Year | Name | Fees | Total |
---|---|---|---|
1st Year | Tution Fee | EUR 7980 | 7980.0 |
Starting Date | Application Deadline | Status |
---|---|---|
2022-09-01 00:00:00.000 | 2022-08-15 00:00:00.000 | Active |
2023-01-01 00:00:00.000 | 2022-12-15 00:00:00.000 | Active |
The key points that you should know about your admission process are:
1. Application along with supporting documents will be processed on TEN Agent portal.
2. Student will receive the admission offer either conditional or unconditional on his TEN Agent portal.After accepting the offer Fee invoice will be generated on student account.
3.After getting the fee invoice student can pay the fee and fee receipt can be found on TEN Portal (Ten Agents)
Introduction to the pharmaceutical sector – 3 ECTS
Organization of the health system
Structure and organization of the pharmaceutical industry
Professional skills – 3 ECTS
Job search and career plan
High-impact presentations
Management skills
Research and development of medicines – 7 ECTS
Pharmacology, pharmacogenetics, pharmacogenomics
Design, drug screening and preclinical safety assessment
Pharmaceutical development
Design of clinical trials and observational studies
Statistics applied to clinical research
Clinical trial management – 3 ECTS
Regulation of clinical research and GCP
Roles and responsibilities of promoters and researchers
Research project management
Data management, interpretation and publication of clinical trials
Monitoring of clinical trials – 3 ECTS
Pre-study, initiation, monitoring and closing visits
Researcher meetings
Clinical trial audits and inspections
Registration, pharmacovigilance, pharmacoeconomics – 3 ECTS
Pharmacovigilance and risk management
Procedures for the authorisation of medicinal products
Economic evaluation of medicines
Master's degree final project – 6 ECTS
Design of a clinical trial of an investigationsed drug
Internships – 52 ECTS
Internships in pharmaceutical companies and CROs
Business communication skills (optional) – 3 ECTS
Presentation & Negotiation skills
Reading Documentation & Report Writing
Effective Meetings
In the Master in Monitoring and Management of Clinical Trials you will develop skills such as project organization and management, flexibility and teamwork capacity that will allow you to access positions related to the monitoring and management of different types of clinical studies. Thanks to this, you will be able to integrate into the teams of professionals who work in the research of the medical advances of the future.
Most of the new medicines that are made available to patients are researched and developed by the pharmaceutical industry in a process that is carried out thanks to the coordinated work of large international and multidisciplinary teams. The role of the clinical trial monitor is key for this research to meet the highest standards of quality and safety.
For visa process, refer to this link:
https://india.blsspainvisa.com
The VISA Application should be submitted online with Documents mentioned below.
Study Permit – Checklist of Documents.
Visa Application Form
Covering letter from the applicant with complete summary explaining the purpose of visit
Official invitation (signed & stamped) from Indian company/institute stating the details of course/internship
along with their certificate of registration
Photocopy of PAN card in case of India Company
Official letter (signed & stamped) from Spanish Institute stating the details of the course/internship, location
and that the course/internship is part of the curriculum
Copy of graduate/post-graduate diploma or certificate (must have graduated since 2 years or less).
All Academic Documents
10th Marksheet
12th Marksheet
IELTS/PTE
Health Insurance
TB Certificate(After Medical Doctor will give you this document).
Passport / Old Passport (if any)
2 Photographs with white background. (35mm X 45mm) (80% face should be visible)
Aadhar Card
VFS appointment Letter