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Medical Device Quality Improvement: Implementing Postmarket Cybersecurity Programs Aligned with New FDA Guidelines Best Practices for Medical Device Reporting (MDR) Under FDA’s Final Guidance 13485 2016 – Integrating Changes to Develop a Comprehensive Quality Management System
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
HRSA Final Rule for 340B- New Requirements for Calculating Ceiling Prices & the New Reality of Civil Monetary Penalties Effective Strategies for Medical Writing Project Management Overcoming Complexity in Meeting CMC Regulatory Requirements for Drug-Led Combination Products
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Our Price: $395.00
Our Price: $395.00
CMC Case Study: Best Practices in FDA Meeting Preparation Strategies Status Update- MDR Surprises and Key Regulatory Developments Software as a Medical Device (SaMD): Clinical Evaluation- New Guidance from FDA and Global Regulators
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00