Regulatory aspects course Clinical trials: regulatory aspects of clinical trials (university degree + 8 ECTS credits)
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Syllabus
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Summary
Knowing the regulatory aspects of clinical trials is essential to ensure that normative standards are met in all phases of medication development. In clinical trials there are interests of both the pharmaceutical and researchers industry, which increases the importance of adequate management to avoid any irregularity. With the realization of this course in regulatory aspects of clinical trials you will be able to apply your knowledge, not only in the legislative area, but in deontological, pharmacovigilance, marketing and other aspects of medication development. Complement your training with Inesem, differentiating yourself from other professionals in your sector.
Goals
Professional opportunities
To prepare you
With this course you will know the regulatory aspects of clinical trials, which will allow you to access positions of the pharmaceutical industry related to the legislative aspects of the different types of clinical studies. Draw yourself as a professional within a multidisciplinary and growing team within the pharmaceutical industry and contributes to the scientific advances of the future.
Who is it addressed to?
This course is addressed to anyone interested in being part of the environment of clinical trials, as well as lawyers, pharmacists or other professionals in the area of health, such as doctors, biologists and veterinarians, who wish to continue training and/or want to make their way to the world of pharmaceutical industry.
Official Character
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.
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Certification
Own Title of Permanent Training Course in regulatory aspects of the clinical trials issued by the European University Miguel de Cervantes accredited with 8 university credits
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