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

  • 31 May 2023

    Clinical Tips – Drug Interactions in Advanced Clinical Trial Design

    Drug interactions play a key role in the design of clinical trials. Learn how we investigate such interactions when conducting pharmacokinetic/bioequivalence studies and while offering end-to-end support throughout the process.

  • 6 April 2023

    Transdermal Patches, Films and Topicals – Putting the Skin in the Game

    Today we talk about novel drug delivery systems and in vitro testing techniques. Learn about our work with transdermal patches, orally dissolving films, topical products and Franz cell testing.

  • 23 March 2023

    A Prescription Against EU Medicine Shortages – Outsourcing Stabilities

    We highlight the reasons behind current EU drug shortages and the key role CROs and outsourced stability testing play in diversifying drug production.