Course in registration of medicines and regulatory affairs (university degree with 5 ECTS credits)

The pharmaceutical industry is one of the sectors with the highest figures in billing and generation of direct and indirect wealth, being key in the maintenance of the welfare state. The medications are subjected to numerous exhaustive studies before being marketed. Therefore, it is essential to know all the aspects related to the current regulations that the drug registration must comply with, to achieve the authorization of its commercialization. For this, the personnel of the Department of Registries or Regulatory Affairs must possess the appropriate technical and scientific knowledge to manage to launch medications to the market guaranteeing their quality and safety. This course in the Registry of Medicines and Regulatory Affairs will form you in it.

- Provide information on the pharmaceutical dispensation service. - Know the different phases that comprise the process of registration of medicines nationwide. - Deepen the role of drug marketing within the pharmaceutical market. - Understand the procedures for the authorization and supervision of medicines.

This course in the Registry of Medicines and Regulatory Affairs encourages your incorporation into one of the most out -of -level markets both nationally and internationally. You will get the knowledge you need to maximize your professional capacities in all those areas of both theoretical and practices related to the departments of Regulatory Affairs of the pharmaceutical companies.

This course in the Registry of Medicines and Regulatory Affairs will provide you with a complete vision of the environment that surrounds the registration and regulation of medicines, specializing in functions related to registration and commercialization, information, scientific communication and medical information. You can be part of the Sector of the Record Departments / Regulatory Affairs that has a very low level of unemployment.

The course in the Registry of Medicines and Regulatory Affairs is aimed at professionals from areas of health and related sciences and to all those interested in acquiring knowledge related to the registration and commercialization of pharmaceutical products. You will acquire a specialization to work in the regulatory department of any pharmaceutical company.

This training is not included in the scope of official regulated training (Infant Education, Primary Education, Secondary Education, Official Professional Training FP, Baccalaureate, University Degree, Official University Master and PhD). It is therefore a complementary and/or specialization training, aimed at acquiring certain skills, skills or aptitudes of a professional nature, being able to be barely as merit in workbags and/or opposition competitions, always within the complementary training section and/or continuous training being always essential to review the specific requirements of the public labor stock of the public labor stock market.