The European Commission has published a summary report of the stakeholder event held on 20th september 2017 in Brussels.
The European Commission has published the guidelines on good manufacturing practice specific to ATMP. Other documents developing GMP requirements for medicinal products which are contained in Volume 4 are no longer applicable to ATMPs, unless specific reference thereto is made in these guidelines.
During this annual recurring symposium, attention is paid to the quality and safety of donated tissues and cells and to current developments in the field of transplantation and donation of human body materials. Due to the jubilee year, the symposium has a more international character and, in particular, invites TRIP to invite Belgian colleagues to attend the meeting. The sympos... read more
The electronic version of this Guide can be downloaded online for free at the EDQM Freepub website (https://register.edqm.eu/freepub). Paper copies will soon be available for purchase at the EDQM Store (http://store.edqm.eu/).
This Guide collates the most up to date information to provide transplant profe... read more