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Ursula Tschorn – Project Expert for Terminologies in Health Care
I am interested in working as a terminology expert in international projects with drug coding issues in cross-functional teams as freelancer.
Xing, LinkedIn: Ursula Tschorn
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As the founder of DACON Datenbank Consulting GmbH in 1989 and of IDMP1 GmbH in 2015 I have worked in drug information and medical terminologies for many years. IDMP raised the bar significantly by requiring information sent to national authorities to be in a specific form for each country and language coded with an ISO Code. So to be able to submit data, all branches of a company should share a common (IDMP) language and vocabulary. The terminology used in unstructured regulatory documents (legal data, PDFs, SmPCs) needs to be aligned throughout the company and “translated” into IDMP controlled vocabularies.
What I like best is to work as terminology expert on such international IDMP projects on a freelance base.
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- Pharmacist
- Project Manager (IPMA level C)
- IT and Data Manager Expert
- Managing Director IDMP1 GmbH
- Member of the DIN / ISO Expert Groups
– IDMP (Identification of Medicinal Products)
– MPD (Medicinal Product Dictionary) - Member of ISO IDMP ISO/TC 215/WG 6 “E-Pharmazie und medizinische Geschäftsvorfälle”
- Working as German expert and delegate in European expert panels NA 063-07-03 AA “Terminologie”
- Member of the EMA IDMP Task Force
- Member of the IDMP External Working Group (IDEX)
- Knowledge of English => Upper intermediate
- Knowledge of French => excellent
- Proven ability to collaborate within and across teams
- Proven ability to gather, analyze, and evaluate information to make recommendations and/or decisions
- Proven ability to present technical information in a clear and concise manner consistent with the targeted audience
- Expert advice to Steering Committees and Project Teams handling Extended EudraVigilance Medicinal Product Dictionary (XEVMPD) or IDMP projects
- Review existing database structure
- Review existing data sources, data granularity and data structure
- Provide a data overview, gap analysis and platform for future decision-making
- Mapping pharmaceutical companies´ unstructured regulatory documents to the required IDMP Standard Terms
- Advice on coding Medical Dictionary for Regulatory Activities (MedDRA)