User Stats

Total reviews: 4
Level: Guru
Member Since: 23/11/2020

Profile Information

First name Eva
Last name Martin Becerra
I have professional experience in:

Biotech, Clinical trials, Diagnostics, Digital Health, Medical Device, Medicine, Personalised medicine, Business strategy, IP & Licensing, Regulatory, Startups, Technology transfer

Help us confirm that you're an expert

Since 2007 I have been involved in the management of biomedical projects in different development stages.
During this period, I have gained deep knowledge of the technology transfer between public centers and private companies, due diligence and licensing-out processes.

Regarding IP, I established the patentability strategy for the companies’ patents portfolio, oversaw R&D results disclosure and participated in drafting and prosecuting applications.

Regarding regulatory affairs and clinical research, I supervised the mandatory safety preclinical package, carried out the compilation for the investigational medicinal product dossier, participated in the design and execution of phase 0- II clinical trials and in the launching of in vitro diagnosis products, out-licensing and spin-out processes.

In 2013, I founded my own consultancy services company (Kinrel) and since then, I helped TTOs and entrepreneurs to move forward their project along the value chain.

LinkedIn

es.linkedin.com/in/evambkinrel

Base
Name

Eva Martin Becerra

I have professional experience in:

Biotech, Clinical trials, Diagnostics, Digital Health, Medical Device, Medicine, Personalised medicine, Business strategy, IP & Licensing, Regulatory, Startups, Technology transfer

Help us confirm that you're an expert

Since 2007 I have been involved in the management of biomedical projects in different development stages.
During this period, I have gained deep knowledge of the technology transfer between public centers and private companies, due diligence and licensing-out processes.

Regarding IP, I established the patentability strategy for the companies’ patents portfolio, oversaw R&D results disclosure and participated in drafting and prosecuting applications.

Regarding regulatory affairs and clinical research, I supervised the mandatory safety preclinical package, carried out the compilation for the investigational medicinal product dossier, participated in the design and execution of phase 0- II clinical trials and in the launching of in vitro diagnosis products, out-licensing and spin-out processes.

In 2013, I founded my own consultancy services company (Kinrel) and since then, I helped TTOs and entrepreneurs to move forward their project along the value chain.

LinkedIn

es.linkedin.com/in/evambkinrel