VALOS | Statistical solutionsfor your clinical trial

Statistical

Solutions

for your clinical trial

We Provide

Data Management

Statistical Programming

Biostatistics

WHO WE ARE

Your clinical
trial’s success

We deliver better quality and on-time completion of projects.

Our team is made of clinical research professionals, having strong education, wide experience and on-going training of the main industry information (such as 21 CFR Part 11 or GCP), market trends and industry standards such as Clinical Data Interchange Standards Consortium (CDISC).

2002

2002

founded

6+

6+

offices worldwide

500+

500+

clinical trials

80+

80+

programmers

WHY CHOOSE US

Few Reasons Why You
should Choose Us

Accuracy

Providing clinical data with utmost accuracy.

Punctuality

Always delivering services within the specified timelines.

Customer focus

Tailored services to suit specific budgets, having a customer-centric approach.

OUR SERVICES

What We Offer for You

VALOS helps you to drive your clinical trial’s success.

Data Management

DM team follows GCDMP, CDISC CDASH standard and is experienced in working with Medidata RAVE, Oracle Inform and more.

Biostatistics

Our experts work with clients to identify innovative methods to collect, analyze and present data with regulatory guidelines.

Statistical Programming

Our programmers provide clinical study reports as submission-ready deliverables to clients in a bid to make their clinical trials more effective.

Auditing

Assessing the compliance with the applicable standards, tour of site, documentation’ check archiving of documents and more.

Real-World Evidence Solutions

To support your launch preparation, reimbursement submission, pricing and Market Access strategies we can build together database analyses.

GDPR

We, in partnership with the law firm Studio Legale Castagno & Associatiprovide, qualified designed EU representative.

WE MAKE CONNECTIONS

Meet Our Leadership

The team is headed by Dr. Dmitri Petratchenko, a pragmatic mathematician who has more than 20 years of experience as Senior Statistical Programmer and Clinical SAS® programmer, PHUSE member since 2007. He stays involved throughout the project, ensuring strong science and consistent quality.

Dmitri Petratchenko

CEO

Andrea Parodi

Head of Biostatistics

Mikhaela Miliotti

Head of Business Development

We Take Care of Your Clinical Trial

Focus on Your Business

RECENT NEWS

Our Latest Insights

News

SCDM 2025 EMEA Conference. Influencing with Authority. 9-11 April 2025. Brussels, Belgium

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News

4th Ace Clinical Trials Summit, London 2-3 April 2025

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News

BioPharma Clinical Trials Nexus, Hyperion Hotel, Basel Switzerland – 13-14 March 2025

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News

EPA Congress, RAI Amsterdam, 5th – 6h March 2025

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News

ACDM , Clarion Congress Hotel,Prague 2nd – 4th March 2025

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Webinars

Webinar: Inference on weighted data

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Get a Free Consultancy

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