The cleanroom trade show on 23–24 October in Frankfurt will showcase the latest trends on access control, monitoring and the traceability of products
Source: Messe Frankfurt/Sandra Gätke
Access control, monitoring and the traceability of products include rules governing personal access and the items taken into cleanrooms as well as the prevention of counterfeit products.
A key principle underlies all such efforts: tracking. Current possibilities in this field will be on display for visitors to Cleanzone, the cleanroom trade show that takes place on 23–24 October 2018 in Frankfurt am Main.
Cleanrooms are classified according to the threshold values for particulate and microbiological contamination, yet the interfaces between cleanrooms and the ‘impure’ areas surrounding them, as well as between various cleanroom zones, are especially sensitive.
This is where airlocks have an important role to play. It must be possible to strictly define those who enter and exit here, and this process must be traceable.
There are various ways in which to control access, with examples including decentralised systems with control elements located directly on the doors, and central systems in which the doors are equipped with simple operating terminals.
These can take the form of touch displays or even RFID systems incorporating touch-free employee identification. In the latter case, it is particularly easy to modify individual access authorisations or implement specific restrictions.
For example only a certain number of people can be working in Zone X simultaneously, and these people must comprise defined and practised teams.
One of the challenges here involves the ability to trace which employee took a particular implement into and/or out of the cleanroom (e.g. shoes, overalls, caps, mops, wiping cloths).
Currently, one of the basic measures being used for this purpose involves ensuring that each employee is only provided with precisely what they require each day. Once work has finished, the items of clothing and equipment are then placed in specific compartments or cupboards, from where they are picked up for cleaning and/or decontamination.
This can be done by the cleanroom operator themselves, or they can utilise an external service provider. Unless there are additional controls, experience has shown that residual risks remain – such as those posed by items accidentally brought into the cleanroom, and objects left there unintentionally.
Implementation of an inventory management system designed especially for cleanrooms can help here. A basic version might involve employees recording mops, wiping cloths etc. when they enter/exit, with everything being entered in lists. This helps employees monitor their own actions.
To help eliminate any remaining risks (eg carelessness), the cupboard system can be supplemented in more complex systems with incorruptible robotics. Here, a gripper with a suction cup provides each individual employee with the items they require. For facilities in the highest security category, these processes are recorded digitally (eg in the cloud).
According to Benedikt Fischer, CTO of Dittel Cleanroom Engineering:
From a technology standpoint, these solutions are ready to be used. In fact, cleanroom utensils with integrated chips can even be tracked in detail throughout the cleanroom, and camera systems make it possible to create movement profiles for employees.
He continued: "However, there are certainly two sides to the use of such measures. On the one hand, tracking makes it possible to improve the efficiency of cleaning procedures, yet this gives rise to ethical questions regarding just how far employee monitoring should be taken, questions that must be answered. Whereas these ethical matters are already being addressed in Germany, in some other parts of the world, the focus is solely on maximising the utility of the available data.”
Tracking also means being able to trace products and avoid counterfeits – as set out in the Falsified Medicines Directive. This directive is of particular importance right now, as it must be implemented by 9 February 2019.
Basically, under the terms of this directive, the pharmaceuticals manufacturers can assign their products unique identification codes and record these in a central data hub. This gives wholesalers, pharmacies and hospitals the ability to perform a check when distributing/administering these medications: is the pharmaceutical recorded as an original preparation, or is it possible that it is a counterfeit?
A scan reveals the answer in milliseconds, allowing counterfeits to be immediately removed from stocks available for sale or use. Furthermore, special security measures integrated in the packaging make it possible to distinguish between originals and counterfeits.
Dr Heinrich Prinz from PDM-Consulting in Groß-Zimmern said: “One good method, for example, involves using a combination of two adhesives, a hot adhesive and a cold adhesive, to seal the packaging. If the secondary packaging has been opened, this ensures that this is immediately evident and makes it clear that counterfeiters may be involved.”
Such measures can also be implemented in the field of logistics, but it is important to remember that products without secondary packaging must have primary packaging that is counterfeit-proof – such as when filling directly in the cleanroom.
Furthermore, the goal of seamless tracking means that cleanroom suitable packaging and printable packaging are both becoming increasingly important.
This not only impacts primary packaging for pharmaceuticals, but also applications involving chemicals and implants.