European Union International Organization for Standardization (ISO) for the identification of medicinal products (IDMP) task force meeting

• Date:
  Tuesday, 13 December 2016, All day
• Location:
  European Medicines Agency, Amsterdam, the Netherlands

The European Union (EU) International Organisation for Standardization (ISO) identification of medical products (IDMP) / Substance, product, organisation and referential (SPOR) data task force meeting with representatives from the European Medicines Agency, terminology organisations, software vendors and developers of medicinal products dictionaries / databases will discuss aspects of planning, development, implementation and maintenance of the ISO IDMP standards in the EU, in line with requirements defined at international level and based on agreed EU implementation principles.

Documents

Agenda - European Union (EU) International Organisation for Standardisation (ISO) identification of medical products (IDMP) task force meeting

Draft Reference Number: EMA/746283/2016

Minutes - European Union International Organization for Standardization (ISO) for the identification of medicinal products (IDMP) task force meeting

Reference Number: EMA/871857/2016

Presentation - Heads of Medicines Agencies (HMA) update on Substance, Product, Organisation and Referential (SPOR) (Francisco Penaranda, EMA)

Presentation - Identification of medicinal products (IDMP) actions log on Substance, Product, Organisation and Referential (SPOR)

Presentation - Organisations Management Services (OMS) project report (Kepa Amutxastegi, EMA)

Presentation - Referentials Management Services (RMS) project report (Isabel Chicharo, EMA)

Presentation - Veterinary and Substance, Product, Organisation and Referential (SPOR) (Jos Olaerts, EMA)

Presentation - Substance, Product, Organisation and Referential (SPOR) communication update (Agnieszka Laka, EMA)

Presentation - Substance, Product, Organisation and Referential (SPOR) programme timelines

Presentation - Substance, Product, Organisation and Referential (SPOR) impacts on processes

Presentation - Substance and Product (S&P) project(s) and sub-group status update

Presentation - Regulatory Optimisation Group update (Joris Kampmeijer, MEB)

Presentation - Summary of substance sessions at task force and built upon at the follow up identification of medicinal products (IDMP) workshop