IV vitamin manufacturer for licensed partners
EFBA develops and manufactures the IVIXIR series of IV vitamin and nutrient formulations and works directly with licensed importers, distributors and healthcare facilities.
- Manufacturer-direct contact
- GMP-certified manufacturing
- Batch documentation on request
Why work with the manufacturer
- Own laboratories. Every IVIXIR formulation is developed in EFBA's own laboratories.
- GMP-certified manufacturing. Production under GMP-certified manufacturing conditions.
- Batch documentation. Certificate of analysis for each batch, GMP certificate and stability documentation, shared with qualified partners on request.
- Registration partnership. Licensed partners lead registration locally; EFBA prepares the technical documentation.
- Cold chain. Storage and transport conditions defined for each product and set out in the documentation.
- One range, one manufacturer. Ten formulations from a single manufacturer.
What we manufacture
EFBA manufactures the IVIXIR series: ten IV vitamin and nutrient formulations with names, volumes and active ingredients listed in the catalogue. View the IVIXIR catalogue (for healthcare professionals).
Product names are trade names.
Who we work with
Importers and distributors
Licensed pharmaceutical importers and distributors with established cold-chain handling.
Hospitals and licensed healthcare facilities
Hospitals and licensed healthcare facilities that source through a licensed supplier.
Product Registration Holders
Companies registered locally that can submit a product for registration.
How a partnership enquiry works
Enquiry
Choose the products of interest and send the request.
Verification
We confirm your licences and your role in the supply chain.
Documentation
We share the manufacturer's documentation for review.
Reply in writing
We reply in writing with the next step.
Manufacturer FAQ
Who manufactures the IVIXIR series?
EFBA develops and manufactures every IVIXIR formulation in its own laboratories, under GMP-certified manufacturing conditions.
What documentation is available to partners?
A certificate of analysis for each batch, GMP certificate, stability documentation and technical documentation for the registration dossier, shared with a verified licensed partner on request.
Who registers and imports the products in Malaysia?
A locally registered Product Registration Holder submits the product to the Drug Control Authority through NPRA, and a licensed importer holds the import licence. EFBA, as the manufacturer, provides the technical documentation and works with those partners.
Who can send an enquiry?
Licensed pharmaceutical importers and distributors, Product Registration Holders, hospitals and licensed healthcare facilities. This website is not intended for the general public.
Send a partnership enquiry
Choose the products of interest on the quote request page and tell us about your business. We reply in writing.