GxP
Specialist & Business Support
Specialist support that unlocks the next step.
MEIA Consulting provides regulated responsible functions such as RP, QP and LMA, support with Swedish R&D tax relief, coordination of requisition-based medicines, and commercial support – specialist roles your business requires but rarely carries on its own.
Some roles are the precondition for the entire business: no LMA, no pharmacy; no RP, no wholesale; no QP, no batch release. MEIA Consulting makes it possible to staff regulated specialist roles flexibly – while freeing up time and capital through services such as R&D tax relief and working medicines logistics.
What we do
Responsible functions: RP, QP and LMA
Regulated roles such as Responsible Person (GDP), Qualified Person (GMP) and the Swedish pharmacy role läkemedelsansvarig (LMA) – staffed with experienced specialists, at the level your operations require.
R&D tax relief (FoU-avdrag)
Support in identifying, documenting and applying for the Swedish research and development payroll relief for staff working in R&D – an opportunity many Life Science companies do not use to its full extent.
Coordination of requisition medicines
Practical coordination of requisition-based medicines between care providers, pharmacies and suppliers – with working procedures for ordering, delivery and follow-up.
Commercial support
Sales and market support for companies in the pharmacy and Life Science sector, built on commercial experience from the industry.
Frequently asked questions
What does a läkemedelsansvarig (LMA) do?
The LMA is responsible for ensuring a Swedish community pharmacy complies with applicable regulations: that self-inspection works, that deviations are handled and reported, and that operations are conducted lawfully. MEIA can provide the LMA function when the pharmacy lacks its own.
What is the difference between RP and QP?
A Responsible Person (RP) is required for wholesale distribution of medicines under GDP and is accountable for distribution compliance. A Qualified Person (QP) is required in manufacturing under GMP and is responsible, among other things, for batch release.
Can we engage a responsible function part-time?
Yes. Many organisations need the function but not full-time. We size the engagement to your operations and risk profile, with clearly defined responsibility and presence.
What is required to qualify for Swedish R&D tax relief?
Staff must work with systematic research or development as defined by the relief, and the work must be correctly documented. We help you assess eligibility and prepare the supporting documentation.
Relevant forLife SciencePharmaciesHealthcare & care