Our first step is always to discuss your organization, opportunities, product portfolio, the quality and availability of data and documents and your timelines (roll-out plan). We will also highlight relevant EU and local member state regulations and how our services match with both your context and the safety and regulatory requirements. We are flexible to use the latest conference communication tools at a day and time that is convenient to you.
Important input at this stage is information on product formulation, ingredients, daily dosage, intended markets, shelf life and product claims.
Once received, we will scan your formulations for EU and specific member state regulatory compliance, review your documents and data on quality and completeness, and have one of our experts perform a high-level review to highlight any potential safety related concerns.
The Prescan will provide you insights in the possibilities, steps to take, lead-times and the needed resources to have your products EU member state market ready. Once your products are market ready and in most cases notified, you can confidently market your product.