Compounding
pharmacies

Whether production is carried out with or without a manufacturing authorisation, under a safety cabinet or in an isolator—cytostatic production places the highest demands on safety, containment, and process organisation. Which technical and regulatory framework conditions must be considered? Which solution is cost-effective and, at the same time, future-proof?
Together with you, we develop a tailored concept—based on multidisciplinary experience in planning, cleanroom technology, containment, and regulatory consulting. This creates safe manufacturing environments that protect personnel, ensure product quality, and meet all legal requirements.

How large does the warehouse need to be? Which products may be stored together? What requirements apply to the proper storage of medicinal products? And is a fully or partially automated system the right solution? We support you with a structured analysis of your requirements—from capacity and material-flow assessments and regulatory specifications through to the selection of suitable storage and picking systems.
On this basis, we develop cost-effective and future-proof concepts and support you during the implementation phase as well—for efficient workflows, transparent processes, and safe pharmaceutical logistics.

Which unit-dose system best meets your requirements? How should deblistering, inspection, and pouch repair be organised? Which materials must be kept available in the room—and how can routes be designed efficiently and ergonomically? We support you with the end-to-end planning of your unit-dose area—from layout development and the preparation of robust tender documents through to the technical evaluation of bids. We are also at your side during implementation: from the fit-out of the premises to acceptance of the systems and equipment. The result is a cost-effective, process-reliable, and future-ready solution for patient-specific medication supply.

The manufacture of extemporaneous and stock preparations is, in accordance with the German Pharmacy Operating Regulations (ApBetrO), an integral part of every pharmacy. Accordingly, the requirements for premises, equipment, and organisation are high.
We support you in planning and implementing suitable manufacturing areas—practical, standards-compliant, and efficient. From functional room zoning and utilities and ventilation concepts through to structural implementation, we develop solutions that optimally support your day-to-day operations and meet regulatory requirements.

Safety cabinet or isolator? Does the use of a compounder make sense—and how can it be safely integrated into an isolator system? With terminal sterilisation, the question also arises as to the appropriate autoclave concept. And which cost-effective solution is suitable for filling small campaigns? Planning sterile manufacturing areas requires a balanced interplay of regulatory requirements, process understanding, and technical implementation. Together with you, we analyse the requirements and develop a tailored concept—from layout planning and the selection of suitable technologies through to defining the interfaces.