Our mission is to support our clients in safeguarding patients health and improving their lives in a smart, innovative and cost-efficient manner 

We promise you impeccable quality, unique attention to every detail and tailored solutions created specifically for your clinical research. We use our industry experience and know-how to constantly perfect our processes and ensure that we deliver the leanest and most cost-effective solutions.

How can we help you?

Quality Assurance

Enjoy our advanced personalised solutions for Quality and Compliance in all GxP areas and our support in designing the most effective system to meet regulatory requirements, reach your goals and improve your processes

Pharmacovigilance

Get access to a complete portfolio of pharmacovigilance services provided by our team that boasts more than 25 years of experience

Regulatory Support

Benefit from our support through all stages of drug development – from putting together a regulatory strategy document to determining your pathway forward

Our Customers About Us

“Brilliant collaboration is helping our clinical Oncology Trial Unit at Niguarda Cancer Center to achieve high quality standards in clinical trials.”

Department of Hematology and Oncology, Niguarda Cancer Center

“The seQure team ensures timely delivery of its project and is always available to accomodate our needs.”

Quality and Safety Management, Fondazione Policlinico Universitario Agostino Gemelli IRCCS

“seQure is a valuable partner in our quality related activities. The Team fully matches Customer’s needs, with expertise, proficiency and flexibility.”

Regulatory Affairs Manager, Clin Ops Coordinator, ReiThera

Contact us to learn about our expert QA, Pharmacovigilance and Regulatory services

Blog

Medical Device Regulation: what is it about? The EU’s Medical Device Regulation (MDR) is a…

On the 4th of November, we conducted the webinar “PSUR under the Medical Device Regulation:…

Regulation (EU) 2017/745 also known as the MDR, applicable since May 26th 2021, introduced a…

From on-site audits to remote audits The global spread of COVID-19 amongst other challenges has…

On the 27th of April, we conducted the webinar “Practical Advice for Your Next Remote…

In seQure, our vision is to build a world where all patients receive safe medicine…

This is the new blog in our ‘Career Insights’ series and we spoke to Andrea…

In this blog of the ‘Career Insights’ series we talk to Alessandra Marchese, Drug Safety…

News

Dear all, Hopefully you have read the recent press release published on the website of…

Verona, Italy (24 November 2020) – In anticipation of the second wave of COVID-19 pandemic…

Verona, Italy (23 October 2020) – seQure, an expert provider of Pharmacovigilance and Quality Assurance…

CROS NT, seQure and Arithmos have become a corporate partner and members of the women’s…

Events

Preparation of the Periodic Safety Update Report (PSUR) is one of the new requirements introduced…

We are excited to announce that Antonella Ursini, seQure’s Managing Director, will be speaking at…

Crucial for safeguarding the health of the patients and safe use of the drug, case…

What are the major pitfalls of GVP remote auditing and how should you address them?…

Risk management in pharmacovigilance is vital for the safe use of medicines and safeguarding the…

”To err is human.. but to persist is diabolical”. Indeed, human error is a long…