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Who we work with

Noventure is licensed by the Spanish Medicines Agency (AEMPS) as a manufacturer of medical devices and has ISO 13485 certification, granted by Notified Body No. 0476, guaranteeing the required standards of manufacturing.

Our products are manufactured in production plants across the European Union, thereby giving us great versatility and flexibility in supplying our partners.

All production centers boast advanced technology and highly qualified personnel. They comply with applicable legislation with GMP and/or ISO certification, an indispensable requirement for manufacturing our products.

Our range of products includes the following dosage forms:

Oral solids

powders, hard gelatin capsules and coated tablets

Liquid forms

solutions and suspensions

Semi-solid forms


Our quality control system, based on ISO 13485:2003, ensures compliance with the regulatory requirements for medical devices (Directive 93/42/EEC), and covers all processes from production through to customer service. Our risk management and monitoring systems allow us to identify the critical points in the processes and carry out post-market analysis. We can gather and analyze data on quality (incidences and complaint management), performance (post- marketing clinical follow-up) and safety (incident and adverse event management) throughout the product lifecycle. Our focus is always on product safety and continual improvement.

Our products boast CE conformity marking. Our Regulatory Affairs department supports our partners by coordinating and providing the necessary documentation for registration outside 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