2017-10-06 | PPMA: Ensuring Serialization Solutions are Flexible enough for Future Growth

 

Alastair Taylor pictured with PPMA TV crew. 
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2017-09-29 | Complications of Europe's Falsified Medicines Directive

Now let’s look at some of the complications for drug manufactures when meeting the Europe's Falsified Medicines Directive (FMD), and particularly the Delegated Regulation.

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2017-09-22 | Europe’s Falsified Medicines Directive (FMD) Explained

 

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2017-09-01 | Meeting the Falsified Medicines Directive (FMD)

Companies who market prescription drugs in any part of Europe should pay close attention to the new requirements spelled out by the Falsified Medicines Directive (FMD) and Delegated Regulation (DR).  The FMD/DR spell out new and complex requirements for applying randomized unique identifiers to almost all prescription drug packages marketed in the EU by February 9, 2019.  That date is now less than 18 months away.  And it’s not just the EU Member States because other European countries have...

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2017-07-21 | EU FMD and US DSCSA Changes

As the dust settles on the recent FDA news on the DSCSA timeline, I’m sure lots of organisations are wondering what this means to the rest of the world.

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2017-03-28 | Data Sharing Required by European Hub; Pharmacies to Verify Before Dispensing

Drug manufacturers who market drugs in Europe will need to begin applying unique identifiers and an anti-tampering device to their packaging by February 9, 2019. Most companies are already aware of these well-publicized requirements of the Falsified Medicines Directive (FMD) and the E.U. Delegated Regulation (EUDR). Systech offers packaging line management and serialization solutions that will allow you to easily meet these requirements. But you might not be aware of the other big...

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