OUR TEAM
VALOS’ statisticians
Based in Genoa
Our organization is headquartered in Genoa and stands as Italy’s leading entity in the realm of biostatistics and statistical programming services for Phase I to IV Clinical Trials, spanning drug and device development studies.
Our professional dedication is intently focused on delivering operational excellence to the pharmaceutical industry. We specialize in generating top-quality research, thereby fortifying our clients’ clinical trials and transforming them into resounding successes.
Our Key Advantages
Our strengths encompass a spectrum of attributes:
- Delivering clinical data with unparalleled accuracy.
- Consistently meeting predetermined timelines.
- Tailoring services to align with distinct budgets.
- Nurturing a customer-centric approach.
- Implementing a rigorous independent quality control process.
- Empowering our staff with ongoing, adaptable training and development to thrive in an ever-evolving landscape.
Guided by Pragmatic Mathematician
At the helm, we are led by Dr. Dmitri Petratchenko, a pragmatic mathematician and Professor at the University of Genoa, where he imparts knowledge in SAS programming. With a PHUSE membership dating back to 2007 and over two decades of experience as a Senior Statistical Programmer and Clinical SAS programmer, Dr. Petratchenko ensures the highest standards.
VALOS is home to a team of seasoned clinical research professionals, featuring statisticians with doctoral credentials and adept SAS statistical programmers. This dedicated team oversees every facet of our services, from project inception to post-trial quality assurance.
Pharmaceutical, Biotech, and Device Companies
VALOS collaborates closely with both small and mid-sized pharmaceutical and biotech enterprises.
Within the rigorously regulated pharmaceutical landscape, we take a hands-on approach to oversee the entirety of the biostatistics aspect of clinical trial processes. This expertise is also extended to some of the world’s largest pharmaceutical corporations whenever the opportunity arises.
Experience in statistical analysis modeling
Our deep-rooted expertise in statistical analysis modeling, coupled with extensive industry training in 21 CFR Part 11 and GCP, positions VALOS as a leader in meeting regulatory standards.
Furthermore, our consistent adherence to the industry benchmarks set by the Clinical Data Interchange Standards Consortium (CDISC) empowers our clients to attain the highest quality in their clinical trials, ensuring both on-time project completion and exceptional work quality.
Our Statistical Analysis Plans
Our Statistical Analysis Plans have garnered acclaim from our clients in diverse regions, spanning Europe and the United States of America.
These plans, which encompass various methodologies such as MMRM, multiple imputation, multiple testing strategies, and multiple failure time models, have been commended for their efficacy and their capacity to drive favorable outcomes.
