We are a CDMO in the field of Medical Devices.
Our activity is mainly focused on the production and asepsis distribution of sterile liquid products and in particular on packaging in small containers of different capacities.
We are constantly engaged in the development and production of innovative formulations in the field of substance-based medical devices.
Enable Innovations is ISO 13485:2021 certified.
We recently obtained the CE certificate for our eye drops line according to the new MDR 2017/745 for Medical Devices.
The activity of Enable Innovations is primarily focused on the preparation and filling in aseptic conditions of sterile liquid products and in the packing into small plastic containers of different volumes. Enable Innovations is active in the field of medical devices, food supplements and foods for special medical purposes.
Enable Innovations S.r.l. was founded in 2009 with the aim to study and develop new and innovative products in the field of Pharma and Medical Devices so as to improve the state of the art both for the patients and for the specialists.
We turn the customer’s idea into a finished product and also provide contract manufacturing of formulations according to customer requirements.
We listen to the customer’s request
for the formula to be developed.
Thanks to our in-house laboratories and collaboration with several external laboratories, we are able to carry out all the necessary activities for product development, such as formulation studies, pilot batch and stability studies.
In our state-of-the-art, fully-automated production lines, the bulk preparation, distribution and packaging of the product takes place.
We offer products and services with high quality standards.
Enable Innovations has been operating since 2009 following rules that lead to quality and certified products.