We want to carry out an investigation into the state of medication safety in the Netherlands. This research consists of a main study and three sub-studies:
1. medication transfer
2. optimize drug use in the elderly
3. patient guidance
We have divided this tender into 2 plots, namely:
- lot 1: carrying out the main research and partial examination 1
- lot 2: carrying out substudies 2 and 3.
Main study 'Medication safety in the Netherlands' and partial study 1 'Medication transfer'Before 1 April 2024, we expect a main report that provides insight into the current state of medication safety in the Netherlands, the effects of the current policy and makes suggestions regarding new policies. In addition to the main report, we expect an overall summary report before 1 April 2024 and one independently readable and useful report for partial research 1: medication transfer;
As part of partial research 1 (medication transfer), we expect that a measuring instrument will also be delivered.
The main report and subreport 1 should be the result of an investigation:
- That answers research questions asked.
- That provides a useful approach for future measurements in the field of medication transfer.
- That there is a clear organization with a single point of contact for the management GMT.
- The results of which have been discussed with a guidance committee appointed by us and are widely supported.
- Whose methodology and associated limitations are clear and transparent.
- This is carried out by a permanent research team, whether or not from different parties to 1 Contractor per plot, which has a wide range of relevant knowledge and experience.
- That is carried out in an efficient manner.
- This is carried out in a way that contributes to the goals of the Government in the field of socially responsible commissioning and procurement.
Substudy 2 “Optimizing drug use in the elderly” and partial study 3 “Patient guidance.”Before 1 October 2023, we expect two independently readable and actionable reports for sub-research 2: 'Optimizing drug use in the elderly' and partial research 3:
“patient guidance.”
The subreports should be the result of an investigation:
- That answers research questions asked.
- That provides a useful approach for future measurements in the field of medication transfer.
- That there is a clear organization with a single point of contact for the management GMT.
- The results of which have been discussed with a guidance committee appointed by us and are widely supported.
- Whose methodology and associated limitations are clear and transparent.
- This is carried out by a permanent research team, whether or not from different parties to 1 Contractor per plot, which has a wide range of relevant knowledge and experience.
- That is carried out in an efficient manner.
- This is carried out in a way that contributes to the goals of the Government in the field of socially responsible commissioning and purchasing.