Pharm Tech Agenda 2022.09.14: Difference between revisions

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== 16:00- 17:30 Supply ==
== 16:00- 17:30 Supply ==
== 18:00 Adjourn ==
Agenda woensdag
- Supply
- Supply
To do’s on supply:
To do’s on supply:
Line 58: Line 52:
https://build.fhir.org/ig/IHE/pharm-supply/  
https://build.fhir.org/ig/IHE/pharm-supply/  
White paper: https://www.ihe.net/uploadedFiles/Documents/Pharmacy/IHE_Pharmacy_WP_Supply.pdf     
White paper: https://www.ihe.net/uploadedFiles/Documents/Pharmacy/IHE_Pharmacy_WP_Supply.pdf     
== 18:00 Adjourn ==
Agenda woensdag




- Adverse events
- Adverse events
There is two level of adverse events:
There is two level of adverse events:
1. Reporting
# Reporting
2. Investigation.
# Investigation.
Conclusion: Focus on the reporting part of adverse events.
Conclusion: Focus on the reporting part of adverse events.
There are some adverse events reports that are mandatory on the national level in Switzerland.
There are some adverse events reports that are mandatory on the national level in Switzerland.
Line 73: Line 73:


Number regarding adverse events:
Number regarding adverse events:
According to Leonidas only 10% of the reaction are being reported in Greece.
# According to Leonidas only 10% of the reaction are being reported in Greece.
In Portugal and Greece the doctors are the main source of the adverse events reports.
# In Portugal and Greece the doctors are the main source of the adverse events reports.
In the Netherlands the patients are also contributing to the reports.
# In the Netherlands the patients are also contributing to the reports.
In Austria the adverse events are not on the agenda. Hospitals have some things organised but the topic is not present due to other prioritisations.
# In Austria the adverse events are not on the agenda. Hospitals have some things organised but the topic is not present due to other prioritisations.


Links naar documenten
Links naar documenten

Revision as of 03:04, 14 September 2022

Agenda

Meeting Venue

Montreux

9:30 Welcome

  • Review and Approve Agenda

11:00 - 13:00 House keeping

  • Planning of new season 2022-2023
  • Membership status
  • Co-chair positions & elections
  • DCC reporting
  • Approve NWI proposals

13:00-14:00 Lunch

14:00- 15:30 Supply

15:30- 16:00 Break

16:00- 17:30 Supply

- Supply To do’s on supply: We’ll work in R4B, and descope the Inventory part, explaining that this is due to HL7 FHIR not having the resources. 1. Identify the use cases that we want to publish in the IG 2. Convert those use cases to the IG 3. Add narrative pages for scope/disclaimer (i.e. Relation with inventory) 4. Document Actors o Requester o Request Filler o Receiver o Supplier 5. Document transactions o Resupply Request o Resupply Response o Delivery Notice o Receipt notice 6. Check and review the Logical Models 7. Create Profiles o Resupply Request o Resupply Response o Delivery Notice o Receipt notice 8. Create examples 9. Create testing specifications

Links naar documenten (o.a. whitepaper) https://build.fhir.org/ig/IHE/pharm-supply/ White paper: https://www.ihe.net/uploadedFiles/Documents/Pharmacy/IHE_Pharmacy_WP_Supply.pdf


18:00 Adjourn

Agenda woensdag


- Adverse events There is two level of adverse events:

  1. Reporting
  2. Investigation.

Conclusion: Focus on the reporting part of adverse events. There are some adverse events reports that are mandatory on the national level in Switzerland. Conclusion: There is a need for adverse events on the national level. WHO want to give this more priority Action: we should ask the WHO to support the development of the logical data model for adverse events. OPEN IHE to support the transaction. Physicians are afraid that if they do the reporting they also need to do the investigation See an example of the Greece yellow carte: https://www.eof.gr/assets/KITRINI_KARTA.pdf

Number regarding adverse events:

  1. According to Leonidas only 10% of the reaction are being reported in Greece.
  2. In Portugal and Greece the doctors are the main source of the adverse events reports.
  3. In the Netherlands the patients are also contributing to the reports.
  4. In Austria the adverse events are not on the agenda. Hospitals have some things organised but the topic is not present due to other prioritisations.

Links naar documenten

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