Become an expert in Veterinary Clinical Trial Legislation in just a few weeks"

The general and fundamental basis for carrying out projects related to clinical research and being able to place veterinary drugs on the market is the Regulatory Framework and the Legislation applicable in these cases. This is why professionals in this area with in-depth and specialized knowledge, requiring advanced skills, are in high demand.

This is the reason why TECH has designed a Postgraduate certificate in Legislation Applicable to Veterinary Clinical Trial, to provide students with the necessary skills to master this field and to be able to perform their work with the highest quality in the work and handling the rules applicable to each case.

All this, in a comfortable 100% online mode that allows students to organize their schedules and studies as best suits them, without the need to travel and with the possibility of accessing all content from any device with internet connection, whether Tablet, mobile or computer.

A program designed for you, so you can reach your most demanding goals in the legislative field of Veterinary Clinical Trial"

This Postgraduate certificate in Legislation Applicable to VCT contains the most complete and up-to-date educational program on the market. Its most notable features are:

• The development of case studies presented by experts in Legislation Applicable to Veterinary Clinical Trial
• The graphic, schematic, and practical contents with which they are created, provide scientific and practical information on the disciplines that are essential for professional practice
• Practical exercises where self-assessment can be used 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

A program with which you will be able to perfect your skills in Spanish Legislation and Regulations applicable to veterinary medicines and Clinical Trials"

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.

It has the best theoretical and practical material to achieve your most ambitious goals in a few weeks"

Acquire the most up-to-date knowledge about the AEMPS and the EMA"

The structure and content of this program have been designed by the best professionals in the field, who make up TECH's team of experts. All this, through the most efficient pedagogical methodology, Relearning, which guarantees the best possible assimilation of the contents, in a natural, progressive and precise way, avoiding the student to dedicate excessive time to study.

Thanks to Relearning, you will not have to invest extra hours in studying and you will be able to combine it with your other activities or obligations"

Module 1. Legislation Applicable to VCT

1.1. European Medicines Agency (EMA)

1.1.1. Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on Veterinary Medicinal Products
1.1.2. Maximum Residue Limits
1.1.3. Royal Decree 1157/2021, of 28 December, Which Regulates Industrially Manufactured Veterinary Medicinal Products
1.1.4. Royal Decree Regulating the Distribution, Prescription, Dispensation and Use of Medicines (in Draft)

1.2. Animal Welfare
1.3. International Conference on Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products VICH Program
1.4. Registration Procedures for Veterinary Drugs

1.4.1. Centralized, Mutual Recognition and Decentralized Procedure

Opt for a program that will allow you to get up-to-date on the National Antibiotic Resistance Plan"