IZiel works in collaboration with your team to develop the complete Design History File (DHF) including requirements management, risk management, process validations and software validations using robust design controls process and quality system procedures. Thereafter, IZiel team works with their regulatory team in USA to complete the submissions (510k or PMA) and resolve queries, if any, from USFDA.
Read more@ https://iziel.com/regulatory-remediation/
We understand that taking your cosmetics to a different country or continent may seem like a daunting process at the first go.
You may not be certain about how things work and may be wondering how to navigate a foreign Regulatory landscape.
Fryers’ local experts can guide you throughout the process and make things easy for you“End-to-end” Regulatory services customized for large, small-medium, and very small businesses, with a team of local experts supporting you with the following services worldwide.Freyr provides end to end Cosmetic Regulatory Services like formulation; ingredient review, label review, claims review, safety assessment; toxicology services, dossier compilation and market entry support.