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 current good manufacturing practice systems, applying ISO 31000 risk management principles, strengthening documentation and data integrity, and using FMEA to identify and control product and process risks.
Designed for pharmaceutical quality, regulatory, manufacturing, validation, engineering, and compliance professionals responsible for GMP systems, audits, risk management, data integrity, and continual improvement.
This On-Demand, 40-hour e-course provides practical instruction in FDA 21 CFR Parts 210 and 211 pharmaceutical CGMP requirements, ISO 13485, and ISO 19011 lead auditing guidance. Includes a Certificate of Competence. 4.0 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.
This final certificate-issuance step follows successful completion of all prerequisite courses and program requirements. Completing the step issues a Certificate of Competence for GMP Pharma Certified Quality Manager.
Earn Five Secure, Digitally Verifiable Certificates
