One partner for any service: you can choose Zeta for an all inclusive service as we track your product from the development of the formulation to the packaging and distribution, or rely on us for a specific activity. In any case, you will be assisted with the quality that only a very experienced pharmaceutical group can provide. This is what we mean for tailored service.
PRODUCT DEVELOPMENT AND FORMULATION
EXPERIENCE AND INNOVATION
Medicines, medical devices, cosmetics, dietary supplements. Our R&D can help you formulate your product, for all types of administration or application for which we are competent. Thanks to our wide experience in all these sectors, we can suggest a lot of suggestions that are innovative, often surprising, always effective. Working with cosmetics and dietary supplements means that we are highly sensitive to the organoleptic characteristics of products. Just as important as the technical characteristics.
ANALYSIS DEVELOPMENT
PROFESSIONAL TECHNOLOGY IN OUR LABORORATORIES
Our laboratories have the latest instruments. And we have all the competencies required to develop and validate methods of analysis, whether for analysing new products or to update methods for products already on the market. In addition to the classic methods, we have acquired considerable know-how in the development of methods for titrating probiotics, even for multi-strain products.
PACKAGING DEVELOPMENT
NEW IDEAS LEAD TO NEW SOLUTIONS
In packaging, too, we have specific, qualified competence. We are constantly selecting packaging solutions and suppliers in Italy and in Europe, so we can offer you, too, new ideas. Lastly, we can give you a lot of help with graphic design, thanks to the experience and talent of our graphic design office.
REGULATORY AFFAIRS
EXPERIENCED IN 5 DIFFERENT REGULATORY FIELDS WITH INTERNATIONAL KNOWLEDGE
Another strong point of Zeta Farmaceutici Group is our regulatory affairs office. there are 5 regulatory areas (pharmaceuticals, medical devices, cosmetics, dietary supplements, biocides), for various countries in Europe and elsewhere. We can draw up for you the dossier of a drug in CTD format, documentation for notifying regulatory changes, preparation of documentation required by the appropriate regulations (Product Information File, Technical Data File etc.).
PRODUCTION OF SAMPLES FOR CLINICAL TESTING
RELIABLE SUPPORT
The Zeta Farmaceutici factory is authorised for the production of samples for clinical testing of liquids for internal use and liquids for external use. This is not our core business, but we have never said no, when clients have asked us to help them in this activity, for example, for registration of an antihistamine medicine.