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.
Why work with the manufacturer
Formulation, production and documentation sit with one manufacturer.
- Own laboratories
- Every IVIXIR formulation is developed in EFBA's own laboratories.
- Batch traceability
- Production batches are recorded and traceable.
- Batch documentation
- Certificate of analysis for each batch and stability documentation, shared with qualified partners on request.
- Registration partnership
- Licensed local partners apply for registration; 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, with one set of documents.
What we manufacture
The IVIXIR series: ten IV vitamin and nutrient formulations, listed in the catalogue by active ingredients (generic name), brand and presentation.
Who the catalogue is for
The catalogue is intended for licensed healthcare professionals, hospitals and licensed healthcare facilities, and licensed pharmaceutical importers and distributors. 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.
- Registration partners
- Licensed local companies that can apply for product registration.
How a partnership enquiry works
Every step is handled in writing, and nothing is offered to the general public.
Enquiry
Choose the products of interest and send the request.
Verification
We confirm your licenses 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.
What documentation is available to partners?
A certificate of analysis for each batch, stability documentation and technical documentation for the registration dossier, shared with a verified licensed partner on request.
Who applies for registration in the Philippines?
A licensed local importer or distributor holding a License to Operate (LTO) from the Food and Drug Administration (FDA) Philippines applies for the Certificate of Product Registration (CPR). EFBA, as the manufacturer, provides the technical documentation and works with that partner.
Who can send an enquiry?
Licensed pharmaceutical importers and distributors, 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.