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Chasing Compliance: The Global Regulatory Podcast
GLOBAL
21 episodes
1 month ago
Chasing Compliance, presented by Global Regulatory Writing & Consulting, is a podcast focused on regulatory strategy, achieving and maintaining regulatory compliance, and the influence of regulation on healthcare overall. Guests include highly accomplished regulatory professionals, medical writers, scientists, engineers, and clinicians giving their take on some of the most complicated and challenging topics in clinical development.
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Science
Business,
Government
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All content for Chasing Compliance: The Global Regulatory Podcast is the property of GLOBAL and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
Chasing Compliance, presented by Global Regulatory Writing & Consulting, is a podcast focused on regulatory strategy, achieving and maintaining regulatory compliance, and the influence of regulation on healthcare overall. Guests include highly accomplished regulatory professionals, medical writers, scientists, engineers, and clinicians giving their take on some of the most complicated and challenging topics in clinical development.
Show more...
Science
Business,
Government
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Part 2 - Abbreviated New Drug Applications: Fundamentals, Challenges, and Agency Communication
Chasing Compliance: The Global Regulatory Podcast
19 minutes 52 seconds
3 years ago
Part 2 - Abbreviated New Drug Applications: Fundamentals, Challenges, and Agency Communication
This episode is Part 2 of a two-part episode on Abbreviated New Drug Applications (ANDAs). We continue our conversation with our ANDA expert Sandra Kircus. In this part, Sandra provides advice on how to manage ANDA projects, the importance of strong project management, and provides suggestions for project management tools. She also shares her thoughts on how to regulatory leaders can optimize the ANDA writing process and how to optimize the ANDA process fro companies outside of the United States referred to as xUS companies. Sandra and Jamie discuss why having strong US agent for xUS companies is important. While this advice is focused on xUS companies, it also rings true for US companies as well. 2:30 – Tips for general approach to writing ANDAs Make sure you understand what the agency is looking forStay focused, don’t give the FDA more than they need or that they are asking for. The level of detail in your regulatory documentation doesn’t need to match the level of detail in your technical documentation. Give yourself flexibility. 5:40 – Tips for the ANDA writing process Put effort into the program management aspectMake sure all contributors and stakeholders are alignedHave periodic discussions with the teamGet 1:1 time with the team to discuss the project and specific sections 8:00 – Software for Program Management 10:30 – Proportion of applications from US companies and outside or xUS companies. Implications for xUS companies and role of US agents. 
Chasing Compliance: The Global Regulatory Podcast
Chasing Compliance, presented by Global Regulatory Writing & Consulting, is a podcast focused on regulatory strategy, achieving and maintaining regulatory compliance, and the influence of regulation on healthcare overall. Guests include highly accomplished regulatory professionals, medical writers, scientists, engineers, and clinicians giving their take on some of the most complicated and challenging topics in clinical development.