EU/UK Qualified Person (QP) Services and MIA license
Products
Information
Conducting clinical trials or launching products for commercialization in Europe can be a challenge. There are many complexities that can impede your efficiency to these markets, such as establishing a legal entity with a Qualified Person (QP) in the region, Brexit, and passing inspections to secure licenses. Whether you still need a license, or already have your MIA license in place, ProPharma can support you with strategic advice. Partnering with ProPharma and benefitting from our established MIA license will eliminate the need for you to navigate all the unique requirements across the European market. We support your swift and compliant market access by ensuring a licensed QP in the geographic area of choice and guarantying a compliant QMS is in place. We have the local expertise across Europe to help you with all the GMP/GDP tasks to make it happen.
Main Categories
Contract Services - Analytical & Lab Services
All Categories
AuditClinical Trials Phase I to IVConsulting ServicesContract Services - Analytical & Lab ServicesLogistics and DistributionProject Management
Distribution areas
OceaniaNorth America (USA, Canada)AfricaMiddle East Region (e.g. UAE)Central America (e.g. Mexico)East Asia (e.g. China, Japan, Korea)Europe - EU countriesEurope - non EU (e.g. UK, Russia, ex-CIS countries)South America (e.g. Brazil, Colombia)South Asia (e.g. India, Pakistan, Sri Lanka)
