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Discover the Scilife Platform

Create your own Life Sciences Software Platform by choosing the right modules to fit your needs. All modules link together to create seamless and efficient workflows. Discover them!

Document Control

Rock Solid Control of Documentation

Our Scilife Document Control module standardizes and sorts your documents, effortlessly.


Print & Reconciliation

Keep track of printouts and stay FDA 21 CFR 11 compliant

Our Print & Reconciliation module logs every print action and tags every printed page with a unique barcode for easy identification and retrieval.



Train fast, train smart.
Keep everyone fully compliant.

Our Trainings module makes creating, and keeping track of employee trainings a breeze, through highly customizable templates.



Unearth valuable talent in your team in a glance

Stay up to date on the evolving skills of each of your employees through our detailed competences matrix and CV management tool built into our Competences module.


Quality Process Designer

Design your perfect workflow

Design very specific and detailed workflows, especially at enterprise level.



Capture and track every issue

Capture and follow up every issue in our Events module. Register deviations, nonconformities, and complaints in a few clicks.




Make Corrective & Preventive Actions manageable again

Map out a CAPA action plan with our intuitive template, set up automated notifications to reach your assigned approvers, program followup notifications, and fast-track CAPAs to closure.


Change Control

Evolution demands change

Our Change Control module lets you create a clear path for the request, approval, and implementation of modifications, empowering your whole company to participate in changes.



Face Audits and Qualifications with confidence

Our Audits module handles all types of audits; including supplier, internal, outgoing, and incoming audits. Whether you’re hosting or performing an audit, our Audit module makes it effortless.


Risk Assessment

Turbocharge your risk management

Link risk assessment to deviations, nonconformities, CAPAs, and audits to keep everything in one place since all modules are seamlessly integrated.



Fail-proof equipment processes

Equipment maintenance and calibration requires careful planning, management, and proof to ensure continued safety and inspection readiness.


Quality by Design

Complex process improvement, simplified

Simplify the path to improving complex processes in your company by having all process-related data and process-improvement iterations in one central location.


Design & Development

Release planned Q3 2022

Our new module lets you manage the whole medical device design & development process from user needs to design verification and validation according to ISO 13485.



Measuring the right metrics fuels growth

Our KPI module provides you with the real-time performance metrics and historic trends you need to know in order to oversee how your company is doing and find actionable areas.



Powerful maintenance of validation documentation

Our Validations module makes managing validation projects a breeze. It automates the linking of items, maximizing efficiency and traceability.