Development
Roadmap product development
Work is in progress to extend the Clinical Rules based on recommendations from and prioritization
by the expert group. Recommendations resulting from contra-indications and interactions in the National (G)-Standard are modeled as Clinical Rules. Other (self made) standard protocols are eligible for this as well.
 Developing multiple integrated modules for different users:
- Module for the prescribing physicians (EPS)
- Administers module
- Several primary care modules
Extending sources:
- INR
- Genotyping
- Signals from clinical chemistry
At the moment Pharmaps is in the process of scaling up to an international level. From a technical point of view, Pharmaps Medication Safety Plus can easily connect to other laboratory and medication systems. Due to contacts with international pharmacists, hospitals and consultants, we see good international opportunities to solve problems and offer solutions.
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