EU Guide Aims To Help Manufacturers Avoid Setting Off 'False Alarms' Under FMD
Group Concerned About Low Rate Of EMVS Adoption
To reduce false alarms of counterfeits, EU tells drugmakers no lowercase, hyphens, question marks or certain letters in serial and batch numbers.
You may also be interested in...
Russia’s new drug traceability system won’t now be implemented until July, but companies that are ready and able are being encouraged to put the system through its paces in order to flush out any glitches.
An EU guide sheds some light on what inspectors will be looking for in audits to ensure that manufacturers have the safety features required to comply with the EU's Falsified Medicines Directive.
Europe’s ambitious new system for verifying the authenticity of prescription medicines circulating on the market is about to come into operation.