With global health concerns and technological innovations shining a light on the life sciences, MasterControl, MedTech Association and MASSMedic are joining forces to offer a series of informative webinars targeted to companies that might be new to or would like more education on the fundamentals of manufacturing in the sector. In a series of 10 episodes divided between four sessions, expert presenters will cover the quality processes and regulatory steps required for success in life sciences manufacturing.
These webinars may qualify for education credits, please check with your association to verify and MasterControl will provide a certificate of attendance.
The comprehensive 10-part series is broken into four sessions that cover the full spectrum of essential manufacturing-focused subjects.
Register today to sign up for all four sessions. If you cannot attend all four sessions, you can still register to receive links to on-demand viewing.
SESSION 1: July 21, 2020: 1 p.m. - 2 p.m. EDT
Episode 1: An Introduction to Quality Management System (QMS) for Regulated Industry – Next Steps
Episode 2: Elevate Your QMS
SESSION 2: August 4, 2020: 1 p.m. - 2 p.m. EDT
Episode 3: Achieving and Maintaining an Audit-Ready State
Episode 4: ISO vs. cGMP vs. FDA Requirements.
Episode 5: FDA Current Guidance and Exemptions.
SESSION 3: August 18, 2020: 1 p.m. - 2 p.m. EDT
Episode 6: Documentation – Standard Operating Procedures (SOPs) and Work Instructions.
Episode 7: Documentation – Batch and Design History Records.
Episode 8: Documentation – Quality Event Management and Audit.
SESSION 4: September 1, 2020: 1 p.m. - 2 p.m. EDT
Episode 9: Future Proofing – Continuing Production Beyond Exemption.
Episode 10: Future Proofing – Digital Production Records, QMS and Validation.