enable innovations

Medical Innovation & Healthcare Solutions.

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.

Our Services

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.

Chemical-physical and microbiological analysis of raw materials, semi-finished and finished products

Development of chemical and microbiological analytical methods of raw materials and semi-finished products

Analytical methods validation

Aseptic production processes validation

Microbiological analyses in an aseptic environment

about us

Creation of Innovative Medical Products

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.

Working Process

We turn the customer’s idea into a finished product and also provide contract manufacturing of formulations according to customer requirements.

step 1

We listen to the customer’s request
for the formula to be developed.

step 2

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.

step 3

In our state-of-the-art, fully-automated production lines, the bulk preparation, distribution and packaging of the product takes place.

private label

Finally, we have a wide range of products already certified and available for distribution.



We offer products and services with high quality standards.

DDM 93/42/CEE (and Italian transposition D.L. n. 46 del 24/02/97)

Regulation (UE) 2017/745

Directive 2007/47/CE (e D.L. n. 37 del 25/01/2010)

European Pharmacopoeia


UNI CEI EN ISO 13485:2021

Quality assurance and control

Key Points

Key Points

Enable Innovations has been operating since 2009 following rules that lead to quality and certified products.




Manufacturing Flexibility

Understanding customer’s requirements and turning his idea into a nished product

Lab tests and release for sale

ICH and on-going stability studies according to ICH guidelines

Full service, from formulation and preparation of the bulk through to the nished product

We do not offer only a service or a supply but a supportive and loyal partnership

Test runs and productions for clinical trials


Want more information
about what we do?

Enable Innovations


Via Claudio Tolomeo 20/4
41012 Carpi (MO) – Italy

Office Hours

Mo – Fr     08:30 – 17:30

Sa – Su      Closed

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The contents of this website is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice because of something you have read on this website. This website does not recommend or endorse any specific tests, physicians, medical products, procedures, opinions, or other information that may be mentioned on the Site. The site and its contents are provided on an “as is” basis by the public communication department of Enable Innovations S.r.l.

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