All equipment information on a single screen.

Tracking everything that happens to the device.

Add photos of the device and attach all documents.

Add technical staff reports for external maintenance.

Check all records of the device to find out what, when and by whom (internal maintenance, failures, etc.).

Creation and follow-up of Non-Conformities (NC) and Proposal for Improvement.

Configurable “security” levels.

What were the causes and how is it going to be solved?

Analyse and Evaluate the problem to ensure that it does not recur.

Check what, when and by whom an action was performed.

Attach files to the NCs.

Calendar events will appear at each step.

The workflow provides the requirements of ISO 15189 to keep issues under control.

List of all tests that are configured in the laboratory.

See the test requirements and which device performs the test.

Ensure that each test has its documentation completed.

Within each test you can find all related information: section, report section, units, method, collection instructions, storage instructions, sample type, sample treatment and graphs related to internal quality control.

Create different calendars for different needs.

Configure as many as you want.

Link them to employees.

Assign each type of event a different colour to make it easily identifiable.

Mark events as done and filter out those that are still to be done.

Fully integrated with the other modules: no matter where the tasks are performed, they will be reflected in the calendar!

Updated profiles for each employee.

All employee data in one place: contact information, unit, working life, work experience…

Calendar view to quickly see what tasks remain to be done.

Advanced system for applying ratings and approving what an employee is authorised to do.

Define a metric to measure: reports, samples …

Select how often you want the system to check this metric.

Check back frequently to see how these metrics are evolving and make business decisions based on real data!

Create an audit with all the information you need.

Each audit will have as many criteria and activities as it wishes.

For each activity to be audited:

• Write a full report on this.

• Give it a numerical value as a rating.

• Add any comments.

Evaluate the audit and see what the outcome was.

Report it in PDF.

Create Non-conformities or Proposals for Improvement from the audit review.

Define all programmes and check that the laboratory will participate for part of the year.

Schedule the dates by which the samples must arrive at the laboratory and the deadline for reporting the result and display them in the Calendar.

Evaluate all results with customised rules to accept/reject results.

Automatically create non-conformities if results need to be reviewed.

Attach the supplier’s reports to keep everything organised.

Easily see how that test is performing over time and take steps (if necessary) to improve it.