Two decades of Asia-Pacific regulatory expertise — documentation, testing, audits and registration approval, so your product reaches shelf compliant and on time.
Regional regulatory complexity, managed end-to-end.
Every Asia-Pacific market has its own registration process, labelling rules and testing requirements. Our regulatory affairs and QA team manages the detail — dossier compilation, stability and analytical testing, facility audits and registration submissions — so products move to market without compliance surprises.
A structured path through regional compliance.
Compiling the technical file each target market's regulator requires.
Analytical and stability testing to confirm the product performs as specified.
Managing submission and queries with the relevant regulatory bodies.
Monitoring regulatory change and maintaining registration status.
Every batch we supply is tested at factory and independent labs according to regulatory requirements, GMP standards and any custom requirements. Test results for each batch are compiled into Certificates of Analysis and typically include Physical Testing, Assay Testing, Microbiological Testing and Heavy Metal Testing to ensure compliance against Finished Product Specifications. We also conduct pre-launch and post-launch Stability Testing, including Zone IVb, to justify product shelf life. We welcome factory audits by independent auditing companies and brand QA teams.
Tell us your product and target country — we'll map the registration pathway.