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Quality Platform for Contract Research / Manufacturing Organizations (CRO / CMO)

Accelerate efficiency and
meet your trial deadlines

Avoid delays and extra bureaucracy by improving transparency and sponsor collaboration

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illustration of a hand holding a star to represent how Scilife helps Medical Devices companies to put quality at the center

Get your trials fully compliant

Implement a smart quality software solution and follow all the regulatory requirements—controlling your documents' lifecycle, conducting internal audits, and tracking employees' expertise.

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Don’t be a burden: enhance efficiency and transparency

Clinical research is often perceived as costly and time-consuming. Invest in a smart QMS solution and improve data quality, patient safety, and access to clinical trial processes.

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Become more efficient and meet all your project deadlines

Manage workload, timelines, and resources wisely using a smart quality tool that helps you improve performance.

Where All Your Quality Comes Together

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Popular Features

Documents
& Records


Knowledge

Processes with configurable workflows

Advanced Analytics

Other features

  • Electronic Signatures (21CFR11 compliant)
  • Full validation documentation package (GAMP5)
  • Audit Trail
  • User tasks list
  • Personalized training
  • 1 : 1 Technical Support

How we support other companies like yours

We are QA’s performance-boosting allies

Picture of Sarah Vanrenterghem, head of Quality at Novitan, a happy Scilife customer
novitan

"Scilife offers all the required functionalities in a flexible, cloud-based package which complies with the GxP guidelines."

Sarah Vanrenterghem
Head of Quality at Novitan
Pendulum pills in pink background to illustrate the quote of their Director of Quality and Regulatory as satisfied customer of the quality software for pharma and Biotech, Scilife
Pendulum logo as customer of Scilife

"We have been using Scilife to monitor the quality metric KPI's closely. It has enabled us to narrow down the root causes for several deviations with an ultimate benefit of improving quality and reducing costs."

Achal Deo
Director of Quality and Regulatory at Pendulum
Picture of Cyrille Drouot, Quality and Chemistry Manufacture Control Director at Genoscience Pharma, a happy Scilife customer
Genoscience Pharma logo, as Scilife's CRO / CMO customer

"The ISO9001:2015 certification is a key demonstration of a fully integrated quality approach which reinforces the efficiency and robustness of our development programs. We achieved such a key objective with the help of Scilife."

Cyrille Drouot
Quality and Chemistry Manufacture Control Director at Genoscience Pharma

Struggling to improve efficiency
and meet research deadlines?

Let's chat to find a solution that suits your needs!
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Best Pharma and Biotech Software on G2

Customers rated Scilife the Best Pharma and Biotech Software again in the G2 Summer 2022 report.

This ranking system considers both user satisfaction and market presence of the software, compared to similar products, placing Scilife as the leader in the Pharma & Biotech category.

Scilife badge to communicate that remains Leader in the Pharma & Biotech Software Category in G2 summer 2022 report
Scilife badge to illustrate that Scilife wins 'Best Relationship' with buyers
G2 Summer Report Grid where Scilife is rated as the best Pharma and Biotech Software
Illustration of 3 hands creating a fask shape to encourage Pharma & Biotech industry companies to get in touch with Scilife
Illustration of 2 hands building a SaaS interface to encourage Medical Devices & IVD companies to request Scilife's price.
Illustration of a rocket-microscope taking off to encourage Medical Devices companies to book a Scilife demo.