Quality & Process Validation

Applied assists and supports companies in the pharmaceutical, medical, cosmetic and food sectors by providing advice and support in the creation of qualification and validation documents, as well as useful tools for verifying, maintaining and archiving the information that is produced during the design and testing of automation systems.

Support in risk management and go-to-market

No more operational inefficiencies and project delays.

Applied offers Equipment Validation, Quality Assurance, Quality Control & GMP Compliance, and Commissioning & Qualification services to identify, evaluate, and improve processes related to product quality and compliance on an ongoing basis throughout the entire process, from manufacturing to distribution, to ensure that the product meets the required safety, compliance, and quality standards when it is placed on the market.

We help companies achieve
compliance with regulatory requirements

Ongoing, continuous support and strategic consulting, including remotely

Equipment Validation – We guarantee that your machines, plants, and equipment comply with the quality and safety standards required by the pharmaceutical industry, reducing the risks of non-compliance.

QA, QC & GMP Compliance – We provide consulting and support for the preparation of technical documentation necessary to ensure full compliance with GMP quality requirements and the resulting marketing authorization, also facilitating the certification and audit process.

Commissioning & Qualification – Seguiamo l’avanzamento dello sviluppo dei sistemi (Design Qualification) direttamente presso il fornitore. Inoltre, eseguiamo test rigorosi per assicurare la corretta installazione e il corretto funzionamento di macchine e impianti, per assicurarci che operino in modo efficiente e sicuro, garantendo la qualità del prodotto finale.

Applied supports your company during all the project stages

01
Pharmaceutical, medical or cosmetic project definition
02
URS
03
GMP Analysis
04
DQ and related specification documentation
05
Machine, plant or software realization
06
FAT/SAT
07
IQ, OQ, PQ
08
SOP, IO