<img alt="" src="https://secure.52enterprisingdetails.com/787780.png" style="display:none;">
Skip to content
menu-icon-lq
close-icon-lq
Contact Us

Clinical Trials Therapeutic Areas

We have proven our capabilities even in very challenging pharma trials, including rescue projects, on many different therapeutic areas. 

Contact Us

We offer services in clinical trials management, clinical operations,  regulatory affairs, site management and vendor management. To date, we have worked with 20+ therapeutic areas, including 

  • Oncology
  • Neurology
  • Infectious diseases
  • Cardiology
  • Neonatology
  • Immunology
  • Urology
  • Nephrology
  • Pulmonology
  • Gynecology
  • Ophtalmology
  • Allergology
  • Dermatology
  • Gastroenterology
  • Surgery
  • Diabetes
  • Respiratory diseases
  • Rare disease
  • Metabolic disorders
  • Pediatric studies 
Maciej Nowotarski

Contact us for more information

user
Maciej Nowotarski
Clinical Operations Manager
contact-email
maciej.nowotarski@aurevia.com

Leave a contact request

Related Services

Latest news

Show all >>
Notice about a change in some of our email addresses
News
21/11/25 13:53

Notice about a change in some of our email addresses

As part of the upcoming company split on 1 January 2026, some of our email domains will change to @labquality.com starting 3 December 2025.
Read more
How do you shape regulatory complexity into strategic clarity?
News
Medical devices
18/11/25 12:35

How do you shape regulatory complexity into strategic clarity?

As AI continues to reshape healthcare, clear guidance on health data use is more critical than ever. Building on the success of the AI Act e-tool and the Data Act e-tool, the Finnish-Danish joint action has released an invaluable e-tool that sheds light on the European Health Data Space (EHDS) regulation.
Read more
Fast track for mononational clinical trial applications in Sweden
Article
News
17/11/25 13:17

Fast track for mononational clinical trial applications in Sweden

Starting September 1, 2025, the Swedish Medical Products Agency (Läkemedelsverket) introduced a fast-track process for evaluating mononational clinical trial applications for medicinal products in CTIS.
Read more
Upcoming webinar: what IVDR Article 5(5) means for your lab
News
Medical devices
17/11/25 13:00

Upcoming webinar: what IVDR Article 5(5) means for your lab

Whether your lab is already working under IVDR and Article 5(5), evaluating tests, or preparing for transition, this free online webinar will offer practical guidance to help your lab stay compliant.
Read more
IVDR reality check: are we moving fast enough?
Article
News
Medical devices
30/10/25 09:52

IVDR reality check: are we moving fast enough?

As of February 2025, approximately 1,500 IVDR certificates have been issued. That’s progress — but is it enough? With an estimated 18,700 devices still requiring certification before the end of 2029, the current pace raises serious concerns.
Read more

Subscribe to our newsletter

Subscribe to hear the latest news in the industry and keep track of what's happening behind the scenes.