OZQA COMPANY

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Practical insights on Quality Management Systems, GxP compliance, Pharmacovigilance, and ISO-based quality systems for pharmaceutical and medical device companies.

OZQA featured in Science Report: Skills shortage is a growing bottleneck in life science

OZQA is featured in Science Report highlighting how lack of competencies, not regulation, is slowing the life science industry. Learn how to

OZQA Opens for Partnerships with Life Science Consultants and Industry Experts

OZQA invites life science consultants and regulatory experts to collaborate on quality systems, pharmacovigilance and compliance projects.

Louise Søgaard Nielsen Joins OZQA as Pharmacovigilance Consultant in Europe

Louise Søgaard Nielsen joins OZQA as pharmacovigilance consultant, strengthening EU pharmacovigilance and GVP compliance support for biotech

OZQA Expands Quality System Support for Medical Device Companies

OZQA expands consulting support for medical device companies with ISO 13485 quality systems, SOP development and notified body audit prepara

OZQA Launches Webshop with Ready-to-Use Quality and Pharmacovigilance Documents for Biotech Companies

OZQA, a European quality and compliance advisory for life science companies, has launched a new online webshop offering ready-to-use SOPs, log templates and regulatory documentation designed specifically for biotech companies outsourcing clinical studies. The webshop provides practical documentation packages that help companies establish or strengthen their quality systems and pharmacovigilance processes while working with external clinical research organisations (CROs). Biot

Why OZQA Was Created: Simplifying Quality Systems in Life Science

Learn why Hasse Herlevsen founded OZQA to help biotech, pharma and MedTech companies build practical quality and compliance systems.