Clinical Research Organization (CRO) support by Novellas Healthcare
Trusted CRO support for Phase IV Clinical Trials in the Benelux
As a Contract Research Organization (CRO) based in Belgium and serving the whole Benelux region, Novellas Healthcare provides full service for Phase IV clinical trials.
Our expertise is trusted by both biotech startups and major pharmaceutical companies, thanks to our proven track record of delivering rigorous, high-quality work.
Recognized for our professionalism and dedication, we help ensure successful non-interventional studies, safety monitoring, and real-world evidence collection to improve patient outcomes and meet regulatory requirements.
The partner of your next Phase IV clinical trial:
Regional Expertise in the Benelux
With a deep understanding of the regulatory environments in the Benelux region, Novellas Healthcare ensures that your clinical trials are conducted smoothly and in full compliance with local and European regulations.
An experienced team with over 20 years of industry involvement
Our skilled professionals bring more than twenty years of experience in clinical research.
From recruitment until reporting, we offer expert support at every stage of your clinical trial; ensuring quality and results.
Adaptive solutions
We understand that your clinical trial is unique.
That’s why, even in this area, we offer personalized solutions that are flexible and adaptable to your project’s specific requirements, ensuring your clinical trials achieve their goals on time and within budget.
Plan a contact with us to learn more about solutions to personalize your clinical trial: contact-us.
A full service CRO... and +
You receive end-to-end patient services, including non-interventional trials, medical need programs, and patient support programs. This makes us your one-stop partner for all phases of product development.
Our services
Data management
Our team brings specialized skills in statistical ability, clinical data programming, and advanced statistical analysis, alongside CDISC-related services. This ensures that your clinical trials benefit from accurate, efficient, and fully regulatory-compliant data management.
Clinical Operations Support
Our CPMs, CRAs and CTAs provide tailor-made services and functional services according to your needs.
Regulatory Affairs
Trust a team of experts in regulatory affairs, supporting you in various tasks such as:
- CTD
- Integrated summaries for NDAs
- Briefing documents
- Clinical expert statements
- Query management.
Biostatistics
Expertise in clinical data programming, statistical analysis, CDISC related services, reporting.
Our team has years of proficiency in biostatistics in various steps of clinical studies.
Study Management
A committed clinical trial project director is assigned to your trial, to guarantee you the best operational roll-out.
Scientific Communication
A dedicated team, available to write, review and perform a list of scientific documents adapted to your clinical trial, such as:
- Protocols
- Scientific abstracts, posters and slide presentations
- Patent descriptions
- Preclinical study reports
- Scientific literature reviews
- Website content.