About Us
We partner with Life Sciences leaders to design, build, deploy and support bespoke data-management solutions that turn regulatory complexity into competitive advantage.
Who We Are
We're a small, friendly, and agile data management consulting company based in Spain.
We choose to be self-funded with no outside capital, which means freedom and independence. You choose us and we choose you!
Our team of experts crafts bespoke solutions to data management challenges faced by Life Sciences organizations.
We offer our clients a single point of contact for fast decision‑making.
Our dedicated Founder and CTO personally guides your project to success.
Our Clients Benefit From
Fixed Cost. Fixed Timeline. No Hidden Fees.
We agree on scope, timeline, and cost upfront. You get a final deliverable with complete transparency and no surprise invoices.
Full Transparency via Our Client Dashboard
Direct access to our scheduling tool (Monday.com). Watch our work progress in real-time and know what we're working on.
Know Your Team and What They're Working On
Work directly with developers writing the software. No layers of project managers or account managers—just direct collaboration.
No Project Managers
No Project Management on your side, we self-manage. You provide requirements and feedback while we handle the rest.
Our Values
Human
All business is personal, we bring our whole selves to work.
Humble
We're not afraid to admit our ignorance and/or mistakes.
Humorous
Life's too short, we make working with us fun.
Hungry
We want to contribute to solve real problems.
We're Passionate About Life Sciences
We're a 100% remote company and we put family first. We believe the team's quality of life is crucial to the success of the company.
We Define Quality of Life As:
- • Physical and mental health comes first.
- • Work comes and goes, family is forever.
- • Live wherever you feel best.
- • Make time to do what you like.
- • Enjoy your colleagues.
- • Choose clients you like.
- • Constantly take opportunities for growth.
Published Papers
PharmaSUG 2021
This paper presents a Python-based platform that generates Synthetic CDISC Clinical Trial Data at scale. The platform programmatically generates realistic synthetic persons (SynthPerson) that have a complete synthetic Personal Health Record (SynthPHR). Each SynthPerson lives in a series of geographically-accurate synthetic cities (SynthCity). Groups of SynthPerson are then randomly enrolled in a synthetic Clinical Trial (SynthTrial). Platform users define the parameters of each synthetic clinical trial and the platform generates all CDISC SDTM domains for the desired number of subjects.
PHUSE EU Connect 2023 - Human BioGeography
Human BioGeography: predicting clinical trials outcome using a 3D human body simulation and a GIS framework
Diego Caso, TrialTwin and Rocio Matesanz, PhD Student
Due to the limited success rate in clinical trials, with less than 20% of drug candidates progressing through all phases for marketing approval, novel innovative approaches remain essential to improve these statistics. This paper proposes a novel system combining relevant databases from different Open Data sources with a Geographic Information System (GIS) that will contribute to confront this challenge. By integrating information from several biorepositories, including previous reports of drug development processes, into a 3D simulation of the human body our system aims to identify determinants restricting clinical trial success. We call this "Human BioGeography" and is based on a hierarchy of anatomy => disease => therapeutic target => drug => chemical structure. This approach provides crucial insights for drug developers, offering data on aspects that influence drug approval rates, such as potential adverse events and drug viability and metabolism. This system is expected to improve both trial design and development processes, revolutionizing the clinical trial landscape.
PHUSE EU Connect 2023 - Metadata-Driven Platform
Sergio Alegria
Increasing Business Impact of Connected Standards with a Metadata-Driven Platform
Regulatory agencies require sponsors of drugs, devices, and veterinary products to comply with specific standards and terminologies for all submissions. There are multiple Standards Organizations that develop and curate multiple data standards. Standards are available in many sources and formats, creating a complex ecosystem in the communications between Regulatory Agencies, Standards Organization, sponsors and CROs. While standards are a central piece in an organization's operations, the management of said standards is a complex task that impacts the process of bringing a new product to the market. TrialTwin's Data Standards Governor is a system that allows organizations to manage their own standards and terminologies, having a baseline of pre-loaded standards and terminologies from Standards Organizations (CDISC, LOINC, ..). The system provides organizations with tools to define connectivity between standards and terminologies to enhance metadata usability throughout the organization.
Contact Us
José C. Lacal, CTO
Phone
{Spain} +34 (674) 88 17 52
Office
Data Santander, SL
San Fernando 16, 6C
39010 Santander (Cantabria)
Spain