Kick off your study in days, not months.

Say goodbye to delays, approvals, and support tickets. ShareCRF gives you the control, speed, and simplicity you always wanted in an EDC.

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They already trust in ShareCRF

The Real Advantages of Using ShareCRF

Fast Study Setups

Launch your clinical study in days—not months. Keep your team moving and your sponsors happy with rapid deployment.

Flexible Mid-Study Changes

Make updates instantly, without coding, tickets, or delays. Adapt your protocol on the fly and keep your study on track.

Reliable, Human Support

Get fast, expert help when you need it. Our support team is responsive, knowledgeable, and truly there for you.

Compliance Built-in

Every study is automatically auditable, validated, and compliant with GCP, 21 CFR Part 11, GDPR, and HIPAA standards.

Success Stories

“ It's a very easy, simple user friendly system, affordable, pricewise and the professional service provided by the support or by the design team is, is amazing”

Sahar Boostenay
Clinical Director at Revamp Medical

"What I like most about ShareCRF is the independence and also the functionalities, which are really sophisticated."

Lenka Styfalova
Clinical Data Manager at Diabeloop

“The designing process is quite easy, and we can customise the form to our needs. And also thinking about the researchers that use this tool, I think for them is very easy. One of the benefits is that it eases the work a lot both for us and for the users.”

Gabriela Jimenez
Medical Doctor at Picterus AS

“I would have used other very large well known systems, but actually, there were just a number of different issues that did not make those systems suitable for the type of CRO that we were trying to run. We were definitely looking for a better system in terms of ease of use, level of customer service and changes and that interaction was very, very important to us and price actually as well”

Nicola Wall
CEO at Afortiori

“If a company is in the need to develop quick collect data forms that comply with regulatory requirements, this is an ideal solution. You can develop complex tools quickly.”

Iker Navarro
CEO at Noorik Biopharmaceuticals

“The major benefit would be time, lots of time saving. It is easy to introduce the data and it's really fast to export the data and from that on to analyse the data obtained in the studies.”

Rita Carilho
Project Manager & Scientific Affairs at AIDFM-CETERA

“The fact that I can design the eCRF by myself, I realised it is really helpful because I can modify all the time, like when I need and I think it is a huge benefit”

Anjali Raja
Co-Founder at Collabree

ShareCRF in numbers

+
6.500
Users
+
750
Studies
+
70
Countries
99.99
%
Availability

“I always received the most professional and immediate response by the customer service team. They offered solutions that I couldn't even think of, which was amazing.”

Sahar Boostenay
Clinical Director at Revamp Medical
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Intuitive and Efficient Interface

Designed for researchers—not programmers. ShareCRF is easy to use, reduces errors, and keeps everyone away from spreadsheets.

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Everything you need, nothing you don't

Visual Study Editor

Easily design clinical eCRF with our drag & drop editor. Without programming.

ePRO

Collect patient data directly from their devices, and integrate it automatically in the EDC along with other clinical data.

Randomization

Flexible, easy, integrated and with support for treatment stock management.

Medical Coding

Code on-the-go using MedDRA and  WHODrug: medical coding integrated with data.

Monitoring

Adapt the data review and verification strategy to the needs of each study.

API

Connects the EDC to other systems via our application programming interface.

Compliance Made Simple

Leverage ShareCRF to meet complex regulatory requirements in the simplest way. Designed to facilitate compliance with legal and regulatory standards. ShareCRF is validated using the GAMP5 methodology.

  • Validated System (GAMP5)
  • 21 CFR Part 11 (FDA)
  • Annex 11: Computerised Systems (EMA)
  • ISO 9001 certified
  • GDPR
  • ICH E6 (R2) - Good Clinical Practice
  • HIPAA
  • ISO 27001 certified
  • GDPR
  • ICH E6 (R2) - Good Clinical Practice
  • HIPAA
  • ISO 27001 certified
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Common Questions

How long does setup really take?

Most studies are ready to collect data within 3-5 days of starting. Simple studies can be set up in hours, while complex multi-arm trials can take one to two weeks.

Do I need technical skills to use ShareCRF?

If you can use Excel, you can use ShareCRF. No coding, SQL, or technical knowledge required. Our visual editor is designed so that you don't have to program a single line of code.

What if I need to change the CRF mid-study?

Make changes yourself, instantly. Add fields, modify validations, or update forms without support tickets. All changes are versioned, tracked, and audit-trail compliant.

Is ShareCRF compliant with regulations?

Yes. ShareCRF is compliant with GCP, 21 CFR Part 11, GDPR, and HIPAA. We provide all validation documentation needed for your regulatory submissions and audits.