Chasing Compliance: The Global Regulatory Podcast

RAPS Convergence 2025 Review with Violet Chazovachii

18 Nov 2025

Contributed by Lukas

Welcome to Chasing Compliance, the GLOBAL regulatory podcast, where we discuss all aspects of medical device and pharmaceutical regulatory and clini...

Rushing vs. Readiness — The High Cost of a Clinical Hold on a Biologics IND

07 Oct 2025

Contributed by Lukas

Welcome to Chasing Compliance, the GLOBAL regulatory podcast, where we discuss all aspects of medical device and pharmaceutical regulatory and clinica...

Writing Great CSRs

26 Aug 2025

Contributed by Lukas

Welcome to Chasing Compliance, the Global Regulatory Writing and Consulting podcast where we discuss all aspects of medical device and pharmaceutical ...

Writing Excellent CERs

07 Jul 2025

Contributed by Lukas

Welcome to Chasing Compliance, the Global Regulatory Writing and Consulting podcast where we discuss all aspects of medical device and pharmaceutical ...

All About ADDM - New Technology To Manage Regulatory Communication Projects and Analyze Regulatory Feedback

22 Apr 2022

Contributed by Lukas

In this podcast we introduce one of Global’s latest ventures, the Global Regulatory Technology Operations (GRTO) team and discuss their newest appli...

Tips and Tricks for Performance Evaluation Reports (PERs)

21 Jan 2022

Contributed by Lukas

This episode of Chasing Compliance is for those working on regulatory submissions for in-vitro diagnostic (IVD) medial devices. Today we talk to our ...

Part 2 - Tips and Tricks for Technical Writing

23 Dec 2021

Contributed by Lukas

Ready to take your technical writing to the next level, but not sure where to start? Would you like to learn some tips to freshen up your writing app...

Part 1 - Tips and Tricks for Technical Writing

09 Dec 2021

Contributed by Lukas

Ready to take your technical writing to the next level, but not sure where to start? Would you like to learn some tips to freshen up your writing app...

Part 2 - Abbreviated New Drug Applications: Fundamentals, Challenges, and Agency Communication

24 Nov 2021

Contributed by Lukas

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 K...

Part 1 - Abbreviated New Drug Applications: Fundamentals, Challenges, and Agency Communication

08 Nov 2021

Contributed by Lukas

Chasing Compliance: The Global Regulatory Podcast kicks off season two with a two-part episode on abbreviated new drugs applications (ANDAs). Our gue...

Part 2 - Clinical Site Selection and Evaluation: Tips and Best Practices

15 Jul 2021

Contributed by Lukas

Welcome to clinical site selection and evaluation Part 2, where we continue the conversation on optimizing clinical site selection and evaluation. In...

Part 1 - Clinical Site Selection and Evaluation: Acceleration Through Effective Collaboration

15 Jun 2021

Contributed by Lukas

This is part 1 on our conversation on optimizing clinical site selection and evaluation. In this episode Linda Peterson and Julie Sheidy provide some...

Part 3 - Graduates of the The Global CER Internship Program Share Their Stories

11 May 2021

Contributed by Lukas

This episode of Chasing Compliance features two first-hand accounts of what it was like to participate in the Global Clinical Evaluation Report (CER)...

Introducing The Global Regulatory Writing and Consulting Blog

13 Apr 2021

Contributed by Lukas

We are excited to announce the launch of the official Global Regulatory and Consulting Blog. To celebrate the release of the first blog posts we are ...

Generic Pharmaceuticals: Development, Testing, and Regulation

26 Mar 2021

Contributed by Lukas

In this episode of Chasing Compliance, Jamie talks with Brandi Quinlin and Rebecca Lynch about generic drugs. The discussion ranges from what a gener...

Maximizing the Relationship with A Clinical Research Organization (CRO) - A Panel Discussion with Linda Peterson, Sarah Schaul, and Kari Gibney

08 Mar 2021

Contributed by Lukas

In this episode of Chasing Compliance, Linda Peterson, Sarah Schaul, and Kari Gibney discuss how to maximize the relationship with your CRO from the ...

Marysa Mezzetti - Risk Documentation and MDR

07 Oct 2020

Contributed by Lukas

Have you considered the impacts of the Medical Device Regulation (MDR) on your current risk documentation and management strategies? You may be w...

Part 2 - Overview of Global's CER Internship and Stories of Entering Regulatory Writing with Jacob Hoffman and Juliet Peña

05 Sep 2020

Contributed by Lukas

Part 1 - Overview of Global's CER Internship and Stories of Entering Regulatory Writing with Beth Meier and Dan Sheidy

05 Sep 2020

Contributed by Lukas

Sarra De Valence - Senior Manger of CER Writing on Systematic Literature Search and Screening

27 Aug 2020

Contributed by Lukas

On this episode of Chasing Compliance, host Jamie Hijmans and Sr. Manager Sarra De Velance discuss systematic literature search and screening. They d...

John Jolly - Manager of CER Writing Discusses Medical Device Post Market Surveillance (PMS)

07 Aug 2020

Contributed by Lukas

In this episode of Chasing Compliance, host Jamie Hijmans sits down with John Jolly, a Manager in Global’s Medical Device Department to discuss med...

Carrie Eklund - Senior Manager of CMC

20 Jul 2020

Contributed by Lukas

In this episode of Chasing Compliance, host Jamie Hijmans sits down with Carrie Eklund, Senior Manager of Chemistry, Manufacturing, and Controls or C...