We design the protocol with the definition of the objectives, the study design and the methodology that will guide it (determination of the sample and statistical hypothesis, statistical model and so on. This phase also includes the organization and monitorization of the trial in a way that will permit its control throughout the process, assuring the success.

Accuracy and precision are our essential requirements during the field study with animals and the management of the product. In our approach for the reduction of mistakes, we monitor the tests ensuring that the protocol is being followed and the data is adequately collected, assuring its reliability and traceability.

We implement the GCP (Good Clinical Practice), international regulations for the ethic and scientific quality applied in the field of trials with living beings. Its objective is the quality increase in both healthcare and clinical research, being a safeguard of the animal rights, security, and welfare protection.

Our clients have the complete knowledge of the ongoing process and our team is always willing to listen new needs or requirements.

The data management process is the basis of the decision-making and on which the conclusions of the trials are supported, so we are fully involved in its correct execution.

Each project has its own document for the data collection so that we will acquire the information needed.  These files are design so that they will give us efficiency when transferring the information from the original document to the database. Being clear, time saving.

We fully exploit and analyze the data with RStudio, professional software for data science teams with a powerful programming language. T&T applies the highest quality methodologies, such as Lean Management, Six Sigma and SPC (Statistical Process Control).

We use double data entry tables (or contingency tables) that show all the necessary statistical information from the experiments. Furthermore, we validate data through query resolution so that shared data is accurate and consistent.

The entire statistical analysis plan and the results obtained are collected in the final report that we present to the client. This document is adapted so that it is clear and concise, but with all the necessary information detailed.

From transparency, we show the methods used, results obtained and their interpretation and discussion from the clinical point of view. We treat the data with the utmost confidentiality, protecting our clients and taking the necessary measures during its handling. We sign confidentiality agreements both internally and with the entities from the beginning of the contractual relationships and we are proud to say that all our clients are completely satisfied with the discretion with which we act.