Rousselot's expert services

We continuously monitor new and evolving regulations in the gelatin and collagen sector and maintain contact with regulatory bodies around the world, either directly or through associations including IPEC, GME, GMIA, SAGMA, GMAP and GROW. This ensures maximum compliance and global availability of our products.

We assist customers in navigating changing regulations specific to collagen and gelatin.

For biomedical products, we provide comprehensive support, including quality documentation, certifications, import assistance, confidential data management through Drug Master Files (Type IV excipient DMF or MAF [Device Master File] in US, excipient DMF in China), and market-specific compliance verification. Our expertise allows customers to focus on innovation while we manage the regulatory landscape, to ensure a smooth path to market approval.