Some of you may know that I’ve been working with the WHO, UNDP, FIND and others to write a handbook for local manufacturing of diagnostics in LMICs.
We now have extensive material on lateral flow manufacturing but we’re in need of additional writers and reviewers for the technical content on manufacturing molecular diagnostic kits. If you have experience of manufacturing IVDs or reagents within a quality management system (not necessarily within an LMIC!) and would have a few hours in the next two weeks to help review or to draft a short section in a collaborative document, please let me know either here or via email@example.com
Thanks so much!