Regulatory Aspects of Clinical Trials Course + 8 ECTS Credits

Online Training

Regulatory Aspects of Clinical Trials Course + 8 ECTS Credits

Name: Regulatory Aspects of Clinical Trials Course + 8 ECTS Credits en Italia
Brand: INESALUD
SKU: 341422-2501
Availability: InStock

icon-image--AbjlOSDZzVEJNY0s3S__icon_7yVPEV

200 hours

icon-image--AcnI1bkFZTjZZaTE3U__icon_xJgfxr

8 ECTS

icon-image--AWUI0N2tWMzVrNzMzT__icon_DgE8xz

Spanish

Knowing the regulatory aspects of clinical trials is essential to ensure that regulatory standards are met in all phases of drug development. In clinical trials there are interests from both the pharmaceutical industry and researchers, which increases the importance of adequate management to avoid any irregularity. By completing this Course on Regulatory Aspects of Clinical Trials you will be able to apply your knowledge, not only in the legislative area, but also in deontological matters, pharmacovigilance, marketing and other aspects of drug development. Complement your training with INESEM, differentiating yourself from other professionals in your sector.

Instituciones educativas

260€

Request information

I'm interested I'm interested

I'm interested

Details to take into account

icon-image--AUzhDQ3dCN3hXZ1RaS__icon_p9pcRc

Multilingual support

icon-image--AQVZldVUybkd2c2xSS__icon_ptJqNh

Digital certificate included

icon-image--AV0haRDQrMjBZRURoV__icon_zyt3R8

Assistant Phia

Objectives

- Learn the registrations and authorizations necessary for clinical trials and the marketing of health products. - Recognize the ethical and legal foundations of the clinical trial. - Know the role of marketing in the economic system and its current trends in the world of health. - Inform about pharmaceutical marketing and its different policies

Content

Career opportunities

Develop your professional career in the field of clinical trials. This course encourages your incorporation into one of the markets with the most opportunities within the pharmaceutical industry. You will gain the knowledge you need to manage the regulatory aspects of clinical trials. Complement your training, differentiating yourself from other professionals in your sector.

What it prepares you for

With this course you will learn about the regulatory aspects of clinical trials, which will allow you to access positions in the pharmaceutical industry related to the legislative aspects of different types of clinical studies. Develop yourself as a professional within a multidisciplinary and growing team within the pharmaceutical industry and contribute to the scientific advances of the future.

This course is aimed at anyone interested in being part of the clinical trials environment, as well as lawyers, pharmacists or other health professionals, such as doctors, biologists and veterinarians, who wish to continue training and/or want to make their way in the world of the pharmaceutical industry.

Our training is 100% online, which allows students to self-regulate their study and adapt it to their own needs. We are committed to personalized and autonomous teaching, with an approach based on critical thinking and constructivism.

We have a highly specialized teaching team that will accompany you throughout the entire teaching-learning process. This will allow you to personalize your training even more, since we adapt to your pace and needs.

You will have access to our learning platform, MyLXP, from any device and at any time of the day, allowing you to decide how and when to study. All of this is possible thanks to our Educa LXP (Learning Experience Platform) methodology, an environment designed to boost your educational progress, encourage innovation and offer a personalized learning experience adapted to each need.