Become an expert in all areas of Veterinary Clinical Trials in a few months and without leaving home"

The Design, Management and Treatment of a Clinical Trial are fundamental to guarantee the validity of the results, which will later be used as scientific evidence for decision making. Experts in this area require specific and very complete knowledge to be able to carry out their work with maximum efficiency, which is why there is an increasing demand in the labor market.

For this reason, TECH has created a Postgraduate diploma in Veterinary Clinical Trial Design, Management and Processing, with which to enhance the knowledge and expand the skills of students in this area, so that they can stand out in their work in this area. For this purpose, the syllabus addresses topics such as Technical Documentation, Individual Selection, Contract Management, Certification, Evaluation and Specialized Methodology in Clinical Trials, among others. 
All this, under a 100% online modality that gives comfort and freedom to students to organize their schedules and studies in the way that best suits them. In addition, with total availability of completely up-to-date theoretical and practical content, as well as the possibility of opening the materials from any device with an Internet connection, whether it is a tablet, computer or cell phone. 

Enjoy all the content from your computer, tablet or cell phone"

This Postgraduate diploma in Veterinary Clinical Trial Design, Management and Processing contains the most complete and up-to-date scientific program on the market. Its most notable features are:

• The development of case studies presented by experts in Veterinary Clinical Trial Design, Management and Treatment
• The graphic, schematic and eminently practical contents of the book provide scientific and practical information on those disciplines that are essential for professional practice
• Practical exercises where the self-assessment process can be carried out to improve learning
• Its special emphasis on innovative methodologies
• 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

Test your new skills in Clinical Trials, with the most complete and dynamic practical activities"

The program’s teaching staff includes professionals from the field who contribute their work experience to this educational program, as well as renowned specialists from leading societies and prestigious universities. 

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 education programmed to learn 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 during the educational year. For this purpose, the students will be assisted by an innovative interactive video system created by renowned and experienced experts.

Delves into a wealth of material on Incorrect Documentation and Specialized Methodology"

Acquire new knowledge in risk assessment and field work"

TECH has selected the most distinguished experts in Clinical Trials to bring their experience and specialized knowledge to the syllabus, resulting in a complete and up-to-date program that represents a unique opportunity in the academic market. Moreover, always based on the most efficient pedagogical methodology, Relearning, in which TECH is a pioneer and which guarantees the natural and progressive assimilation of the essential concepts by the students.

TECH Relearning guarantees optimal assimilation of essential concepts, without the need to dedicate excessive time to study" 

Module 1. The Veterinary Clinical Trial I. Design and Methodology

1.1. Veterinary Clinical Trials

1.1.1. Veterinary Clinical Trial Research
1.1.2. Conditions for Conducting a Veterinary Clinical Trial Investigation
1.1.3. Types of Veterinary Clinical Trials

1.1.3.1. Types of Trials According to the Study Design
1.1.3.2. Parallelisms
1.1.3.3. Crusader
1.1.3.4. In Pairs
1.1.3.5. Sequentials

1.2. Data Collection Notebooks

1.3. Identification of Information Sources for a Veterinary Clinical Trial

1.3.1. How To Find Information We Are Interested In

1.3.1.1. Choice of Source
1.3.1.2. Resources and Access Modes
1.3.1.3. How to Search for the Best Evidence on a Topic

1.4. Elaboration of a Protocol for the Conduct of a Clinical Trial with Veterinary Medication

1.4.1. General Information
1.4.2. Justification and Objectives
1.4.3. Test Outline

1.5. Design of the Veterinary Clinical Trials

1.5.1. Individual Selection
1.5.2. Inclusion/Exclusion Criteria
1.5.3. Treatment
1.5.4. Destination of Study Animals, Products Derived from Study Animals and Products under Clinical Investigation and Control Products
1.5.5. Adverse Events (AEs)

1.6. Methodology in Veterinary Clinical Trial Research

1.6.1. Hypotheses
1.6.2. Randomization
1.6.3. City
1.6.4. Sampling
1.6.5. Uncontrolled Trials
1.6.6. Controlled Trials

1.6.6.1. Open
1.6.6.2. Blind
1.6.6.3. Double-Blind
1.6.6.4. Triple-Blind
1.6.6.5. Pilot

1.7. Methodological Procedures in a Veterinary Clinical Trial (VCT)

1.7.1. Discrimination Between CD in Humans and Animals
1.7.2. Differences
1.7.3. Implementation
1.7.4. External and Internal Validity
1.7.5. Variables
1.7.6. Consent
1.7.7. Reproducibility
1.7.8. Risk

1.8. Evaluation of the Efficiency of the Veterinary Clinical Trial.

1.8.1. Statistics
1.8.2. Records Management
1.8.3. Annexes Attached to Protocol
1.8.4. Changes in Protocol
1.8.5. References

