Eurolab Aseptic Services Unit,
Leading the Way in Sterile Processing
Our advanced sterile cGMP facility ensures the highest standards in producing safe and effective Oncology and Ophthalmic treatments, improving access to quality care for patients who need it most.
EUROLAB ASU
Our quality commitment is resolute and includes implementing Good Manufacturing Practice (GMP) across all our processes.
Located in Midrand, Johannesburg, and with a core business focus on world class cGMP sterile manufacturing, Eurolab’s Aseptic Services Unit (ASU) offers three key services. Firstly, the centralised mixing services of sterile medicines, secondly, the manufacture of biologically based advanced therapeutic medicines, and thirdly, the production of sterile clinical trial material. It is South Africa’s first centralised mixing facility which also meets international standards. This flagship Eurolab facility is aligned with top facilities in the United Kingdom, Europe and Australia and in South Africa, and is offering significant benefits to oncologists, ophthalmologists and their patients to make the treatment process efficient, safe and quick – and more affordable.
WHY CHOOSE US
Benefiting oncologists, Ophthalmologists and their patients
Ready to use
medicine
Reduction in
medication errors
Ongoing security of oncology and ophthalmic medicine supply
Mitigation of health and safety risks associated with the dosing and handling of chemotherapy medicines
Each product is issued with a
certificate of compliance
(COC) for sterility
Extended stability allows for
centralised admixing and
administration at infusion
sites and home- based care.
OUR CLIENTS
who we serve
Doctors
Doctors who want their patients to access sterile oncology and ophthalmic compounding medicines which meets international best practice quality and safety standards.
Clinical Trial Sponsors
Clinical trial sponsors and principle investigators requiring compliance to international best practices for sterile admixing as set out in USP 797 ensuring quality and safe oncology medicines.
Contract Manufacturers
Contract manufacturers who can use our world class GMP-approved facility for contract manufacturing.
Medical Schemes
Medical schemes seeking optimal efficiency for expensive medicines
Doctors
Doctors who want their patients to access sterile oncology and ophthalmic compounding medicines which meets international best practice quality and safety standards.
Clinical Trial Sponsors
Clinical trial sponsors and principle investigators requiring compliance to international best practices for sterile admixing as set out in USP 797 ensuring quality and safe oncology medicines.
Contract Manufacturers
Contract manufacturers who can use our world class GMP-approved facility for contract manufacturing.
Medical Schemes
Medical schemes seeking optimal efficiency for expensive medicines
our equipment
Specialised Equipment
Our fully validated facility is compliant to cGMP (Manufacture of Sterile Medicinal Products) as set out in the SA Guide to Good Manufacturing Practice for Medicines. It encompasses:
- A GMP-approved cleanroom with biosafety cabinets (Grade A) in a Grade B background environment
- Specialised cameras which ensure photographic evidence of each admixed product and forms part of the documented evidence to ensure complete batch traceability
- Fully validated, innovative rapid microbiological testing technology which provides sterility confirmation within 4 hours, allowing for the release of product within 24 hours.