture 3: FDA Inspections: Medical Device Inspections


Lecture 4: FDA Inspections: 21 CFR 11 Inspections


Lecture 5: FDA Inspections: FDA Quality Metrics


Lecture 6: FDA Inspections: CAPA


Lecture 7: FDA Inspections: Writing Effective SOPs


Want to register by P.O/Check?
We facilitate registration by P.O/Checks!
Complete your registration in just a few easy steps
Please just download, fill out the registration form and send it to us either by email to support@globalcompliancepanel.com or just fax us at 302 288 6884.
Once the form is received, an invoice will be generated and sent back to your fax number.
Following this just send us your purchase order by fax at 302 288 6884
Click here to download Registration form
In case you wish to register by using check
In case you wish to register by using check, please make a check to NetZealous LLC DBA GlobalCompliancePanel.com and mail it to the below address.
NetZealous LLC,
DBA GlobalCompliancePanel,
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA
Phone: 1800 447 9407

Want to register by Wire Transfer?
Please call any of our representatives on 1800 447 9407 to help you completed the transfer.
Group participations
Get fabulous discounts by participating in groups of two or more.
No Attendees Discount
1 2 Attendees 10% off
2 3 to 6 Attendees 20% off
3 7 to 10 Attendees 25% off
4 10+ Attendees 30% off

To avail the above group discounts, all the participants should register by making a single payment

Call our representative TODAY on 1800 447 9407 to have your seats confirmed!

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 http://morflearning.com/angelabazigos/. 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. Co-authored Computerized Systems in Clinical Research w/ FDA http://www1.diahome.org/~/media/4FA562336EBD46C58CDC43A8B7773095.ashx Patent on speeding up software compliance https://www.google.com/patents/US8266578. Recently quoted in Wall Street Journal for using training to bring regulatory compliance to the Boardroom http://blogs.wsj.com/riskandcompliance/2015/07/24/using-training-to-bring-compliance-to-boardrooms/ National Trainer for Society of Quality Assurance. Comments / collaborates with FDA on new guidance documents. Former President of Pacific Regional Chapter of Society of Quality Assurance. Stanford's Who's Who for LifeSciences: http://www.stanfordwhoswho.com/Angela.Bazigos.7144112.html#overview.

Location: San Diego, CA Hotel: DoubleTree by Hilton San Diego Downtown   1646 Front St, San Diego, CA 92101, USA



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