Welcome to Chasing Compliance, the GLOBAL regulatory podcast, where we discuss all aspects of medical device and pharmaceutical regulatory and clinical strategy – from bench to bedside.

Today we are chatting with Violet Chazovachii. Violet has spent almost a decade in the biomedical technology field. As a graduate researcher at the University of Michigan Ann Arbor, she focused on developing surface coatings to optimize microparticles for vascular targeted drug delivery. After earning her master’s degree, she joined Global’s CER internship program in 2021 and has advanced to the role of Lead Medical Writer, where she continues to contribute to high-impact regulatory submissions. Violet recently earned her RAC (Regulatory Affairs Certification) in Medical Devices

Thank you for being here Violet! On this episode, we are discussing RAPS convergence 2025. We sent a team to this conference and had a wonderful experience connecting with regulatory affairs peers and learning the latest developments and trends in US and global healthcare regulations. Violet was one of our teammates on the ground and has some great insights from the week. Let’s dive in!

Welcome to Chasing Compliance, the GLOBAL regulatory podcast, where we discuss all aspects of medical device and pharmaceutical regulatory and clinical strategy – from bench to bedside.

Today we are chatting with Julie Matison and Scott Michaels.

Julie Matison holds a Bachelor’s degree in Chemical Engineering and a Master’s degree in Mechanical Engineering, and recently earned the RAC-Drugs certification through RAPS. She has over 21 years of experience in the pharmaceutical industry, with a strong background in manufacturing, validation and quality.

Scott Michaels earned his Master’s in Pharmaceutical Chemistry from the University of Kansas and his Bachelor’s in Chemistry from McGill University. He has held a variety of regulatory and CMC product development roles over the past 20 years, working with both small molecules and biologics.

Thank you both for being here! On this episode, we are discussing CMC strategy around biologics IND submissions. I am sure our audience is looking forward to your insights, so let’s dive in.

Welcome to Chasing Compliance, the Global Regulatory Writing and Consulting podcast where we discuss all aspects of medical device and pharmaceutical regulatory and clinical strategy from bench to bedside. Today we are chatting with Eimile Oakes and Andrew Stephens, discussing Clinical Study Reports, also known as CSRs. CSRs must tell a clear, compliant, and credible story of a clinical trial. With so many moving parts and often tight timelines, getting it right requires expertise. Tune in to hear their advice on how to deliver these documents with accuracy and efficiency!