The current importance of pharmacological research makes this postgraduate diploma an essential training for professionals in the sector"

Increased investment in research in the healthcare field to improve the quality of life of patients means that more and more professionals specialized in this field are needed. Hence the importance of broadening specialization in all research areas.

In this way, students will delve into the study of preclinical drug research, i.e., from the discovery of a molecule with therapeutic activity until it is marketed. Another very important part of this process is to know how to communicate new discoveries, which will allow further research in this field and promote its use. 

Additionally, the essential concepts to support the methodological and semantic complexity of clinical trials are addressed. As such, the categories according to which clinical trials are classified are established in order to delve into different types of clinical trials, such as Phase I trials, due to their great complexity, and post-marketing research of investigational products, due to their enormous involvement in pharmacovigilance processes. 

It should be noted that, within the clinical trial process, the figure of the pharmacists is of great importance, since they perform a series of essential tasks and responsibilities that guarantee the quality of the investigational drug samples.

All of the above makes this postgraduate diploma one of the most up to date and complete programs on the market, and offers the healthcare professional a general overview of clinical trials, but with special and particular cases in which these investigations have proved to be extremely important and beneficial. 

Expand your knowledge through this postgraduate diploma in Clinical Trials that will allow you to specialize until you achieve excellence in this field”

This postgraduate diploma in Clinical Trials contains the most complete and up to date scientific program on the market. The most important features include: 

• The development of case studies presented by experts in Clinical Trials
• The graphic, schematic, and practical contents with which they are created, provide scientific and practical information on the disciplines that are essential for professional development
• New developments in Clinical Trials.
• Practical exercises where the self assessment process can be carried out to improve learning
• Special emphasis on innovative methodologies in Clinical Trials
• Theoretical lessons, questions to the expert, debate forums on controversial topics, and individual reflection assignments
• Content that is accessible from any fixed or portable device with an internet connection

This postgraduate diploma is the best investment you can make when selecting a refresher program, for two reasons: in addition to updating your knowledge in Clinical Trials, you will obtain a qualification endorsed by TECH Technological University”

Its teaching staff includes professionals belonging to the healthcare field, who bring to this program the experience of their work, as well as renowned specialists from prestigious universities and reference societies.

The multimedia content, developed with the latest educational technology, will provide the professional with situated and contextual learning, i.e., a simulated environment that will provide immersive learning programmed to train in real situations.

This program is designed around Problem Based Learning, whereby the professional must try to solve the different professional practice situations that arise throughout the scientific program. For this purpose, the professor will be assisted by an innovative interactive video system created by renowned and experienced experts in the field of Clinical Trials. 

Do not hesitate to take this program with us. You will find the best teaching material with virtual lessons"

This 100% online postgraduate diploma will allow you to balance your studies with your professional work while expanding your knowledge in this field"

The postgraduate diploma in Clinical Trials is aimed at facilitating the performance of the research professional with the latest advances in the sector.  

Thanks to this postgraduate diploma you will be able to specialize in Clinical Trials and learn about the latest advances in the field”

General Objectives

• Establish the phases involved in the development of a new drug
• Analyze the steps prior to the development of a clinical trial (preclinical research)
• Examine how a drug is introduced into the market after the clinical trial has been conducted
• Establish the basic structure of a clinical trial
• Justify the difference between different types of clinical trials
• Compile the essential documents and procedures within a clinical trial
• Develop the clinical trial drug circuit from the point of view of the Pharmacy Service
• Analyze a clinical trial in the setting of a Urology Department
• Establish the specific characteristics of clinical trials in children and adolescents

Specific Objectives

Module 1. Drug research and development

• Explain the pharmacokinetic processes that a drug undergoes in the organism
• Identify the legislation that regulates each of the steps in the development and authorization of a drug
• Define the specific regulation of some drugs (biosimilars, advanced therapies)
• Define the use in special situations and their types
• Examine the process of financing a drug
• Specify strategies for the dissemination of research results
• Present how to read scientific information critically
• Compile sources of information on drugs and their types

Module 2. Clinical Trials (I)

• Establish the types of clinical trials and standards of good clinical practice
• Specify the processes of authorization and distinction of drugs and medical devices in research
• Analyze the evolutionary process of drug research development
• Specify strategies for developing a safety surveillance plan for marketed drugs
• Substantiate the necessary requirements for the initiation of research with drugs in humans
• Establish the elements of a clinical trial research protocol
• Substantiate the difference between inferiority and non-inferiority clinical trials
• Compile the essential documents and procedures within a clinical trial
• Specify the utility and learn the use of data collection notebooks (DCNs)
• Analyze the variety of avenues for the development and funding of non-commercial research
• Disclose the types of fraud committed in clinical trials research

Module 3. Clinical Trials (II)

• Specify the different activities related to sample management (reception, dispensing, custody, etc.) in which the Pharmacy team is involved
• Establish the procedures and techniques involved in the safe handling of samples during their preparation
• Analyze the development of a clinical trial through the vision and participation of the hospital pharmacist
• Compile the specific characteristics of clinical trials in children and adolescents from a legal point of view
• Detail informed consent
• Know the physiological differences between children and adults

An intensive program that will allow you to become a specialist in Clinical Trials in a short period of time and with the greatest flexibility"