Cellab CDMO

how-we-work

About

CGT CDMO

Welcome to Cellab CDMO, your dedicated partner in advancing cell and gene therapy solutions. As an End-to-End Contract Development and Manufacturing Organization (CDMO), we specialize in supporting therapy developers advance their Advanced Therapy Medicinal Product (ATMP) development from concept and early-stage through to clinical programs and commercialization.

At Cellab, our mission is to accelerate your ATMP development from bench to bedside. We are committed to delivering excellence in every aspect of our work to ensure rigorous adherence to quality standards and regulatory requirements under GMP. With our agile approach, we can swiftly adapt to your evolving needs of your product to guarantee timely delivery and success.

Explore how you can realize the full potential of your ATMP by partnering with Cellab.

From bench to bedside

As and End-to-End provider, we guide your project from initial research to commercialization with tailored solutions that are designed to fit your specific needs. Spanning from R&D to Clinical Development, our team navigates your ATMP from its current state to your envisioned future set-up to align with your needs and objectives within a structured timeline.
diagrama cellab

How we work

We make it easy

Cellab CDMO provides top-tier collaboration services, guaranteeing GMP compliance across the entire drug development.

By working closely with our clients and adopting a flexible and collaborative approach, we ensure a successful and less risky outcome for your ATMP development project.

Why choose Cellab CDMO?

CLIENT-CENTRIC

We integrate seamlessly with your team, acting as an extension of your organization. Our personalized approach ensures alignment with your project goals, timelines and specific requirements.

GMP & REGULATORY EXPERTISE

With a deep understanding of GMP requirements and regulatory standards, we navigate your project and its complexities efficiently to ensure your project meets regulatory expectations.

COST-EFFECTIVENESS

By maintaining a lean organizational structure and efficient processes, we are able to offer competitive pricing without compromising on quality thereby making advanced therapies more accessible.

END-TO-END SERVICE

From sourcing biological starting material to EU batch release, we offer comprehensive services including process development, GMP manufacturing, QC, Fill & Finish and storage to ensure continuity and quality throughout your product lifecycle.

Services

Tailored made services

We offer a broad range of services, tailored made and highly adaptable to the clients need. It includes bioprocess scaling design from R&D to GMP, ATMP manufacturing, GMP batch release, GMP storage area, among others.

Manufacturing, Science, and Technologies (MS&T)

▪️ Transition from Early-stage. developments to GMP manufacturing.
▪️ Hands-on partnership, working closely with your team.
▪️ A full team for skilled aseptic operators with years of expertise in biologic manufacturing.

GMP and GMP-Like Manufacturing

▪️ Cell Therapy.
▪️ Gene Therapy.
▪️ Aseptic Fill&Finish.

Quality Control and characterization

▪️ Flow cytometry.
▪️ Cell counter and viability.
▪️ Endotoxin Ph. Eur. 2.6.14.
▪️ Sterility tests – Ph.Eur.2.6.1 & Ph.Eur.2.6.27.
▪️ Mycoplasma test Ph. Eur 2.6.7.
▪️ Potency assays

GMP storage area

▪️ RT: 20-25ºC.
▪️ Refrigeration: 2-8ºC.
▪️ Freeze and ultra-freeze: -20ºC and -80ºC.
▪️ Cryopreserved: -150ºC.

Logistic assistance, including Import/Export

▪️ UE batch release.
▪️ Regulatory assistance.
▪️ Global transportation and brokerage capabilities.

Facilities

Facilities designed for your projects:

Our state-of-the-art facilities are designed to advance cell therapy solutions. To ensure precision and scalability, all rooms are fully equipped with best-in-class equipment for GMP manufacturing of autologous & allogenic cell therapies.

From early-stage development to GMP manufacturing, our facilities operate in strict adherence to global regulatory requirements and provide adaptable space to meet your specific project needs for consistent & safe ATMP production.

MS&T Laboratory
Clean Room B
Cryogenic area
QC laboratory
Flow cytometry
Clean Room B
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Team

Who we are

Our team of experienced and enthusiastic professionals bring a deep understanding of GMP requirements, regulatory standards, and industry best practices to every project we undertake. Discover more about this dynamic group who are poised to facilitate the journey of your therapy.
Alex Marfany

Alexandre Marfany Pluchart

Chief Executive Officer
Alex joined Cellab as CEO in 2020 and leads our team with strong focus on strategic growth and innovation. He holds a BSc in Business Administration and brings over 5 years of experience in managing different companies to his leadership role.
Alba Casamayor

Alba Casamayor Genescà, PhD

Chief Operating Officer & Head of QC
Alba has been an integral part of Cellab since 2013, serving as COO and Head of QC. She oversees our operations with a focus on maintaining high-quality standards. She has over 15 years of experience in both ATMP research & manufacturing under GMP along with managing QC, cells and tissue banks accordance with AABB standards and holds a BSc in Biotechnology, MSc in Advanced Biotechnology and a PhD in Biotechnology.
JUAN JESÚS BANDERA

Juan Jesús
Bandera

Chief Business Officers
Juan Jesús joined Cellab in 2024 as Chief Business Officer driving our strategic initiatives and business development efforts. He holds a BSc in Economy, MSc in Health Economics & Health Care Business Administration. With 20 years of leadership experience in health research management at GM/C-suite level, Juan Jesús has extensive expertise in early-stage clinical trials with ATMPs & managing manufacturing sites.
Raquel Calderon

Raquel Calderon Almendro, PhD

Chief Quality & Compliance Officer
Raquel joined Cellab in 2021 and as Chief Quality and Compliance Officer, she plays a pivotal role in ensuring our products meet regulatory standards and quality requirements. Raquel has over 10 years of experience in the pharmaceutical industry, including positions as QA and QP under GMP and holds a BSc in Pharmacy, an MSc in Pharmaceutical Industry and a PhD in Biomedical Chemistry
Clara Boces

Clara Boces Pascual, PhD

Chief R&D integration and GMP Development
Clara joined Cellab in 2020 as Chief of R&D Integration and GMP Development leading our efforts in integrating R&D strategies with GMP standards. She holds a BSc in Biology, MSc in Biomedicine and a PhD in Biomedicine and has over 10 years of dedicated experience in R&D within Biomedicine focusing on Process Development of GMP Biological Therapies.

Claudia Pujol Bonaparte

Chief Manufacturing Officer & Head of Production
Claudia joined Cellab in 2016 as Chief Manufacturing Officer and Head of Production overseeing all aspects of manufacturing operations with a focus on efficiency and quality. She holds a BSc in Chemistry and an MSc in Pharmaceutical Industry and has more than 10 years of experience in managing biological bank samples under AABB standards, as well as processing and manufacturing ATMPs under GMP regulations.
Joan Muro

Joan Muro De Sas

Chief Marketing Officer
Joan joined Cellab in 2017 as Chief Marketing Officer spearheading our marketing strategies with a focus on increasing brand visibility. He holds a BSc in Journalism and an MBA from ESADE. With over 10 years of experience in Sales and Marketing, Joan brings valuable expertise in developing and executing effective marketing campaigns.

Paul Starz

Business Developer
Paul joined Cellab in 2024 as Business Developer and is dedicated to expanding our business opportunities and driving growth. He holds a BSc in Chemistry & Biochemistry and an MSc in Biochemistry with Major in Biomedicine. With 5 years of experience in both research and business development, Paul bridges the gap between science and business to advance novel ATMPs towards commercialization.

Join us

Be part of a team of experts dedicated to ATMPs. Know the vacant positions and send your application!

Contact

Let’s talk!

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