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Who we work with

Noventure is licensed by the Spanish Agency for Medicines and health Products (AEMPS) as a manufacturer of medical devices. Our Quality Management System is based on ISO 13485 and it has been certified by Notified Body No. 0476. We are also duly registered in the Helath Register of Food Industries and Products (RSIPAC) of Catalonia (Spain).

Noventure's products are manufactured in production plants througouht the European Union, thereby giving us great versatility and flexibility to supply our partners.

All production sites boast advanced technology and highly qualified personnel. They all comply with applicable legislation and are certified in accordance with GMP and/or ISO, essetial requirement for the manufacturing of our products.

The range of products under Noventiure's portfolio includes the following dosage forms:

Oral solids

powders, hard vegetable capsules and coated tablets

Liquid forms

solutions and suspensions

Semi-solid forms


Noventure's specific quality management system is based on ISO 13485:2016, thereby ensuring compliance with the general safety and performance requirements for medical devices (Directive 93/42/EEC and Regulation 2017/745). The system covers all processes, from design through production and supply. Moreover, our Risk Management and Post-Market Surveillance Systems allow us to identify critical points and to gather and analyse data on quality, performance and safety throughout the product lifecycle in order to generate the necessary CAPAs and achieve continuos improvement in quallity and performance. For Food Supplements, Noventure follows the specific regulations thereof regarding food safety, and it ensures that the proper Hazard Analysis and Critical Control Points (HACCP) Plan is implemented and maintained.

Our medical devices boast the CE conformity marking. Noventure´s Regulatory Affairs Department supports partners by coordinating and providing the necessary documentation requested for registration purposes outside of the European Union.

Some of our collaborating centers

Our medical devices have been developed in collaboration with numerous research centers across Europe. The results of their studies have led to a better understanding of the mode of action of the ingredients of our products and the clinical benefits they provide. Basic and experimental research laboratories, as well as clinical hospital departments, have provided essential preclinical and clinical information to back up the indications of our products.

Artwork designers

"The text and graphic coordination of the packaging for your product is supported by either Ms. Linda Rossini or Thinkinpress. They liaise with you during the packaging design from the creation till the regulatory process and approval"
 artwork designers