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Pharmaclean® is the AM Instruments® production for cleanroom contamination control

Products specifically designed to meet the needs of our customers in terms of effectiveness, safety and compliance with regulatory requirements.

Pharmaclean is the result of the experience we gained in 30 years of activity: thanks to this know-how we were able to create products that fully adhere to the increasingly stringent quality and safety requirements that the life science sector requires.

Pharmaclean® creates personalised products and solutions according to customer needs

Pharmaclean meets the special needs of the life science sector, producing customized protection, packaging and sterilization systems. Each customer request is discussed with the support of our QA, which defines the operational flows and every verification and release test needed in order to offer a GMP compliant service in accordance with the specific requests of the customers themselves.

Samples and quotations can be requested using the interactive form, which allows the customer to provide all usefull information so that Pharmaclean operators can offer a quick and effective answer regarding the production of the sample and / or the listing of the product.

GMP Consistent AM Instruments

Sterilisation & Packaging Solutions

Production of pouches and rolls in Tyvek® – PET/PP poly-bonded material for sterilisation operations. Biodecontamination process of raw materials from viable and non-viable particles with the unique Safe4Clean® system. Standard and customised solutions available.

Covers & Sterility Protection Solutions

Manufactured in Grade A/B cleanrooms, Tyvek® cover and packaging systems for sterilisation and protection from dust, particles and micro-organisms offer total safety and resistance, are customisable and easy to use. Incorruptible after autoclaving and not subject to breakage.

Pharmaclean® services

In accordance with the GMPs, Pharmaclean® offers a repackaging service for pharmaceutical applications and a DPTE-BetaBag® repackaging service for isolator and RABS applications.

GMP Consistent AM Instruments

Quality control

Every stage of the process, from the acceptance of raw materials to the release of the product, is strictly controlled and every work space is subject to environmental and microbiological monitoring.


Each lot is delivered along with the environmental and microbiological monitoring report, the certificate of conformity and, if accomplished, the certificate of irradiation.

On-site audit

During audits, our customer can verify the compliance with the increasingly demanding quality and security requirements related to the productions areas and processes.

You can schedule an audit by sending a request to our quality department at