Om oss
Built for quality-focused pharmaceutical operations
Established in 2024 as part of the Chemtronica group, Pharmtronica AB was created to focus on authorised magistral manufacture and future pharmaceutical service areas. Our work is built around clear procedures, trained personnel, documented processes, and strong quality oversight.
Who we are
Pharmtronica AB combines a dedicated pharmaceutical focus with the support of an established business foundation through the Chemtronica group. From our site in Stockholm, we operate under a permit for Magistral Manufacture granted by the Swedish Medical Products Agency, LMV.
Our current operations are built around quality, compliance, and reliable execution, with a focus on controlled pharmaceutical activities, documentation, traceability, and quality review. We are also developing future capabilities in contract manufacture and API supply, which will only be offered when the required regulatory, quality system, and compliance requirements are fully in place.
What we do
Our business is centred around one current authorised area and two future service areas under development:
Magistral Manufacture
Patient-specific magistral preparations carried out under controlled non-sterile preparation processes, with pharmacist involvement, documented procedures, quality review, and defined release steps.
Contract Manufacture
Future service area under development. Pharmtronica is developing future capabilities for selected non-sterile pharmaceutical manufacturing activities, including formulation-related operations, packaging, labelling, and batch documentation. This service will only be offered when the required GMP, quality system, and regulatory requirements are fully in place.
API Supply
Future service area under development. Pharmtronica is developing future capabilities related to API and pharmaceutical raw material sourcing, import, handling, and supply support. This service will only be offered when the required regulatory, quality, and compliance requirements are fully in place.
Professional expertise
Our team includes pharmacists, quality leadership, and trained personnel across production, supply chain, administration, IT, and site operations. Roles and responsibilities are clearly defined, and training is a core part of how we work. For quality-related roles and controlled activities, training is documented and reviewed regularly to maintain competence and oversight.
Quality and compliance
Quality is part of daily work at Pharmtronica, not a separate step at the end. Our quality system is designed to support safe, controlled, and traceable pharmaceutical operations. It includes documented procedures, preparation records, material checks, supplier qualification, risk management, deviation handling, change control, training, and self-inspection.
Our facility
The facility supports goods receipt, material handling, production preparation, packaging, storage, dispatch, and controlled cleanroom-based activities. The site includes dedicated working areas such as Grade D cleanroom space, secondary packaging areas, and controlled flows for personnel and materials.
Vision, values and culture
Our vision is to contribute to safe and reliable pharmaceutical supply through quality-driven operations and responsible pharmaceutical work. Our values are rooted in professional accountability, scientific discipline, documentation, traceability, and respect for the responsibility that comes with pharmaceutical activities.
We promote a culture where quality is part of everyday practice, where trained professionals take ownership of their roles, and where continuous learning and ethical collaboration support long-term trust.
Get in touch
Get in touch with Pharmtronica AB for service enquiries, partnership discussions, or further information about our operations.