Online Quality, Compliance & Professional Development Courses
Looking for online training, professional development or certification in quality management, regulatory compliance and auditing? The courses and training bundles below cover ISO standards, FDA regulations, quality systems, auditing, statistical process control and other topics relevant to professionals working in regulated and quality-focused industries.
Select a course or training bundle below to learn more about the subject, course content and certification requirements.
ISO Standards & Quality Management Systems
ISO 9001:2026 Quality Management Systems — Requirements, Application and Auditing
Build a practical understanding of ISO 9001:2026 and the requirements behind an effective Quality Management System. The course covers the standard’s requirements, their application within an organization, and important auditing concepts for quality professionals, managers and auditors.
ISO 13485:2016 Medical Devices — Quality Management Systems — Requirements for Regulatory Purposes
Learn the quality management system requirements of ISO 13485 for organizations involved with medical devices. The course is particularly relevant to professionals working in medical device quality, regulatory affairs, manufacturing, auditing and compliance.
ISO 14001:2026 Environmental Management Systems
Explore the requirements and practical application of ISO 14001 for Environmental Management Systems, including environmental responsibilities, risks and opportunities, performance evaluation and continual improvement.
ISO 22442-1:2020 Medical Devices Utilizing Animal Tissues and Their Derivatives
Focused training covering medical devices that utilize animal tissues or derivatives, including risk management and the specialized quality and regulatory considerations associated with these materials.
Auditing Training
ISO 19011:2016 Guidelines for Auditing Management Systems
Develop a practical understanding of how management system audits are planned, conducted, documented and followed up. This training is relevant to internal auditors, quality professionals, compliance personnel and professionals taking on greater auditing responsibilities.
FDA & 21 CFR Compliance Training
21 CFR Part 11 — Electronic Records; Electronic Signatures
Learn FDA requirements governing electronic records and electronic signatures in regulated environments. The course is particularly relevant to quality, regulatory, validation, laboratory, IT and compliance professionals.
21 CFR Part 1271 — Human Cells, Tissues, and Cellular and Tissue-Based Products
Understand important FDA requirements affecting human cells, tissues, and cellular and tissue-based products (HCT/Ps), including topics relevant to tissue banking, biologics, cellular therapies and quality systems.
21 CFR Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals
Learn Current Good Manufacturing Practice requirements applicable to finished pharmaceuticals, with training relevant to pharmaceutical manufacturing, quality assurance, quality control, laboratory operations and regulatory compliance.
21 CFR Part 210 — Current Good Manufacturing Practice
Build a foundation in the FDA’s general Current Good Manufacturing Practice requirements for manufacturing, processing, packing and holding drugs.
21 CFR Part 820 — Quality System Regulation
Explore FDA quality system requirements associated with medical device manufacturing and their relevance to professionals working in quality, manufacturing, engineering, regulatory affairs and compliance.
Statistical Quality & Process Control
Using and Interpreting Control Charts for Continuous Process Monitoring
Learn how control charts and Statistical Process Control can be used to monitor processes, recognize meaningful variation and out-of-control conditions, and support better quality and process decisions.
Fundamentals of Sampling Plans
Develop a practical understanding of sampling plans and their role in quality control and acceptance decisions, including the application of statistically valid sampling within manufacturing, inspection and regulated quality systems.
Lead Auditor Training & Certification Bundles
The following training bundles combine subject-specific ISO or FDA regulatory training with ISO 19011 management system auditing training. Each provides a structured path for developing both subject-matter knowledge and auditing skills, with a specialized Lead Auditor certificate available upon successful completion of the required courses.
ISO 9001:2026 — Lead Auditor
Combines ISO 9001:2026 Quality Management Systems training with ISO 19011 auditing guidance, covering both QMS requirements and the principles used to plan, conduct and report management system audits.
ISO 14001:2026 — Lead Auditor
Combines ISO 14001 Environmental Management Systems training with ISO 19011 auditing guidance for professionals involved in environmental management, compliance and auditing.
ISO 13485:2016 — Lead Auditor
Combines ISO 13485 medical device Quality Management System requirements with ISO 19011 auditing principles for professionals who need both medical device quality knowledge and auditing skills.
21 CFR Part 11 — Lead Auditor
Combines training in FDA electronic records and electronic signature requirements with ISO 19011 auditing principles for professionals working with computerized systems and electronic quality records.
21 CFR Part 1271 — Lead Auditor
Combines regulatory training for human cells, tissues, and cellular and tissue-based products with professional auditing guidance for quality and compliance professionals in tissue, biologics and related regulated environments.
21 CFR Part 211 — Lead Auditor
Combines pharmaceutical Current Good Manufacturing Practice training with ISO 19011 auditing principles for professionals seeking greater knowledge of pharmaceutical compliance and auditing.
Frequently Asked Questions
The online training and professional development courses cover topics relevant to quality assurance, quality control, regulatory affairs, compliance, manufacturing, engineering, auditing, laboratory operations, process improvement and other technical and regulated professions.
Yes. The courses are delivered online and are self-paced, allowing professionals to complete training around their existing work and personal schedules.
Yes. A personalized certificate is available after successful completion of the applicable course requirements and assessments.
Available training includes ISO 9001 quality management systems, ISO 13485 medical device quality management systems, ISO 14001 environmental management systems, ISO 19011 management system auditing and ISO 22442-1 training for medical devices utilizing animal tissues and their derivatives.
FDA regulatory training includes 21 CFR Part 11, 21 CFR Part 1271, 21 CFR Part 210, 21 CFR Part 211 and 21 CFR Part 820. These courses cover subjects including electronic records, human cells and tissues, pharmaceutical Current Good Manufacturing Practice and medical device quality systems.
Lead Auditor bundles combine subject-specific ISO or FDA regulatory training with ISO 19011 auditing training. This provides both specialized subject knowledge and training in the principles and practices used to conduct management system audits. Available options include Lead Auditor training for ISO 9001, ISO 14001, ISO 13485, 21 CFR Part 11, 21 CFR Part 1271 and 21 CFR Part 211.
Yes. After successfully completing the required training, eligible trainees can receive the individual course certificates as well as the specialized Lead Auditor certificate associated with the bundle. Available options include the ISO 9001:2026 Lead Auditor, ISO 14001:2026 Lead Auditor, ISO 13485:2016 Lead Auditor, 21 CFR Part 11 Lead Auditor, 21 CFR Part 1271 Lead Auditor and 21 CFR Part 211 Lead Auditor training bundles.
Yes. Available professional development training includes Using and Interpreting Control Charts for Continuous Process Monitoring and Fundamentals of Sampling Plans. These topics are useful in manufacturing, inspection, quality control and process improvement environments.
No. A training certificate documents an individual’s successful completion of professional training. Organizational ISO certification is a separate process involving evaluation of an organization’s management system by an appropriate certification body.
Start with the ISO standard, FDA regulation or quality topic applicable to your responsibilities or professional development goals. If specific training is required by an employer, customer or regulatory program, confirm those requirements before selecting a course. You can also browse all available online courses to compare training topics.