TrialTrack was built by a clinical QA professional who spent years running the processes it now supports, together with two software founders who have run SaaS products together for nearly two decades.
TrialTrack is built and operated by Mayet, a software company specialising in the pharmaceutical and biotech industry.
Mayet built TrialTrack for clinical trial teams who need structured project management that supports GxP compliance without enterprise complexity.
Tom Lazenby spent his career inside the clinical trial oversight system: monitor, QA manager, QA programme lead.
At every organisation he joined, he found himself building or rebuilding systems, but when it came to clinical project management none of the tools on the market were built for how trials are run.
He partnered with Neyts Zupan and Dejan Murko, software entrepreneurs who have built and run SaaS products together since 2007, to make it real.
Together they founded Mayet in 2023.
Clinical trials quality assurance professional turned software founder. Over a decade managing quality oversight, audit programmes and regulatory inspections at GSK, UCL Clinical Trials Unit, and Imperial College London.
Single point of accountability for quality oversight across fifty-plus studies at GSK. Every workflow in TrialTrack reflects how clinical teams manage trials, because Tom has done the work.
Software engineer and technical leader with over twenty years of professional development experience. Co-founded Niteo, a remote-first SaaS company he still runs with Dejan.
Co-founded Pareto Security, a device compliance tool. International conference speaker on Python, web development and engineering productivity.
When clients ask how TrialTrack handles encryption, access control or disaster recovery, the answers come from a CTO who has built a security product.
Product leader and SaaS entrepreneur. Business partner of Neyts since 2007, through Niteo, Pareto Security and now Mayet.
Has led products that together served over 10,000 customers; several were sold in successful exits.
His role at Mayet: turn domain expertise and client feedback into a product that is simple to use and stays that way as it grows.
Mayet's advisory board brings over 120 years of combined experience in pharmaceutical and clinical research.
Former CEO and CCO with over 30 years in pharma, biotech, and CRO environments.
Executive VP Global Quality with over 30 years in clinical research.
Clinical Research Training Consultant with over 30 years in clinical trials.
Pharmaceutical Quality Consultant and former VP R&D Quality at GSK with over 30 years in medicines development.
Mayet partners with DQA, an independent quality assurance consultancy specialising in healthcare, biotech and medical devices. DQA provides compliance and validation support to Mayet and its clients, so regulatory requirements are addressed from the earliest stages of product development.
Free for up to 3 users, with no credit card and no sales call. You can be up and running in under an hour.
Begin on the Free plan with up to 3 users, all core features and no credit card required. Upgrade anytime.
