Let’s take the opportunity to meet at the Drug Delivery to the Lungs Conference 2019 in Edinburgh and discuss future business collaboration. Our expert Eero Strandman will be available at the conference, ready to talk with you about any business queries you may have.
Medfiles offers comprehensive analytical services for chemical and microbiological analyses. Our laboratories have GMP certificates and a GMP license which covers also the manufacturing of investigational medicinal products (IMPs) for clinical trials. We perform stability studies according to the ICH/VICH guidelines and additional tailor-made studies according to the clients’ needs. Method development, validation and transfer to various analytical techniques with complete documentation according to the current regulatory guidelines are just some of our strong areas. Comprehensive quality control analytics as well as certification and batch release of drug substances, excipients and finished products by a Qualified Person, also as regards the re-analysis of pharmaceutical products for the EU market, are part of our laboratory service portfolio.
If you are interested in knowing more about our services, such as analytical method development and validation, QC analyses / batch release, stability studies or supportive analyses for product development of inhalation products, please contact the Medfiles Analytical Team. Or connect with Eero Strandman on LinkedIn or via email and book a meeting at the DDL2019 conference.
Eero Strandman
Manager, Business Development
Mobile +358 50 370 2360
Visit our website to learn more about Medfiles’ R&D and laboratory services
