Regulatory Affairs
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Over the years, RAFARM has established with customers and regulatory authorities a reputation for performance, professional integrity and quality of services.
Our Regulatory affairs department is always ready to respond to business challenges, as it has high technical know-how and experience and it acts with speed and agility.
Our Regulatory Affairs team is constantly monitoring the local and international pharmaceutical legislation in the territories of interest and by combining the scientific background with the commercial interest, it contributes to the company decision making from the development until the marketing of the product.
Our Regulatory team of experts supports our partners by advising on legal and scientific requirements and by collecting and evaluating scientific data, giving strategicand technical advice at the highest level, making an important contribution both commercially and scientifically to the success of your projects.
RAFARM Regulatory Affairs department ensures the compilation of high-quality medicinal dossiers and secures speed in the interaction with Health Authorities and third parties for the granting and maintaining of the marketing authorizations of pharmaceutical products.
>1,100 active pharmaceutical licenses worldwide
>1,100 active pharmaceutical licenses worldwide
Over the years, RAFARM has established with customers and regulatory authorities a reputation for performance, professional integrity and quality of services.
Our Regulatory affairs department is always ready to respond to business challenges, as it has high technical know-how and experience and it acts with speed and agility.
Our Regulatory Affairs team is constantly monitoring the local and international pharmaceutical legislation in the territories of interest and by combining the scientific background with the commercial interest, it contributes to the company decision making from the development until the marketing of the product.
Our Regulatory team of experts supports our partners by advising on legal and scientific requirements and by collecting and evaluating scientific data, giving strategic
and technical advice at the highest level, making an important contribution both commercially and scientifically to the success of your projects.
RAFARM Regulatory Affairs department ensures the compilation of high-quality medicinal dossiers and secures speed in the interaction with Health Authorities and third parties for the granting and maintaining of the marketing authorizations of pharmaceutical products.
>1,100 active pharmaceutical licenses worldwide
