Macsa ID, a leader in marking, coding and traceability solutions, together with Adents, experts in serialisation, are proud to present SERIAL FARMA, the most comprehensive global solution to comply with the new mandatory regulation on pharmaceutical serialisation.
The Falsified Medicines Directive (Directive 2011/62/EU) establishes solutions to combat counterfeit medicines. It is a key priority in the Medical and Pharmaceutical Sector as all pharmaceutical laboratories with prescription medicines must comply with the EU-FMD before the deadline of 9th February 2019.
On the 5th October we attended the ‘Are you ready for serialisation?’ conference organised by AECOC (in Madrid), where we participated in the roundtable to discuss the new regulations, inform manufacturers of the effect they will have and offer our different solutions. We were also present at the same event held in Barcelona on 18th October.