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In Our Office Or Elsewhere Expertise And Reliability Regulatory Affairs
In Our Office Or Elsewhere
We are available to meet our clients in our office or elsewhere
Expertise And Reliability
Over three decades of knowledge, expertise, and reliability at your service
Regulatory Affairs
More and more companies choose to outsource regulatory affairs
Regulatory Consultants

Di Renzo Regulatory Affairs is a leading company in the field of regulatory consulting, with nearly 40 years of experience. The services offered concern human and veterinary medicines, medical devices, food supplements, cosmetics, biocides, PMCs and all related products.

There are also special units dedicated to pharmacovigilance, devicevigilance, cosmetovigilance, scientific information, quality management systems, and many other aspects of regulatory management. 

Characterised by a strong international organisation, our company cooperates with many regulatory consultants in every EU country and in the most important extra-EU countries.

Thanks to its relevant know-how gained over time, and with its organisation made up of more than 100 graduated experts with medical and scientific training, Di Renzo Regulatory Affairs can offer appropriate and prompt indications, strategies and services on each of the above areas of interest

Medicines for Human Use

Our services for Human Medicines

Medicinali Veterinari

Veterinary Medicines

Our services for Veterinary Medicines

Dispositivi Medici

Medical Devices and IVD

Our advice to manufacturers and distributors

Biocidi e Disinfettanti

PMC and Biocides

Services aimed at companies producing PMC and Biocides


Our experts at the service of cosmetic companies

Integratori Alimentari

Food supplements

Consultancy for manufacturing and importing companies

Di Renzo Regulatory Affairs started their activity in 1985, and has developed their own organisation since, then upgraded to an international level. The many experts working in our company are mostly graduated in science: chemistry, medicine, pharmacy, pharmaceutical technologies, engineering, biology, biotechnology, statistics and other.   

As of 2019, Di Renzo Regulatory Affairs has moved to new operative headquarters, still located in Rome but larger and best suited for the many complex activities we perform. Our office is close to the Italian Ministry of Health, to the AIFA (Italian Medicine Agency) and to the High Health Institute (ISS).

Di Renzo Regulatory Affairs has also two more offices, one in Milan and the other in London.

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From Our Blog
Registrazione DM nel database ministeriale
16 July , 2024

Registration of medical devices in the database of the Italian Ministry of Health

Di Renzo Regulatory Affairs Comments (0)

21 May , 2024

Pharmacovigilance: in-house or outsourced? Challenges and opportunities for pharmaceutical companies in the era post-Directive 2010/84.

Di Renzo Regulatory Affairs Comments (0)

Serializzazione e tracciabilità
14 May , 2024

Serialization, state of the art

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