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.
What differentiates our FDA Compliance Training?
- We provide exceptional, value-added, cost-effective, easily accessible Web-based Online On Demand FDA Compliance Training™ (available for 90 days from the purchase date).
- Our training content is developed by FDA Compliance Specialists with over 15 years of FDA regulated quality and compliance experience.
- Our training is deployed on a secure, reliable, Learning Management System, powered by Sun Enterprise servers, located in a secure facility, with redundant hardware, power, and internet connections.
- Our Learning Management System is easy to use and offers the flexibility to train anytime, anywhere, as long as you have a standard internet browser.
- To ensure each participant is sufficiently trained and our training is effective, there are test questions for each training module. Upon successful completion of the course, a Training Certificate is provided as documented evidence for your training records.
- Why pay extra money for membership fees?
- Why pay extra money for third party training
certification that is not required by the FDA? - Why pay extra money for expensive reference
books that are not required by the FDA? - Why pay extra money for exam preparation
materials that are not required by the FDA? - Why pay extra money to take the exam?
- Why pay extra money to re-take the exam if you
fail to pass the exam? - Why pay extra money for airfare, car rental, and
hotel expenses to attend training? - Why pay extra money for inferior content?
Who should take FDA Compliance Training?
All employees, contractors, consultants, and suppliers currently supporting or wanting to support FDA cGMP audit program activities:
- Directors, Managers, Supervisors
- Engineers
- Auditors
- Manufacturing personnel
- Quality Control personnel
- Quality Assurance personnel
- Quality Management personnel
- Corporate personnel
- Laboratory personnel
- Equipment personnel
- Warehouse, Holding and Distribution personnel
- Personnel supporting the control of components and drug product containers and closures
- Packaging and labeling personnel
- Contractors, consultants, and suppliers
Course Instructor:
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.
FDA Compliance Specialists on Demand:
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!
FDA Compliance Specialist:
Certified cGMP Quality Auditor™
Online On Demand Training, Click Here!
Pricing: $1,500.00 per person
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Pre-requisites for this course are:
- Current Good Manufacturing Practice (cGMP) Training
(21 CFR Part 210 and 21 CFR Part 211)
- Good Documentation Practices (GDP) Training.
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.
Course Content:
| • | 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 methods. |
| • | 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 criteria. |
| • | Module 12: | Understand audit scheduling, pre- audit requests and activities, audit preparation, audit logistics, and coordination. |
| • | Module 13: | Understand the audit notification Letter. |
| • | 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 effectiveness. |
| • | Module 18: | Understand how to conduct an opening meeting, audit management, and establishing transparent communication. |
| • | 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 conflict resolution. |
| • | Module 23: | Understand how to document clear, complete, defendable audit observations with objective documented evidence. |
| • | 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 requirements. |
| • | 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 report. |
| • | 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 closure. |
| • | Module 37: | File retention and audit metrics. |
Certifications:
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?
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.
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:
- Up to 10 Users
- Up to 25 Users
- Up to 50 Users
- Up to 100 Users
- Up to 200 Users
- 300 Users or more