DR International is a regulatory consulting firm for companies that market or produce medicinal products for human and veterinary use, cosmetics, medical devices, biocides and food supplements. Our task is to guide companies through the current legislation and successfully meet the demands of our clients.
Over its thirty years of experience Di Renzo Regulatory Affairs has expanded its departments by opening new sectors required by the market. The demands of the pharmaceutical companies have prompted us to open up to the international market by setting up new offices and hiring new staff.
About sixty of the employees and consultants are part of DR International, to assists the company before and after the product is placed on the market, from a regulatory point of view. We manage every aspect of the process, from feasibility assessment to marketing.
Our experiencecovers severalareas such as:
We have experience in both the domestic and the international arena thanks to the collaboration of a network consultants and we are able to assist clients in all phases of the life cycle of the product.
By maintaining the highest professional standards and focusing on the qualifications of our staff, we are able to guarantee our clients a quality service. We continuously strive to meet the deadlines of projects that companies entrust us with, ensuring the integrity of sensitive data that we handle.
We rely on all our employees, who undergo constant training, to keep abreast of all new rules and regulations.
The DR International team is multilingual, (English, French, Spanish, Portuguese, German, Chinese, Greek and Italian) which allows us to communicate with our clients from all over the world, with authorities and consultants, reducing misunderstandings and the loss of time.