Magistral Manufacture

We provide patient-specific magistral manufacture under a permit granted by the Swedish Medical Products Agency, LMV. Our magistral manufacture is carried out through controlled non-sterile preparation processes and focuses on preparing prescribed products in accordance with applicable requirements. The work is supported by pharmacists, quality-responsible oversight, and documented procedures for preparation, review, and release.

Our magistral manufacturing service is designed for patient-specific preparations, with a focus on controlled handling, accurate documentation, and quality review before release. Raw materials and packaging materials are checked before use, manufacturing is performed according to approved instructions, and final review is carried out before dispatch. This helps ensure that each preparation is handled with care, consistency, and traceability.

Contract Manufacture

Future service area under development.

Pharmtronica is developing future contract manufacturing capabilities for selected pharmaceutical products, including non-sterile liquid and semi-solid formulations, as well as defined packaging and labelling activities. This service area is currently under development and will only be offered when the required GMP, quality system, and regulatory requirements are fully in place.

The planned contract manufacturing service is intended to support partners who need a reliable and quality-focused manufacturing setup for selected products. The future scope may include controlled receipt of materials, defined processing steps, identity testing or basic quality control where applicable, repackaging, primary and secondary packaging, labelling, and batch documentation. These activities are being designed around structured GMP-aligned principles, with clear operational and quality responsibilities.

API Supply

Future service area under development.

The planned API Supply service is intended to support authorised professional partners through controlled sourcing, import, sampling, identity verification, and repackaging activities where permitted. The service is being designed around traceability, quality oversight, documentation, and defined technical and quality arrangements to support reliable material handling throughout the supply process.