No, it’s not important.

It’s more than that. It’s .

Across the pharma world, the alignment to guidelines and rules set out by the regulatory authorities, and indeed the often even stricter requirements laid down by clients themselves must be not only met but exceeded in order to deliver success.

With full-service companies such as QUINTA-ANALYTICA operating under three practices, GMP, GLP, and GCP, the breadth of adherence is even greater.

This critical role, that underpins every modern pharmaceutical company, falls on the shoulders of the Quality Assurance team and who despite the challenges of the past year continued to meet their obligations and continue to deliver their high-quality services to both clients audits, and indeed the state authorities inspections in both the human and veterinary drugs areas.

As the slow return to normality starts, and the number of audits returning to the more usual 25-30 per annum, Quinta’s QA team are excited to move away from the remote audits of 2020, and back to the in-person visits whereby they can demonstrate the transparency and excellence that Quinta’s whole team deliver day in, day out.

Ready to start your next project? Quinta are here to assist.

Additional News

  • 19 December 2023

    Happy new year 2024

    As we bid farewell to 2023, it's time to express our deepest gratitude for the collaboration.

  • 4 December 2023

    Our new clinical unit in Ostrava comes to life

    It's a great pleasure to announce that after two years of hard work, the brand-new clinical unit in Ostrava with 36-beds capacity has been opened.

  • 3 October 2023

    Meet us at the heart of Pharma, CPHI 2023

    Quinta-Analytica is attending CPHI 2023 in Barcelona