The efficacy and safety of medical devices is based on the exhaustive literature reviews performed by the leading specialists in the fields of pharmacology and health care.
The development and manufacturing of medical devices in Pharmia is conducted according to the regulatory authorities and our certified ISO 13485 quality management system.
Our operations are inspected regularly by Notified Bodies and pharmaceutical companies. Every medical device has a CE-mark to ensure the product efficiency and safety and fulfillment of regulatory requirements.
We are actively following the development of active raw materials, product innovations and regulatory requirements in order to create and maintain state-of-the-art products. Over the years, we have developed a good cooperation relationship with the authorities.
Several indication areas and product variations
At the moment Pharmia has several medical devices under manufacturing and the end of product development phase. Products are intended for:
- Treatment of common cold
- Treatment of sore throat
- Treatment of dry nose
- Relieving the gastric symptoms
- Relieving dry mouth