The University Hospital Aachen (UKA) plans to continue the expansion of digitization in the field of the digital medication process. As part of this measure, an additional area for the supply of medicines "Unit-dose" is to be created in the supply building.

A feasibility study was first carried out on the above-mentioned construction project. In it, the variants of the development were presented and evaluated and the financial and scheduling framework of the measure was examined. In addition, a technical and structural assessment of the scope was carried out. Commissioning is planned for the end of 2024.

Due to the planned scope of services and the nature of the essential services as a "room-in-room solution" (alternatively: conventional construction), the implementation of a planning competition is gladly carried out for economic and functional reasons. §78 VgV.

An open procedure is often used as a type of procedure for commissioning an efficient planning office. §15 VgV for the four lots.

It is possible for a bidder to apply for both one lot and several lots. There is no offer or surcharge limit according to §30 Abs. 1 VgV.

The subject of this VgV award procedure are the following service profiles (including special services) - divided into four lots:

- Lot 1 "Object Planning Building". §34 in conjunction with Annex 10 HOAI 2021 in LPH 1 to 8, plus special services

- Lot 2 "Fachplanung Tragwerkplanung". §51 HOAI in conjunction with Annex 14 HOAI 2021 in LPH 1 to 6

- Lot 3 "Technical Equipment Planning". §55 in conjunction with Annex 15 HOAI 2021 in LPH 1 to 8 for ALG 1 to 5 and 8, plus special services

- Lot 4 "Technical Equipment - Laboratory Planning". §55 in conjunction with Annex 15 HOAI 2021 in LPH 1 to 8 for ALG 7, plus special services

Drug therapy safety is one of the central tasks for the hospital pharmacy. The medication process is an error-prone high-risk process, so single-dose or "unit-dose" drug delivery is considered the safest supply route for hospital patients. The supply of individually packaged drugs is part of an overall concept consisting of electronic prescription with dosing and action testing, automated, patient-related cornmissioning of single doses and IT/barcode-based administration documentation. The primary goal here is to improve the process and quality of patient-specific drug care and, in support of adherence to therapy, in particular to avoid medication errors and relieve the staff on the wards.

The space program of the unit can is specified as follows and consists of:

- a storage area of approx. 50 m2,

- a lock area (material and personnel) of about 30 m2 and

- a cleanroom area of approx. 100 m2 (lowest cleanroom level "D" for GMP laboratories). the connection to the stock and the pharmacy.

The aforementioned clean room is the core area of the "unit-dose". Here, the medicines are unpacked, individually sorted, packaged and labelled and finally checked before they are sent to the wards via the automatic goods transport system. The area places particular demands on temperature, relative humidity, particle concentration and microbiological purity. These conditions are currently not met in the existing supply building.

Drug therapy safety is one of the central tasks for the hospital pharmacy. The medication process is an error-prone high-risk process, so single-dose or "unit-dose" drug delivery is considered the safest supply route for hospital patients. The supply of individually packaged drugs is part of an overall concept consisting of electronic prescription with dosing and action testing, automated, patient-related cornmissioning of single doses and IT/barcode-based administration documentation. The primary goal here is to improve the process and quality of patient-specific drug care and, in support of adherence to therapy, in particular to avoid medication errors and relieve the staff on the wards.

The space program of the unit can is specified as follows and consists of:

- a storage area of approx. 50 m2,

- a lock area (material and personnel) of about 30 m2 and

- a cleanroom area of approx. 100 m2 (lowest cleanroom level "D" for GMP laboratories). the connection to the stock and the pharmacy.

The aforementioned clean room is the core area of the "unit-dose". Here, the medicines are unpacked, individually sorted, packaged and labelled and finally checked before they are sent to the wards via the automatic goods transport system. The area places particular demands on temperature, relative humidity, particle concentration and microbiological purity. These conditions are currently not met in the existing supply building.

Drug therapy safety is one of the central tasks for the hospital pharmacy. The medication process is an error-prone high-risk process, so single-dose or "unit-dose" drug delivery is considered the safest supply route for hospital patients. The supply of individually packaged drugs is part of an overall concept consisting of electronic prescription with dosing and action testing, automated, patient-related cornmissioning of single doses and IT/barcode-based administration documentation. The primary goal here is to improve the process and quality of patient-specific drug care and, in support of adherence to therapy, in particular to avoid medication errors and relieve the staff on the wards.

The space program of the unit can is specified as follows and consists of:

- a storage area of approx. 50 m2,

- a lock area (material and personnel) of about 30 m2 and

- a cleanroom area of approx. 100 m2 (lowest cleanroom level "D" for GMP laboratories). the connection to the stock and the pharmacy.

The aforementioned clean room is the core area of the "unit-dose". Here, the medicines are unpacked, individually sorted, packaged and labelled and finally checked before they are sent to the wards via the automatic goods transport system. The area places particular demands on temperature, relative humidity, particle concentration and microbiological purity. These conditions are currently not met in the existing supply building.

Drug therapy safety is one of the central tasks for the hospital pharmacy. The medication process is an error-prone high-risk process, so single-dose or "unit-dose" drug delivery is considered the safest supply route for hospital patients. The supply of individually packaged drugs is part of an overall concept consisting of electronic prescription with dosing and action testing, automated, patient-related cornmissioning of single doses and IT/barcode-based administration documentation. The primary goal here is to improve the process and quality of patient-specific drug care and, in support of adherence to therapy, in particular to avoid medication errors and relieve the staff on the wards.

The space program of the unit can is specified as follows and consists of:

- a storage area of approx. 50 m2,

- a lock area (material and personnel) of about 30 m2 and

- a cleanroom area of approx. 100 m2 (lowest cleanroom level "D" for GMP laboratories). the connection to the stock and the pharmacy.

The aforementioned clean room is the core area of the "unit-dose". Here, the medicines are unpacked, individually sorted, packaged and labelled and finally checked before they are sent to the wards via the automatic goods transport system. The area places particular demands on temperature, relative humidity, particle concentration and microbiological purity. These conditions are currently not met in the existing supply building.