“There is only one way to explain a technology, validate it, test it and protect people from the consequences of process errors: enter into it and learn every detail of the machine and the reasons behind it”.
This is the philosophy of SPAIQ S.r.l. (hereinafter also referred to as SPAIQ): to provide useful tools for the verification, dissemination, maintenance and archiving of information that is produced during the design and testing of automation systems.
SPAIQ has been active for over 20 years in:
Its mission is to protect the health of the end user. An in-depth understanding of processes, risks and thorough testing ensures real protection of human and animal health.
Therefore, authorization for the production and packaging of drugs is only granted to pharmaceutical companies when they demonstrate that their processes comply with GMP (Good Manufacturing Practices) procedures.
This can only be achieved through accurate and precise validation, rigorously documented at all stages.
SPAIQ accompanies pharmaceutical and packaging companies in the validation of machines, carefully assessing risks and preparing the necessary documentation.
Validation is a very delicate process, concerning anything that may pose a danger to the person or animal that will use the drug once it is placed on the market or in the healthcare system. Validation of machines follows their life cycle.
In the contractual phase, the user (the pharmaceutical company) prepares the URS (User Requirement Specification) document in which it lists its requirements in terms of quality, production, safety and maintenance. Whereas the machine manufacturer must specify how he intends to meet the user’s requirements.
All parts of the system that affect quality and product safety must be explained in detail in the Validation. Careful assessment must be made of the risks that are expected to remain in spite of established actions or deliberately accepted for any possible pharmaceutical defect.
In this respect, SPAIQ also supports the customer in the selection and construction of the most suitable validation strategy. It therefore provides high-level consultancy using a compendium of experience acquired over more than 20 years of established methodologies in the field of risk analysis.
SPAIQ also carries out the testing and qualification of machines by qualified and continuously trained personnel.
To implement such sensitive services, SPAIQ relies on certain guiding values that define the identity of its corporate culture:
The company knows that improving processes (and the quality management system) is what enables it to create value for customers, end users and people.
SPAIQ is based in Villanova di Castenaso, in the centre of Italy’s Packaging Valley.
Fabio Giovanni Farneti
SPAIQ CEO