Laboratory & Technical Services
Strengthen your quality skills for laboratory and technical services with online training in quality management, statistical process control, sampling plans, and auditing. These self-paced courses help laboratory professionals, quality teams, and technical managers evaluate data, understand process variation, and support reliable results. Learn on your schedule and earn verifiable certificates of completion.
ISO 9001:2026 Quality management systems — Requirements, application, and auditing
Get a practical understanding of ISO 9001:2026 and learn how its requirements apply to real-world [...]
ISO 22442 Lead Auditor
Working with animal-derived materials in medical devices requires careful attention to safety, quality, and regulatory [...]
Animal Tissue Specialist
Working with animal-derived materials in medical devices requires a thorough understanding of quality, safety, and [...]
ISO 14001:2026 Environmental management systems – Requirements with guidance for use. Requirements, application, and auditing.
Build your understanding of environmental management with this self-paced ISO 14001:2026 course. You’ll learn how [...]
21 CFR Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General
Get a clear introduction to the FDA’s current good manufacturing practice (cGMP) requirements for drugs. [...]
21 CFR Part 1271 Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)
Understand the FDA requirements for human cells, tissues, and cellular and tissue-based products (HCT/Ps). This [...]
ISO 13485:2016 – Medical Devices — Quality Management Systems — Requirements for Regulatory Purposes
Requirements, Application, and Auditing Build your understanding of medical device quality management with this self-paced [...]
ISO 19011:2016 Guidelines for Auditing Management Systems
Build your confidence in auditing management systems with this ISO 19011 course. You’ll explore how [...]
21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals
Build your knowledge of the FDA’s current good manufacturing practice (cGMP) requirements for finished pharmaceuticals. [...]


