CRO & preclinical consultant solutions I Versa Biomedical

Where innovative biomedical solutions prepare to win in the market.

The Versa Surgical Centre is a state-of-the-art surgical facility designed for the global medical device and pharma industry.

We give your teams, your surgeons and your KOLs the environment they need to train, validate and launch. From sales force training to live product demos, from human factor studies to content creation. Everything happens here, under one roof, in complete confidentiality.

Your whole journey, in one place.

From first model to market-ready — with the access, privacy and speed your team needs at every stage.

From early design to real-world adoption

From proprietary animal models and GLP-certified preclinical studies to surgical training and product launch readiness: we are built to take you further, faster.
Europe's most accessible surgical training hub

4 minutes from Barcelona Airport. Your teams fly in and fly out. Hotels 300m away. Private gardens for networking and catering.
No constraints. 100% confidential

Your IP, your device, your strategy — protected. Separate areas for each client. 24/7, 365 days a year. No overlap, no leaks.

Who we work with

Built for the teams that bring medical innovation to market.

Medical Device Companies

You're launching a new device and need surgeons trained before market entry. Real hands-on sessions, live demos, and content for your sales team. We run it all, from session logistics to video production.

Pharma & Biotech

You need human factor and usability data for your regulatory submission, or a controlled environment to validate how your product performs in a real clinical setting. We provide the facility, the models and the documentation.

Everything your solutions need. Under one roof.

Product launches, sales training, KOL programmes, human factor studies and content creation, all run by the same team, on the same site.

No coordinating between vendors, no handoffs between facilities. From your first live demo to the final piece of content, everything moves together, so your device gets to market without losing momentum.

01

Product Launch & Live Demos

Showcase your device to surgeons and KOLs in a real OR. Live video streaming, recording and debriefing support.
02

Sales Force & Distributor Training

Get your commercial teams hands-on before they face a customer. Surgical training on porcine, human cadavers or dry lab, with clinical support throughout.
03

KOL Engagement Programmes

Build relationships with the surgeons who matter. Invite KOLs to your own dedicated facility.
04

Human Factor & Usability Studies

Generate the usability evidence your regulatory file needs. Documentation aligned with FDA and EU MDR requirements.
05

Content Creation

Capture your device in action. Video, photo, clinical education content produced in a real OR, with real surgeons.

Specialized capabilities and infrastructure for every phase of your project.

Real operating rooms, real capacity, minutes from the airport.

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operating rooms
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meeting rooms
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from BCN Airport

Space & Equipment

Everything set up and ready before you arrive.

5 fully equipped ORs

Dry lab, porcine model and human cadaver

Live video streaming and recording

Location & Flexibility

Fly in, walk in, get started.

4 min from Barcelona Airport (4.6 km)

300m from 4★ hotel

Private networking gardens

24/7, 365 days

Closed-door, confidential

Full Support

Every detail handled, so you can focus on the session.

Content production

Event & catering support

On-site coordination

Custom branding

The credentials that guarantee your study stands up.

Versa Biomedical is a fully GLP-certified CRO, compliant with the guidelines issued by the relevant health authorities. Every session at our Surgical Center operates under the same quality standards as our preclinical testing — so your documentation is always submission-ready.

A quality system that applies to non-clinical studies that assess the safety and efficacy of chemicals, medical devices and pharmaceuticals to be used on man, animals or in the environment.

ISO 13485 specifies for Medical Devices the requirements of a quality management system when an organization manages products and services that meet customer requirements and applicable regulations.

We have joined the agreement on Openness on Animal Research promoted from the Federation of Scientific Societies in Spain (COSCE) and the European Association of Research Animals (EARA).

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