TOPRA's Regulatory Affairs Live workshop (half day) is aimed at students, recent graduates and young professionals who are starting or looking to start a career in regulatory affairs.
Invited speakers include key regulatory professionals from pharmaceutical companies (e.g. Pfizer, Astra Zeneca, GSK), regulatory consultancies, regulatory agencies (eg EMA, MHRA), regulatory recruitment companies and careers coaches.
For further details see: http://www.topra.org/TOPRA/TOPRA_Member/floating/Regulatory_Careers_Live.aspx
The Institute of Validation Technology are holding their 7th Annual Validation Week in the Hilton Hotel in Dublin this April. See the link below for more details and to download a brochure.
The European Parliament and Council has recently approved and published the Delegated Regulation (EU2016/161) in the Official Journal of the EU. The Regulation supplements the Falsified Medicines Directive (FMD) and introduces two mandatory safety features that will allow medicines to be verified and authenticated:
a unique identifier (a 2D data matrix code and human readable information) to be placed on medical products that can be scanned at fixed points along the supply chain;