What we do
across industries
Select a sector to explore our full range of regulatory, scientific and quality services.
Cosmetics
Full regulatory lifecycle support for cosmetic products across EU, US, GCC and Asian markets. We handle safety assessments, CPNP notifications, labelling compliance and GMP documentation so your product reaches consumers safely and legally.
Explore Cosmetics services →Food Supplements
Regulatory strategy for nutraceuticals and food supplements — from novel food authorisations and health claim substantiation to labelling and maximum permitted levels across EU and international frameworks.
Explore Food Supplements services →Medical Devices
End-to-end MDR compliance pathways for Class I–III medical devices. We prepare technical documentation, clinical evaluation reports, post-market surveillance plans and manage Notified Body interactions on your behalf.
Explore Medical Devices services →Pharmaceutical
Strategic regulatory affairs for medicinal products throughout the development lifecycle — from IND/CTA preparation and CTD dossier assembly to EMA/FDA submission management and pharmacovigilance system setup.
Explore Pharmaceutical services →Core capabilities that
span every engagement
- Regulatory strategy & intelligence
- Quality system design & compliance support
- Market entry & import/export compliance
- Post-market surveillance & CAPA