REGULATORY AFFAIRS / PRODUCT COMPLIANCE
Scienify helps coordinate regulatory affairs work for cosmetics and medical-device projects, connecting product teams with the expertise and partners needed for each market.
REGULATORY WORK, CONNECTED TO THE BUSINESS
Regulatory questions affect timing, documentation, claims, partners and launch sequencing. We help make those questions visible early and coordinate a clear workstream around the product and intended market.
Coordinate product-documentation, labelling, claims and market-preparation workstreams with the responsible specialists and partners.
Support regulatory-affairs workstreams for medical devices, connecting technical, quality and commercial stakeholders to a shared plan.
For cross-border projects, help brands organise communication between product owners, regulatory specialists, local partners and distributors.
A PRACTICAL WORKING MODEL
Scienify can support the coordination around a project. The specific regulatory interpretation, formal submissions, local representation and final decisions are handled by the responsible product owner and appropriately qualified professionals in the target market.
Product, intended purpose, claims, current documentation and target market.
Identify open questions, responsible experts, partner roles and dependencies.
Maintain clear communication, documentation flow and commercial alignment.
Keep launch and lifecycle decisions connected to the agreed workstream.
REGULATORY + EVIDENCE + MARKET ACCESS
REGULATORY AFFAIRS ENQUIRIES