Pharmaceutical, Medical Device, Biotechnology firms, and their supply chains are constantly seeking qualified personnel because they are dealing with dynamic corporate changes and regulatory compliance challenges to meet business demands. Highly regulated companies understand there is a strategic competitive advantage when they hire employees, consultants, and contractors with the education, training, and experience needed to facilitate corporate compliance, improve their overall on-the-job effectiveness, and mitigate compliance issues.
All employees, contractors, consultants, and suppliers currently supporting or wanting to support FDA cGMP audit program activities:
Our Web-based Online On Demand FDA Compliance Training™ is developed by highly credentialed industry experts who are uniquely qualified and average over 15 years of hands-on FDA regulated industry quality and compliance experience. Each of our instructors have held senior management positions working for some of the world’s most widely recognizable and trusted pharmaceutical, medical device or biotechnology life science organizations in the world. Each of our course Instructors have real-world experiences representing highly regulated firms during FDA inspections.
Our global cGMP, Medical Device, and Supplier Quality Auditing services are backed with a 100% money back guarantee. Simply put, if you’re not satisfied with the quality of our auditing services, we will refund your money. Call us Today!
Pricing: $1,500.00 per person
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Pre-requisites for this course are:
About the Course:
This Web-based Online On Demand FDA Compliance Training™ course (accessible for 90 days from the purchase date) provides a comprehensive overview and working knowledge of cGMP Quality Auditor Training. All phases of the audit process are covered to provide the knowledge, skills, and tools needed to be a cGMP Quality Auditor. The FDA requires that persons (employees, consultants, contractors) who provide support or use electronic record/electronic signature systems (in support of FDA GxP and QSR regulated activities) have the education, training, and experience to perform their assigned functions. Annual cGMP Quality Auditor training with effectiveness testing improves individual contributor working knowledge, skills, and effectiveness; helps to proactively reduce regulatory risks; and facilitates FDA compliance. Investing in FDA Compliance Training is essential to the qualifications, growth, and success of any individual wanting to support FDA regulated activities. All participants will receive a Certificate of Training upon successful completion.
|•||Module 1:||Audit terms and definitions.|
|•||Module 2:||Understand the different types of audits.|
|•||Module 3:||Understand the different phases
and activities of the quality system audit.
|•||Module 4:||Independence of the audit function.|
|•||Module 5:||Auditing principles, procedures, and
|•||Module 6:||Global pharmaceutical regulatory
enforcement bodies, international
standards, and guidance.
|•||Module 7:||Understand the audit team leader.|
|•||Module 8:||Understand the importance of selecting
the right audit team members.
|•||Module 9:||Roles and responsibilities of the
auditors and the auditee participants.
|•||Module 10:||Auditor conduct, professionalism,
personal behavior, and ethics.
|•||Module 11:||Understand the audit purpose, audit
scope, audit objectives, and audit
|•||Module 12:||Understand audit scheduling, pre-
audit requests and activities, audit
preparation, audit logistics, and
|•||Module 13:||Understand the audit notification
|•||Module 14:||Understand the audit plan, effective
resource utilization, and reviewing
the audit plan with the auditee.
|•||Module 15:||Understand the importance of
traceability with the audit report in
accordance with the audit plan.
|•||Module 16:||Understand audit checklists.|
|•||Module 17:||Understand the audit agenda for
|•||Module 18:||Understand how to conduct an
opening meeting, audit management,
and establishing transparent
|•||Module 19:||Conducting a site tour.|
|•||Module 20:||Sampling of records and documents
to verify cGMP compliance.
|•||Module 21:||Documenting the audit activities.|
|•||Module 22:||Conducting effective interviews and
|•||Module 23:||Understand how to document clear,
complete, defendable audit
observations with objective
|•||Module 24:||Understand the Pre-daily wrap-up
meeting with the audit team.
|•||Module 25:||Understand the daily wrap-up
meeting with the auditee.
|•||Module 26:||Understand the final audit debrief /
Close out for effectiveness.
meeting with auditee.
|•||Module 27:||Audit report development and
compliance with audit process
|•||Module 28:||Understand combining similar audit
observations for the audit report.
|•||Module 29:||Understand critical elements for
documenting defendable audit
observations on the audit report.
|•||Module 30:||Review and approval of the audit
|•||Module 31:||Confidentiality and controlled
distribution of the audit report.
|•||Module 32:||Audit certification.|
|•||Module 33:||Reviewing the audit response and
action plan for acceptance.
|•||Module 34:||CAPA management.|
|•||Module 35:||Revisit the auditee and follow-up.|
|•||Module 36:||Verification of audit response
action plan completion for audit
|•||Module 37:||File retention and audit metrics.|
We provide Web-based Online On Demand FDA Compliance TrainingTM certifications for employees, consultants, and contractors currently supporting or wanting to support FDA regulated activities for pharmaceutical, medical device, biotechnology, and related supply chain firms. All training course certifications have been developed by a committee of highly credentialed industry experts who are FDA Compliance Specialists and average over 15 years of hands-on FDA regulated industry quality and compliance experience. There is no formal application process and no extra cost above standard training course fees.
Frequently Asked Questions:
How do I register for an FDA Compliance Training course?
There are two ways to register for the training course.
You may click on Register
at the top of the page to enroll using a credit card via this website or, you may call our office at +1 (212) 884-0333 to enroll by telephone.
To register for a training course, you must pay for the course in full, or be approved for direct invoice. Payment in full is required before any Web-based Online On Demand FDA Compliance Training™ is provided.
After I register for a training course, how long will I have
to access the training course?
The Web-based Online On Demand FDA Compliance Training™ will be available for 90 days from the purchase date.
Do I need to download software to participate?
No. The training is provided by a secure, Online On Demand Web Based Learning Management System as long as you have a standard internet browser to access the course.
What is your cancellation policy?
Because of development and infrastructure costs, highly competitive pricing, and exceptional content that will be made available after the purchase, all Web-based Online On Demand FDA Compliance TrainingTM sales are final.
Do you offer discounts for group pricing?
Yes. Please contact us for special group discount pricing: