Alvita is Alliance Healthcare’s own label brand of competitively priced, high quality patient care products.
The comprehensive range is exclusively available to independent pharmacists across Europe, and comes with the delivery expertise of Alliance Healthcare.
At Alvita, we believe that essential patient and personal care products should be available to everyone at an affordable price, without compromising on quality.
That’s why we carefully and ethically source our products from reputable manufacturers and bring to you a range of pharmacy quality alternatives to leading brands at affordable prices.
This means customers and patients can find everything for their healthcare needs under one roof - your pharmacy.
Alvita is currently present in 7 countries: France, United Kingdom, Spain, Italy, Germany, Portugal and Turkey.
Why choose Alvita?
High quality products, sourced from reliable suppliers with strong ethical standards.
Competitive trade prices to keep costs low for both pharmacy and customer.
Working exclusively with Alliance Healthcare enables pharmacists to benefit from a same or next day delivery service.
About our products - Medical Device Regulation (MDR)
Starting from 26th May 2021, the new Medical Device Regulation (MDR) replaces the Medical Device Directive (93/42/EEC) and Directive on Active Implantable Medical Devices (90/385/EEC) in the European Union.
The new MDR ensures better protection of public health and patient safety and more transparency. A comprehensive EU database on medical devices (EUDAMED) will contain a picture of all products being available on the EU market and a large part of the information will be made publicly available. Also a new device identification system based on a unique device identifier (UDI) will allow easier traceability of medical devices.
With the full implementation of the MDR that governs the production and distribution of medical devices, compliance is mandatory for all companies that are bringing CE marked products to the market.
We are MDR ready
At Alvita, we are confident that we can supply our customers with CE marked products in compliance with the regulatory framework at the time of supply.
We are MDR ready and have a fully compliant class I portfolio. For Class Is or higher medical devices, we will be implementing MDR changes as long as the MDR CE certificates are granted which means until 26th May 2024 at the latest.