1.9. Research Quality in a Veterinary Clinical Trial

1.9.1. Legal Aspects
1.9.2. Scientific Aspects
1.9.3. Risk-Benefit Assessment

1.10. Ethical Principles in a Veterinary Clinical Trial

1.10.1. Historical Background
1.10.2. Ethical Codes
1.10.3. Application of Ethical Principles

Module 2. The Veterinary Clinical Trials II. Management, Start-ups and Commissioning

2.1. Clinical Trial Management Preclinical Development

2.1.1. Preclinical Development

2.1.1.1. Animal Experimentation Committees

2.1.2. Exploratory Clinical Trial
2.1.3. Regulatory Clinical Trial

2.2. Clinical Trial Authorization Process

2.2.1. Application for a Product in Veterinary Research
2.2.2. Request for a Veterinary Clinical Trial

2.3. Documents at the Beginning of the Clinical Trial

2.3.1. Contract Management
2.3.2. Clinical Trial Protocol
2.3.3. Informed Consent

2.4. Clinical Trial Initiation and Start-Up

2.4.1. Initial Visit and Center Opening
2.4.2. Data Collection Notebooks (DCNs)
2.4.3. Electronic Data Collection (EDC)

2.5. Documentary Archive of a Clinical Trial

2.5.1. Medication Shipment and Management
2.5.2. Documentation Custody

2.6. Final Report

2.6.1. Center Closures
2.6.2. Clinical Trial Documentation Audit
2.6.3. Audit of Data Management Activities

2.7. Laboratory Certification

2.7.1. Laboratory Certification: GMP
2.7.2. Laboratory Certification: GLP
2.7.3. Laboratory Certification: ISO

2.8. Regulatory Dossier Structure

2.8.1. Document Management
2.8.2. Validation of the Internal Structure
2.8.3. Electronic Communication with Regulatory Agencies

2.9. Writing Results

2.9.1. Publication of Clinical Trials in Scientific Journals

2.10. CONSORT Recommendations

Module 3. The Veterinary Clinical Trials III. Trial Treatment

3.1. Description of Trail Treatment

3.1.1. What Does the Dose Description, Interval, Route and Form of Administration and Duration of the Treatment to be Trialed Depend on?
3.1.2. Criteria for the Creation of Patterns Throughout the Trial

3.2. Application of Special Rules to the Trail Treatment

3.2.1. Situations for Application of Special Rules to Trail Treatment
3.2.2. Measures to Assess Therapeutic Compliance in Special Situations

3.2.2.1. Examples of Special Situations

3.3. Treatment Response

3.3.1. Data Collection

3.4. Methods and Evaluation of Treatment Response

3.4.1. Description of the Methods Used for Response Assessment and Quality Control

3.4.1.1. Complementary Tests: Laboratory Tests, Diagnostic Imaging, Electrocardiogram, etc.

3.4.2. Evaluation of Data Obtained as a Function of Response

3.5. Monitoring. Trial Treatment Plan

3.5.1. Monitoring Plan
3.5.2. Research Timeline
3.5.3. Types of Schedules

3.6. Main Problems in the Methodological Approaches to Treatment in the Trial

3.6.1. Incorrect Documentation
3.6.2. Samples

3.6.2.1. Missing Samples
3.6.2.2. Delayed Samples
3.6.2.3. Forgotten Parameters
3.6.2.4. Incorrect Sampling Times
3.6.2.5. Laboratory Kit Problems

3.7. Specialized Methodology in Treatment I

3.7.1. Clinical Trials in Veterinary Oncology

3.7.1.1. Trail Phases
3.7.1.2. Therapeutic Targets
3.7.1.3. Biological Samples
3.7.1.4. Bioequivalence

3.8. Specialized Methodology in Treatment II

3.8.1. Clinical Trials in Veterinary Infectious Pathology I

3.8.1.1. Analysis Objectives
3.8.1.2. Epidemiological Clinical Trials Methodology

3.9. Specialized Methodology in Treatment III

3.9.1. Clinical Trials in Veterinary Infectious Pathology. Prevention and Control of Veterinary Infectious Pathology II

3.9.1.1. Prevention and Control of the Disease

3.9.1.1.1. Institutional Strategies

3.9.1.2. Risk Assessment

3.10. Specialized Methodology in Treatment IV

3.10.1. Clinical Trials in Veterinary Neurology

3.10.1.1. Neurology Research

3.10.1.1.1. Research Areas

3.10.1.2. Field Work
3.10.1.3. Interpreting Results

Enroll now and get a professional position in one of the most promising areas in the veterinary field"