BerlinAnalytix — The In-Vivo Company

Research partnerships

Your research.
Our histological expertise.

Specialist processing and analysis, integrated into your study. Working with device developers, CROs and research teams from the first study question to the final evidence.

Discuss a collaboration How we work together
Microscopic image of a bone section with a 20 micrometre scale bar
A closer view of the material.Histology / BerlinAnalytix

01 / Working together

A defined role.
A shared investigation.

Commission the histological work package or involve us in the wider study. The methods, interfaces and deliverables are agreed with your team.

Device & biomaterial developers

Histological evidence for prototype decisions, comparative investigations and later study programmes. Specimen preparation and endpoints are planned around the device and its intended function.

Explore study types

CROs & partner laboratories

Specialist histological processing and analysis within your study. Agree sample handling, sectioning, staining, evaluation and reporting before specimens enter the workflow.

Meet the laboratory

Academic & research teams

Analytical work packages for collaborative research. Study endpoints, methods, quantitative evaluation and publication figures developed around the scientific question.

View published work

02 / Implantation & analysis

Connected expertise.
Defined responsibilities.

Our core is specialist histological processing and analysis. Implantation studies are scoped through our integrated implantation laboratory and GLP partner network, according to the programme.

Early-stage implantation

Our integrated implantation laboratory supports feasibility investigations. Study size, timepoints and comparisons are selected around the development decision.

PoC & feasibility studies

GLP study programmes

Work with our GLP partner network for the implantation phase and wider study requirements. The protocol defines each facility’s responsibilities, quality requirements and reporting contributions.

GLP & regulatory studies

The Berlin laboratory

Preparation. Analysis. Evidence.

Undecalcified hard-tissue and soft-tissue processing, study-specific staining, histopathological assessment and quantitative histomorphometry.

Laboratory & quality scope

03 / Study coordination

From study question
to a defined work package.

Agree the investigation before work begins, with clear handovers between the sponsor, study facilities and analytical team.

  1. Define the evidence

    Device, development stage, endpoints, timepoints and relevant comparisons.

  2. Agree the study

    Protocol, specimens, responsibilities, quality scope and deliverables.

  3. Prepare & investigate

    Processing, staining and analysis matched to the agreed endpoints.

  4. Report the findings

    Traceable observations, quantitative results and study-specific interpretation.

04 / Study pathways

The right study
for the next decision.

Explore the scope, investigations and evidence for each study type.

PoC & feasibility

Early evidence within product development

Research studies

Comparative evidence across timepoints

Material studies

Biomaterial characterisation and processing changes

GLP & regulatory

Documented investigations for submission programmes

Clinical studies

Clinical specimens, efficacy and post-market follow-up

Start a collaboration

Your project.
A clear next step.

Share the device or material, development stage and evidence you need. We’ll define our contribution with your team.

Discuss your project