WHY TRAIN WITH VELOCITY 360?
Velocity 360 training products are developed within our ISO 9001:2015 quality management system, certified by NQA, an ANAB-accredited certification body. We are also an Exemplar Global Certified Training Provider for select training programs.
This four-course program develops practical competencies for auditing pharmaceutical quality systems against FDA 21 CFR Parts 210 and 211 and ISO 13485, applying ISO 31000 risk management principles, strengthening documentation and data integrity, and using FMEA to control product and process risks.
Designed for pharmaceutical quality managers, internal auditors, regulatory professionals, engineers, manufacturing personnel, and compliance professionals responsible for CGMP operations, controlled documentation, risk-based decision-making, and audit readiness.
This On-Demand, 32-hour e-course provides practical instruction in FDA 21 CFR Parts 210 and 211 pharmaceutical CGMP requirements, ISO 13485, and ISO 19011 internal auditing guidance. Includes a Certificate of Competence. 3.2 CEUs. Language: English.
This On-Demand, 6-hour e-course provides practical instruction in the ISO 31000:2018 principles, framework, and process for managing organizational risk. Includes a Certificate of Competence. 0.6 CEUs. Language: English.
This On-Demand, 4-hour e-course provides practical instruction in Good Documentation Practice and the ALCOA+ principles of data integrity. Includes a Certificate of Competence. 0.4 CEUs. Language: English.
This On-Demand, 4-hour e-course provides practical instruction in the seven-step FMEA methodology, risk analysis, rating criteria, Action Priority, and auditing FMEA effectiveness. Includes a Certificate of Competence. 0.4 CEUs. Language: English.
