Welcome to the Season 5 of Freyr Regulatory Radio Consumer! We're delighted to present a consumer Regulatory podcast series dedicated to MoCRA regulations. This series introduces standardized regulations covering facility registration, product listing, safety substantiation, and adverse event reporting.
At Freyr, our goal is to simplify the intricate MoCRA Regulatory landscape through candid and direct conversations with industry experts. We strive to make these regulations more accessible and comprehensible to all stakeholders.
This season of the Freyr podcast serves as your ultimate guide, providing a clear path to understanding through expert-led discussions. Tune in and empower yourself with essential knowledge for navigating the Regulatory realm with confidence.
Understanding MoCRA's Facility Registration requirements is crucial for cosmetic manufacturers. It ensures transparency and product safety, paving the way for smooth operations in the US market. Compliance with MoCRA's facility registration requirements fosters trust and builds a strong foundation for your cosmetic brand's success in the US.
This episode untangles the role of the Responsible Person (RP) and the US Agent. We'll break down their key differences and responsibilities, ensuring you stay compliant and navigate the market smoothly. Whether you're a manufacturer, distributor, or simply curious about the industry, this episode is your essential guide to understanding MoCRA's key players. Tune in and gain clarity on MoCRA's RP and US Agent.
In today's episode, we're embarking on a deep dive into MoCRA's product listing requirements. We'll unravel what this entails, who exactly needs to adhere to it, and the crucial information that must be included. Whether you're a seasoned industry professional or just stepping into the Regulatory arena, this episode is a must-listen for anyone seeking clarity on MoCRA's product listing mandates.
MoCRA raises the bar for cosmetic safety and demonstrating "adequate substantiation" is key. But what exactly does that mean? This episode unlocks the secrets of MoCRA safety substantiation, guiding you through the process with expert insights. It also empowers you to understand and implement MoCRA safety requirements and MoCRA safety substantiation.
MoCRA brings significant changes to the way adverse events associated with cosmetic products are reported in the US. This episode delves into the nitty-gritty of MoCRA's adverse event reporting requirements, helping you understand your responsibilities and ensuring you stay compliant.
General Manager
Vishwajeet has led projects on transitioning large portfolios to EU Cosmetic regulatory compliance when this regulation was enforced in 2013. He is regularly involved in voluntary compliance audits for major cosmetic / FMCG brands primarily in case of mergers and acquisitions. His unique process optimisation & and scale-up approach have helped clients deal with huge work volumes efficiently with confidence."
