Hello, I'm Mat Parowicz, your guide through the rugged terrain of Regulatory Affairs and Study Start-Up, where regulatory excellence truly rocks! With over 20 years of navigating the pharmaceutical and clinical research industry, I am your dedicated consultant and trainer, embodying the solidity and reliability that rocks symbolize.

In this dynamic world of clinical trials, I stand firm as the bedrock of expertise, specializing in EU Clinical Trial Regulation and the robust implementation of the Clinical Trial Information System (CTIS). My journey has been a rock-solid dedication to quality, reliability, and an intricate understanding of regulatory requirements.

Picture me as the steady anchor, leveraging my extensive experience to be your trusted partner in strategically planning and executing clinical studies. Over two decades in the business have equipped me to face even the most intricate regulatory challenges, offering stability both in the start-up phase and throughout the lifecycle of clinical trials.

The introduction of the Clinical Trial Regulation EU536/2014 and the integration of the Clinical Trial Information System (CTIS) haven't just been developments in my career—they've been milestones of enrichment and satisfaction. It's a journey where I've not only learned but also embraced the role of a teacher, paving the way for a new era in performing clinical trials submissions in the EU.

On this page, explore the rock-solid insights into my services and unearth valuable resources as we navigate the regulatory landscape together. At regulatory.rocks, I don't just offer services; I offer a partnership as sturdy as a rock, ensuring your clinical trials stand firm against the trials of regulatory compliance.