We from Avanti Europe understand ourselves as holistic consultants and we are not afraid of “hands-on” support.
Our services cover the entire product lifecycle and span from brainstorming for ideas to design and development into market surveillance of highly regulated products and services. We are medical device, combination products, in-vitro diagnostics, pharmaceuticals, generics/biosimilars, homeopathy and cosmetics regulation savvy consultants enabling the possibility for a global development and registration of products and services.
We hold decade-long and detailed knowledge in international standards and regulations, such as ISO 13485, ISO 14971, ISO 10993, IEC 62366, IEC 62304, IEC 82304, MDR 2017/745, IVDR 2017/746, 21 CFR 820, 21 CFR 4, 21 CFR 201/211, MPD 2001/83/EC, ICH Q 1-12 and others.
Contact us with no strings attached for a chat on how we can support your business.