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Regulatory Aspects of Clinical Trials Course + 8 ECTS Credits

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

$303.00

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Duration

200 hours

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Credits

8 ECTS

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Language

Spanish

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No limit

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Agenda

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Credit your success

At the end of the course, you will obtain the accredited qualification

This is not just about learning, but also about accrediting your knowledge with the most important institutions in the sector:

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Qualification Course on Regulatory Aspects of Clinical Trials with 200 hours and 8 ECTS issued by UTAMED-Atlantic Mediterranean Technological University.

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Graduate in Pharmacy. He has a Master's Degree in Teacher Training. She has more than 15 years of experience as an associate pharmacist, developing her work in a pharmacy office and in pharmaceutical care. He has complemented his career with numerous continuing training courses in dermatology, pharmacology, pathologies, cosmetics and teaching. In addition, she has experience as a teacher in intermediate and higher level health training cycles, especially in the Pharmacy and Parapharmacy cycle, as well as in master's programs linked to clinical trials, the pharmaceutical industry and dermopharmacy.

Teaching experience:

Teacher in intermediate and higher level healthcare training cycles: Teaching in the Pharmacy and Parapharmacy cycle. Teacher in master's programs: Master in Clinical Trial Monitoring and Pharmaceutical Development; Master in Pharmaceutical Industry; Master in MSL; Master in Cosmetics and Dermopharmacy.

Professional experience:

Associate pharmacist: Pharmaceutical care in a pharmacy office; Advice on pharmacology and dermopharmacy; Management and dispensing of medications.

Professional skills:

Pharmaceutical care in a pharmacy office; Dermopharmacy and cosmetics; Monitoring of clinical trials; Pharmaceutical industry and pharmaceutical development; Teaching in health training.

Languages:

English B2.

Graduate in Pharmacy. He has a Master's Degree in Teacher Training. She has more than 15 years of experience as an associate pharmacist, developing her work in a pharmacy office and in pharmaceutical care. He has complemented his career with numerous continuing training courses in dermatology, pharmacology, pathologies, cosmetics and teaching. In addition, she has experience as a teacher in intermediate and higher level health training cycles, especially in the Pharmacy and Parapharmacy cycle, as well as in master's programs linked to clinical trials, the pharmaceutical industry and dermopharmacy.

Teaching experience:

Teacher in intermediate and higher level healthcare training cycles: Teaching in the Pharmacy and Parapharmacy cycle. Teacher in master's programs: Master in Clinical Trial Monitoring and Pharmaceutical Development; Master in Pharmaceutical Industry; Master in MSL; Master in Cosmetics and Dermopharmacy.

Professional experience:

Associate pharmacist: Pharmaceutical care in a pharmacy office; Advice on pharmacology and dermopharmacy; Management and dispensing of medications.

Professional skills:

Pharmaceutical care in a pharmacy office; Dermopharmacy and cosmetics; Monitoring of clinical trials; Pharmaceutical industry and pharmaceutical development; Teaching in health training.

Languages:

English B2.

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Course information

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Course information

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.

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.

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.

- 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

Regulatory Aspects of Clinical Trials Course + 8 ECTS Credits

$303.00

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Regulatory Aspects of Clinical Trials Course + 8 ECTS Credits

Agenda

At the end of the course, you will obtain the accredited qualification

Learn from the best in your sector

Course information

Course information

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