EUSWISSMED looks for partnerships and clients who are looking for pharmacovigilance and regulatory compliance support for the pharmaceutical and IVD industry. We offer • R&D including requirements for clinical studies • Regulatory affairs in EU, CH and FDA • Pharmacovigilance for clinical trials • QPPV services on an interim or project basis • R&D subsidies and financing. We search for pharmaceutical industry partners to apply for common R&D study and pharmacovigilance service financing. Our expertise is in post-market authorization products as well as planning preclinical and clinical studies and material especially for combination devices (medicinal product + applicator). We master EMA and FDA regulations and admission, including documentation in safety databases or alternatively the client's infrastructure. Our team of experience medical officers and pharmacists is ready to start projects short-term.