ISO 17025 accreditation

The AAT laboratory operates in compliance with the requirements of the UNI CEI EN ISO / IEC 17025: 2018 standard "General requirements for the competence of the testing and calibration laboratories".

As far as managerial and technical requirement, AAT Laboratory operates in compliance with Norm UNI CEI EN ISO/IEC 17025:2018 "General requirements for the competence of testing and calibration laboratories " and it is in possession of the Accreditation number 1357 emitted from ACCREDIA the 22/05/2013. Accreditation is made by verifying technical competence of the Laboratory about accredited methods; the accredited method lists are downloadable from ACCREDIA web site www. accredia.it

This brand is a guarantee of technical competence in the analyzes within a complete Quality System which invests every activity of the company. Extra security for our customers, who receive reliable data complying with international regulatory requirements.

Self-control register

The Laboratory is included in the Regional List of Laboratories that carry out analyzes in the context of the self-control procedures of the food industries of Emilia Romagna Region, Regional Council, General Directorate for Health and Social Policies, Veterinary Service and Food Hygiene.

The registration number is: 008 / PC / 005 of 17 October 2012.
The list is updated every 6 months and can be consulted on the website: http://www.alimenti-salute.it.

Innovative SME register

AAT Srl is an innovative SME, registered in the national register
Innovative SMEs is a category of companies with special requirements of high investment in research and development, by a work team with post-graduate training level (research doctorate) and able to provide services with a high content of technological innovation.

50% of the expenditure that our customers incur for R&D projects commissioned by AAT can be recovered as a tax credit. Based on the indications of the MISE (www.mise.gov.it), the tax credit is equal to 50% on incremental expenses in Research and Development, recognized up to a maximum of € 20 million / year per beneficiary.

Authorization of phase clinical studies I

AAT srl is activating the procedures to enter the list of laboratories authorized by AIFA to perform analyzes on samples deriving from drug studies, as defined in the AIFA 809/2015 and 415/2016 standards (www.aifa.gov.it).

Already registered in the list of laboratories authorized for this type of analysis according to Ministerial Decree March 19, 1998, our Laboratory decided to update this path to provide customers of the pharma world with this further guarantee for reliable and qualified results.