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FDA Utilization of Patient Preference Information in Regulatory Development & Decision Making Lifecycle Management: Updates and Insight on Post-Approval Changes, ICH Q12 Guidance and PAC iAM Activities Implementing MHRA’s New Guidance for Own Brand Labelling or ”Virtual Manufacturers”
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
Reinforcing Quality Management Systems through Greater Alignment of ISO 13485:2016 & the EU MDR Practical Methods for Strengthening Risk Management Practices in Medical Device Sourcing Opportunities in the Asc to Navigate the Future of Medical Device Reimbursement - Value Based Contracting Strategies
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
Case Study: First-Time Quality: Guiding a Contract Manufacturer to Eliminate Defects at the Source Insight into Medical Device Registrations in Latin America: Brazil & Mexico FDA MDR Enforcement Actions: Best Practices for Strengthening MedWatch Form Writing and Reporting
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00