CSQ CERTIFICATION
The CSQ Certification Program and applicable standards were built around ISO/IEC 17067
Globally Recognized · Live Training
cGMP V2.0 Training
100% Live & Interactive
Join our live virtual cGMP V2.0 training led by an experienced industry expert. Ask questions in real time, build practical cGMP knowledge, and leave audit-ready.
★★★★★
"Stay ahead of evolving compliance standards with Kiwa ASI's official cGMP V2.0 Training. This 8-hour live course gives you a thorough, practical understanding of Current Good Manufacturing Practices aligned with cGMP V2.0 requirements."
All Materials IncludedCertificate Included
Kiwa ASI
cGMP 2.0 Training
Stay ahead of evolving compliance standards with Kiwa ASI's official cGMP V2.0 Training. This 8-hour live course gives you a thorough, practical understanding of Current Good Manufacturing Practices aligned with cGMP V2.0 requirements. Whether you're building a foundation or updating your knowledge, this training prepares you to implement cGMP standards confidently in day-to-day operations.
8
Contact Hours
Live
Virtual via Zoom
V2.0
Updated cGMP Curriculum
Audit
Ready
Upcoming Dates — $299 per seat
Need to train 6+ people? Ask about on-site private training →
What You'll Learn
Complete Training Curriculum
Day 1
8:30 AM – 4:30 PM CT
8 contact hours
8 contact hours
Program Overview & Key Regulatory Updates
The Kiwa ASI cGMP V2.0 Training is a comprehensive 8-hour course designed to provide participants with an up-to-date understanding of Current Good Manufacturing Practices (GMP) in accordance with cGMP V2.0 standards. This training focuses on building a strong foundation in cGMP principles while emphasizing practical application, compliance, and quality excellence in regulated manufacturing environments.
The course covers key areas such as quality management systems, documentation and record control, personnel responsibilities, facility and equipment requirements, deviation management, CAPA, data integrity, and audit/inspection readiness. Through practical examples and real-world scenarios, participants will learn how to effectively implement Kiwa ASI cGMP V2.0 requirements in daily operations and maintain continuous compliance.
- Quality management systems
- Documentation and record control
- Personnel responsibilities
- Facility and equipment requirements
- Deviation management
- CAPA
- Data integrity
- Audit and inspection readiness
Your Instructor
Harmeet Kaur
Director of Training & Consulting Services, Kiwa ASI
Harmeet brings nearly two decades of food safety consulting and training experience to every class. She has worked with companies ranging from small startups to multinational corporations, helping them navigate regulatory compliance, quality systems, and audit readiness.
As a certified lead instructor and approved training partner, Harmeet combines deep technical knowledge with practical, real-world insight. She takes a collaborative approach, working closely with clients to develop customized solutions — from HACCP plans and FDA Food Safety Plans to internal audits and staff training.
- Lead Instructor
- Approved Training Partner
- Certified Trainer & Consultant
- M.S. Food Science
Frequently Asked Questions About cGMP V2.0 Training
What is cGMP V2.0 training?
Kiwa ASI cGMP V2.0 Training is a live, 8-hour virtual course covering Current Good Manufacturing Practices in accordance with cGMP V2.0 requirements. It builds a strong foundation in cGMP principles with an emphasis on practical application, compliance, and quality excellence in regulated manufacturing environments.
Who should attend?
Quality, production, sanitation, and supervisory personnel in food, packaging, dietary supplement, and other regulated manufacturing facilities — whether you are building a foundation in cGMP or updating your knowledge to the V2.0 requirements.
How long is the course and what is the format?
The course is 8 contact hours delivered in one full-day live session (8:30 AM – 4:30 PM CT) via Zoom. Sessions are led by an experienced industry expert in real time, so you can ask questions about your own products and processes.
What topics are covered?
Quality management systems, documentation and record control, personnel responsibilities, facility and equipment requirements, deviation management, CAPA, data integrity, and audit/inspection readiness — all illustrated with practical examples and real-world scenarios.
How much does the course cost?
$299 per seat. This includes all course materials, live instructor access, and a certificate of completion. Group pricing is available for organizations training six or more — contact US.Info@kiwa-asi.com or call 1 (800) 477-0778.
Do I receive a certificate?
Yes. Participants who complete the full 8-hour session receive a Kiwa ASI cGMP V2.0 Training certificate, which can be used as documented evidence of training for audits and inspections.
Can I reschedule if I can’t attend?
Yes. Contact Kiwa ASI at US.Info@kiwa-asi.com or call 1 (800) 477-0778 to reschedule at no additional charge. Refunds are available up to 5 business days before the course start date.
Does Kiwa ASI offer on-site cGMP training?
Yes. For organizations training six or more people, Kiwa ASI offers on-site private cGMP training customized to your specific products, processes, and regulatory requirements. Contact US.Info@kiwa-asi.com or call 1 (800) 477-0778 for group pricing and scheduling.
Training six or more people?
On-site private cGMP training can be customized to your specific products, processes, and regulatory requirements. Call 1 (800) 477-0778 or email US.Info@kiwa-asi.com.
All consulting services are offered through ASI Training and Consulting, LLC. All activity is conducted separately from our accredited certification body, ASI Food Safety, LLC, in order to safeguard against any conflicts of interest.