Driving force in

Drugs and Health Products Development Services

CRO

Fully Integrated Services

Why use VectorB2B

Guidance for biotechs: program design, feasibility, regulatory, QA

Management of development programs: a principle point of contact (project manager) to plan and execute development programs including pre-clinical studies, toxicology, CMC, clinical studies. Providing study oversight for clients.

Expertise: discovery, pre-clinical, CMC, Phase I and subsequent phases

Cost Reduction: Cost effective location without compromising quality

What We Do

We speed up your drug development program via CDMO/CRO integrated services delivered by a team of excellence

Drug Discovery

From target identification to candidate validation

Toxicology

Certified in vitro and in vivo safety studies

Manufacturing Services

From lab scale to GMP manufacturing

Clinical Services

Complete clinical study program development

Integrated Solutions

Full services from the bench to bedside

From Bench 2
Pharma Market

ask an expert

Testimonials

VectorB2B has been our partner since the beggining of the pandemic and we could not be happier with them. Very open, costumer-centered, and always willing to help. The access we have to their services and its quality has saved us time and worries during these difficult times

Dr. António Cruz Ferreira, Desconfinamento360 Client

Working with VectorB2B not only provided us with great data and thorough reports regarding the experiments we requested, but their scientific expertise helped optimize and improve the design of our experiments and success of our project. I definitely recommend engaging VectorB2B

Daniel Emerling, SVP Research, Atreca, Inc.

Case Studies

The Burden of Retinal Degenerative Diseases

In vitro ADME-Tox characterization in drug discovery and development

The endeavor of getting your products into the market from Preclinical to Clinical Studies

News

EATRIS SPOTLIGHT PROGRAMME 2025 – PORTUGAL

VectorB2B, ULS Coimbra and IdiPAZ invite you all to attend the workshop: Transition from Preclinical Research to Clinical Trials Find out here the meeting program and register here

The 1st GLP certified facilities in Portugal

We design and execute your preclinical GLP/ non-GLP toxicology studies…

SPF 2025

Estamos a organizar a sessão científica intitulada “Como podem os CoLABs apoiar os desafios da Saúde Global?” https://lnkd.in/dnDVwafm Juntem-se a nós no próximo dia 4 de Julho, 11h30-13h30 Visitem-nos no nosso stand!