What we stand for
We at innomedis put highest quality first in order to satisfy our customers. In order to be able to ensure this level of satisfaction, we strictly adhere to European quality standards while setting new standards ourselves which are constantly examined and audited. We strictly define and supervise all concerned processes, choose our suppliers and service providers wisely and make sure they acquaint themselves with our high quality requirements.
Certified in accordance with ISO EN DIN 13485
innomedis AG has been certified as medical product manufacturer in accordance with the applicable quality standards.
We check our suppliers and ingredients during all supply chain management processes, from the originator up to the finished product by attaching special value to the highest quality at any given time.
A continuous supervision of the whole production process is taking place by keeping close contact to our business partners.
Free from preservative properties
We attribute great importance to an unpreserved filling of the products, as many preservatives can cause negative side-effects over a certain period of time.
In order to be able to offer unpreserved products, we use innovative and patented bottle systems such as the OSD (ophthalmic-squeeze-dispenser) or pump bottle systems for our eye drops and sprays.
Service and customer proximity
It is our fundamental aim to exceed our clients´ expectations.
One way of realizing our ambitions is to adapt ourselves quickly and in an easy and flexible way to our clients´ wishes. "The customer is king" - this is not only an empty slogan to us, but the core of our daily work.
We conduct customer surveys on a regular basis in order to learn where our service may be improved.
CE-certified medical product
CE marking is the medical product manufacturer’s claim that a product meets the essential requirements of all relevant European Medical Device Directives and is a legal requirement to place a device or product on the market in the European Union. Our products are all CE-certified, thus they are fully monitored at all stages of the product life cycle. This includes:
- the analysis, evaluation and minimization of all risks and side-effects
- the verification of biological compability
- ensuring that mechanical and electrical safety standards are met
- clinical and diagnostic evaluation
- ensuring therapeutic and diagnostic benefit
- monitoring of measuring consistency