Cellab CDMO

Cellab CDMO is a Contract Development and Manufacturing Organization (CDMO) specialized in cell and gene therapy.

Our team has a decade of expertise in ATMP manufacturing and GMP processes, we specialize in collaborating closely with small teams to advance ATMPs from basic research to early clinical trials.

We partner closely with our clients, acting as an extension of their team to accelerate the journey from bench to bedside. Our agile approach allows us to adapt quickly to evolving project needs, ensuring timely delivery and success.

CMG MedDev

CMG MedDev is a dedicated consulting services wit more than 30 years of experience with focus on the field of medical devices, in vitro diagnostics, CDx, software and AI. We offer a tailor made solutions in Regulatory, Quality and Clinical services. CE mark submissions and FDA pre- submissions & submissions.

Genesis Biomed

GENESIS Biomed is a consultancy firm in the biomedical healthcare sector specialized in providing consulting services in the genesis and first phases of lifecycle of biomedical spin-off and start-up companies, mid and big-size companies, investors, entrepreneurs and research centers.

Based in our expertise we help entrepreneurs and researchers to shape their business plan and we support them in the private fundraising process. We have raised 80 M€ in the last years in 21 rounds.

We are Associate Partner at EIT Health and we are engaged to 24 EU projects with TOP EU institutions: H2020, Horizon Europe, EIT Health and EIT Digital.

Our expertise domains are biopharmaceutical, biotechnological, medical devices, in vitro diagnostic, digital health, artificial intelligence, nutraceutical and cosmetic. With more than 20 years of expertise in the healthcare sector, we are born in May 2017 and we are headquartered in the Barcelona Science Park, and also with company sites in Madrid center and at La Marina in Valencia.

Histocell

Vivotecnia

Vivotecnia is a fully independent European toxicology safety contract research organization (CRO) with headquarters based in Madrid, Spain.

We offer services to support preclinical product development for pharmaceutical and biotech companies

Our laboratories and different units are perfectly equipped and, working under Good Laboratory Practices. Our animal units house rodents, dogs, rabbits, minipigs and nonhuman primates, whose choice is justified by being the best candidates for different types of preclinical studies, thus minimizing the potential risks which might arise in the human species.

Working with Vivotecnia means working with a partner. Our highly qualified study management team, with lengthy experience in both pharmaceutical and CRO industries, fully understands the challenges you face and is committed to providing the knowledge, advice and high-quality service you expect.

We aim to ensure that you achieve your goals despite the magnitude of the challenges you face. Our innovative approach to study design ensures that your study is developed optimally, cost-effectively, ethically and in compliance with regulatory requirements