Mednex Supplies works under third-party manufacturing agreements with qualified pharmaceutical manufacturers, selected according to product requirements, regulatory expectations, manufacturing capability and market needs. Our partners provide the dossiers and documentation required for product registration.
Manufacturing capabilities aligned with applicable WHO-GMP requirements and quality standards.
Access to qualified manufacturing facilities operating according to relevant European GMP standards.
Specialized manufacturing support for complex injectable oncology pharmaceutical products.
Capabilities covering sterile and lyophilized formulations for specialized pharmaceutical requirements.
Tablet and capsule manufacturing capabilities supported by qualified pharmaceutical production partners.
Manufacturing partners are selected according to individual product, regulatory and target-market requirements.