Workshop room 1 15:30 to 17:30
Mª Àngels San (Project Division Director)
Eduard Cayon (Audit Division Director)
From TDV, as a leading consulting company in the sector, we are pleased to share with you our extensive experience in quality digitalization and GMP compliance.
The pharmaceutical sector has been in the process of transforming support tools towards complete digitalization for years, abandoning paper and improving the efficiency and effectiveness of operational and control processes.
It is, without a doubt, one of the most important strategic challenges for companies, which involves a complete redesign of processes and a new way of working, which, if well oriented, opens up opportunities and allows companies to position themselves in an increasingly competitive environment. Digitalization makes it possible for these companies to finally measure the real costs of quality and regulatory compliance.
In the workshop we will identify, from experience, the key processes of the digital quality environment and the benefits of digitisation. In addition, we will have the opportunity to share concrete experiences that will help to visualize how to address this challenge in each company.