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Air comprimé dans l'industrie pharmaceutique

Au cours de la fabrication de médicaments, les règles d'hygiène les plus draconiennes doivent être observées pour les conditions de production, en particulier dans les salles blanches. Pour cette raison, il est important que la production ait lieu dans un environnement exempt de tout germe, toute particule, toute bactérie et toute huile contaminante. Par conséquent, des exigences rigoureuses sont également applicables pour l'air comprimé, car dans le processus de production de l'industrie pharmaceutique, il entre fréquemment en contact direct avec le produit lui-même. En fonction de son utilisation, l'air comprimé doit p. ex. être stérile ou exempt d'huile. Afin de satisfaire aux obligations de fournir des preuves, p. ex. vis-à-vis d'auditeurs, une surveillance continue (24 heures / 24 et 7 jours / 7) est impérative dans le cas d'un air comprimé entrant en contact avec le produit.

Il existe différentes réglementations, telles que les BPF, la réglementation de la FDA et la pharmacopée européenne (Pharmacopoeia), toutefois celles-ci ne définissent aucune classe de qualité pour des applications individuelles. Une exception est constituée par l'air comprimé utilisé comme air respirable, vous en apprendrez davantage à ce sujet dans nos Informations Techniques médicales.

Ainsi, chaque entreprise pharmaceutique doit définir elle-même la qualité d'air comprimé requise pour son processus de production, conformément à la norme DIN ISO 8573-1. Nous vous assistons volontiers lors de la définition de la classe de qualité ainsi que lors de l'élaboration de votre solution de traitement de l'air comprimé afin de maintenir la classe d'air comprimé voulue à un niveau constant et contribuer ainsi à la sécurité des vos processus.

Applications dans l'industrie pharmaceutique

pharmaseutic application of compressed air

Tableting process

Compressed air is required for the tablet manufacturing process and this compressed air often also comes into direct contact with the product. This direct product contact occurs after the tablet press where compressed air is utilised to remove dust particles or faulty products are sorted out. Oil-free and dry air is important here otherwise, for example, the pressed tablets could swell up. Compressed air can also be used for applying lubricants onto the tablet press so that the tablets can be ejected easier.

Compressed air is already utilised at the initial stages for mixing the powder mixture and/or the production of the granules for the tablet press. The stages after the presses, the so-called coating, i.e. the coating and/or the encapsulation also utilise compressed air. A common method is the fluidised bed process whereby an air flow ensures that the tablets hover and are constantly in motion. They are sprayed, evenly moistened and dried by utilising spray nozzles. Here and in further processes, the compressed air serves as atomising air and is considered a process aid, which means accordingly high requirements are made on its purity.

Typical problems in the manufacture of tablets – in addition to the health risks for the consumer – are blistering, cracks or breaks in tablets or colour variations. Moist and oil-contaminated compressed air can be one reason for this.

Clean air room

Cleaning and drying

It is not only the machines that need cleaning; the vials, ampoules and bottles into which the medicinal product is filled also have to be especially clean. The CIP cleaning process (Clean In Place) has been established for cleaning of plants, systems and containers. Compressed air is utilised here for drying. Dry ice blasting is an addition method for cleaning. The dry ice impacts on the surface to be cleaned and loosens deposits. The loosened deposits are then blown off with compressed air.

The filter in the fluidised bed plants must be cleaned during production. This can be executed via a filter blow-out system. Material residues will therefore be routed back into the process with compressed air. There is also a direct product contact here whereby high requirements for the quality of the compressed air must be achieved.

Another application is the cleaning of vials, bottles and ampoules: In this case, the compressed air is also used for drying the vessels and removing any final particles. This often takes place in the clean room.

sterile liquids

Pneumatic conveying

Compressed air is often also utilised in the pharmaceutical industry for transporting integral elements for the production process e.g. bulk solids, liquids, powders and granules. Pneumatic conveying can be executed via compressed air or under vacuum.

