ME-TA Information

ME-TA is a Danish biometrics CRO. We provide biostatistics and statistical programming to pharmaceutical and biotech sponsors, and we run Metawebservice, the validated platform our work is delivered on. What we do: • Biostatistics and trial design, including integrated analyses (ISS/ISE) for regulatory submissions • CDISC SDTM and ADaM datasets, define.xml and reviewer's guides • Tables, figures and listings for clinical study reports and submissions • Controlled sharing of clinical data with people outside your organisation, for DMC packages, vendor handovers and due diligence Metawebservice is where the work lives. Clinical data is stored in Europe, encrypted, with every version kept and every access recorded. You decide who can see which study, including people outside your own company, and you can take an export at any time. The platform is validated to GAMP 5 against a written requirement specification, and documented against 21 CFR Part 11 and EU Annex 11. Our quality management system is 22 policies, each version-controlled with an effective date, published at policy.me-ta.dk. ME-TA was founded by Martin Eeg and Toni Awwad, who built Metawebservice together. Martin is a statistician with more than 20 years in pharma, including work inside the statistics departments at Novo Nordisk and Novartis. Toni is a statistical programmer and CDISC specialist, with more than 20 years of experience in clinical programming, in-house at Lundbeck and Genmab, and is the company's Data Protection Officer. Agern Alle 5A, DK-2970 Hørsholm, Denmark. CVR 37265705. contact@me-ta.dk