Follow the links below to find out more about specific services from our UK website.
TMC have extensive experience producing & maintaining submissions to all major authorities worldwide.
TMC provides full pre-clinical support covering data review, liaising with non-clinical pharmacology and toxicology units, manufacturing/quality including import and release.
Product Development Strategy & Planning, full-service support for Phases I-IV clinical trials.
TMC is a Market leader for rare populations & Orphan Products.
TMC holds Marketing Authorisations in Europe and other ex-US territories (providing regulatory maintenance, medical and scientific service, distribution, etc) on behalf of clients when required.
The TMC team probably has more Orphan Product and cell therapy experience than any other service provider. We obtain and hold Orphan designations worldwide, run clinical trials quickly, and support pre- and post-approval marketing.
Strategic, expert consultancy, across all stages of Pharma/Biotech/Device development Global Dev. Plans, KOL management, Project Management, Audits & Pre-Approval Inspections.
Global pre- & post-approval safety management, (cases, periodic reports, PSMFs), experienced QPPVs, expert medical support, using an Argus database.
Experienced Industry Physicians that support Sponsor’s PV & Medical teams. Extensive clinical trial experience, pre- & post-approval, 24-hour global Medical cover.
TMC’s team Include members of AMWA & EMWA, experts in all documents, e.g. study docs, regulatory submissions, publications, marketing materials.