Drug Manufacturing Inspection Part III

Instructor: Vanessa Lopez
Product ID: 706259
Training Level: Basic
  • 19
  • December 2019
    Thursday
  • 10:00 AM PST | 01:00 PM EST
    Duration: 120 Min
Attend this course to prepare for and understand what will happen during a Drug Manufacturing Inspection for Surveillance Inspections. It will explain the FDA criteria to perform a For Cause Inspection.

Live Online Training
December 19, Thursday 10:00 AM PST | 01:00 PM EST | Duration: 120 Min

$299.00
One Dial-in One Attendee
$649.00
Group-Max. 10 Attendees/Location
(For Multiple Locations Contact Customer Care)
Super Deal - Get CD/USB Drive Free!

recorded version

$349.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section 48 hrs after completion of Live training

Training CD / USB Drive

$449.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days after completion of Live training

Combo Offers

Live + Recorded Version

$449.00

Live + Training CD/USB

$549.00

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

Why Should You Attend:

Inspections by the FDA can be challenging and there are consequences if you do not meet the requirements. This is a detailed course designed to provide pharmaceutical professionals with the information they require, in order to prepare for and understand what will happen during a Drug Manufacturing Inspection (Compliance Program 7356.002) for Surveillance Inspections and it will explain the FDA criteria to perform a For Cause Inspection. For your awareness, it will detail what will the FDA look for during Surveillance Inspections, the purpose and types of Surveillance Inspections, and who selects which systems will be covered during an inspection. Furthermore, it will go into in depth information on what will the FDA inspect for each system, and common deficiencies related in each of the systems.

Note: This webinar requires a pre-requisite webinar titled, "FDA Inspections: Understanding the Core Elements – Part I"

Learning Objectives:

This course will provide you with the system wide controls the FDA requires from the regulated pharmaceutical industry as they will verify through Surveillance Inspections. It will also explain the purpose and strategy they use for these inspections. You will learn each detailed element they will cover for each system, during the referred inspection, and when do each type of surveillance inspection apply.

Areas Covered in the Webinar:

The following topics will be addressed during this webinar:

  • Background
  • Objectives and Strategy Related to the Compliance Program 7356.002
  • Strategy Related to the Compliance Program 7356.002
  • Scheme of Systems for the Manufacture of Drugs/Drug Products
  • Program Management
  • Investigational Operations
  • Analytical
  • Typical Deficiencies Found as a Result of Systems Inspected

Who Will Benefit:

  • Quality Auditors
  • Compliance Officers
  • Managers/Directors/Supervisors and Personnel Related to:
    • Regulatory Compliance
    • Regulatory Affairs
    • Quality Control
    • Quality Assurance
    • Research and Development
    • Project Management
    • Production/Manufacturing
    • Risk Management
    • Complaint Handling
    • Personnel who are new to the regulated industry
    • Document Control
      Instructor Profile:
      Vanessa Lopez

      Vanessa Lopez
      Sr Quality Regulatory Consultant, Quality and Regulatory Consulting Services

      Ms. Lopez has held a wide variety of leadership roles in the Medical Device (Class: I, II, and III), Pharmaceutical (API; Finished Product) and Environmental regulated industries as well as the Consulting Services industry. She has worked for Edwards LifeSciences, Roche Diagnostics, Eli Lilly, Pall LifeSciences, among others. She possesses over 25 years of experience focused on development, implementation, driving improvements and monitoring of Quality Assurance, Quality Control, Regulatory Compliance, Regulatory Affairs, Quality Systems and Supplier Quality activities. Ms. Lopez has in-depth knowledge, coaches on interpretation and application of US regulations, EU directives, specific country regulations (Japan, Canada, and others), national/international standards and guidance documents. She has also held positions within the CAPA, Material, Safety and Management Review Boards as well as represented Quality in Design Control phases.

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Seminars by Ex-FDA Officials

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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