When conveying takes place under pressure, the compressed air is generated and routed to a mixing head. There, it picks up the powder and conveys this to the required location. During this type of pneumatic conveying, the substances transported come into direct contact with the compressed air. This method is used for emptying silo vehicles and for distributing substances in production.

The finished products, such as tablets and capsules, are also transported back and forth between the individual processing units with compressed air. Transporting with compressed air prevents damage to the medicinal products, but a consistent quality of the compressed air is therefore required. In accordance with DIN ISO 8573-1, the German VDMA recommends a compressed air quality of sterile 1: 3: 1 for transporting raw materials and finished products.

blister packaging

Medicinal product packaging

Compressed air is used on packaging plants and systems e.g. for transporting products and packaging or for packing the product and for sealing the packaging. A controlled atmosphere will be created around the product with highly hygroscopic (water attracting) products, such as e.g. pharmaceuticals. Very dry compressed air must be present (inflating bags etc.), especially at packing positions when packaging pharmaceuticals.

There is often centralised compressed air processing, therefore the compressed air must be transported to the application location. It is possible that the compressed air is supplemented with water again on this route. Hygroscopic substances react with the moisture from the ambient air. In order to ensure the product quality, contact of the humidity with the product must be prevented. For this reason, an additional compressed-air drying is required directly on the packaging machine.

If active ingredients are filled in ampoules and vials and then sealed, a sterile environment is even required.


Regulating valve and cylinder

Compressed air is utilised as the control air in the pharmaceutical industry for regulating production plants and systems e.g. via a regulating valve and cylinder. Lower requirements are normally valid for the control air as it does not come into direct contact with the product. There are however exceptions: The control air is subjected to special requirements in clean rooms. This also applies if the control air could affect the process.

When the compressed air does not comply with requirements, then malfunctions of pneumatic tools and machines can occur, lead to corrosion in pipework, cylinders and other components as well as freezing in exposed services during cold weather. This creates a threat of increased downtimes as well as maintenance costs for pneumatic machines, tools and control systems. The correct compressed air processing and treatment as well as periodic monitoring and maintenance is therefore essential.

Clean room
Clean air room

Clean room

The production of medicinal products takes place partly in clean rooms, and some of the production steps there require compressed air. Compressed air can be used in all clean room classes. It can occur as an energy carrier in motors and pumps, for example. In these cases, the compressed air used does not come into contact with the product, but it must comply with the quality of the ambient air into which it is released. In other words: the compressed air should correspond at least to the air quality of the respective clean room class into which it is released. The requirements are worded in quite concrete terms in the “FDA Guidances for Industry: Sterile Drug Products Produced by Aseptic Processing — Current Good Manufacturing Practice”.

In the case of clean room applications, compressed air is used for drying the washed primary vessels, before filling with the product as well as for filling liquids in accordance with the blow-fill-seal method. It is important that no germs and particles are contained in the compressed air.


Applications Industrielles


Sans huile et sans germe pour les médicaments

Dans l'industrie pharmaceutique, un air comprimé exempt d'huile et de germe est particulièrement important. Pour ce faire, Nycomed utilise un filtre d'air comprimé CLEARPOINT et un BEKOKAT. Les emballages sont nettoyés avec de l'air comprimé en tant qu'air de processus et les vannes sont commandées avec de l'air comprimé en tant qu'air de commande.


METPOINT OCV chez Pfizer

Dans l'industrie pharmaceutique, la qualité de l'air comprimé joue un rôle déterminant. Les impuretés ou contaminations d'huile des produits pharmaceutiques par l'air comprimé peuvent avoir rapidement des conséquences fatales. Afin d'améliorer la sécurité des processus de la production, le site de production Pfizer à Fribourg a mis en place un contrôle permanent de la qualité de l'air comprimé, par la surveillance de l'huile résiduelle avec un METPOINT OCV de BEKO TECHNOLOGIES.