Quality Assurance System

Quality Assuance Made Digitally

The Most Amazing QA Software

With this software any lab can now get the Feburay 17025 Accreditaion they deserve to make their lab stand out from all the rest. Anyone in the lab can now become a QA.

Get access to the best Quality Assurance module in any Laboratory Information Management System!

Resource Requirements

With this section Personnel, Equipment and many more other things can be mannaged

Process Requiremtns

In this section Contacts, Complaints and many more gets controlled from here

Management Requirements

In this section you can now upload your Corrective Actions, Risk and Oppertunities and much more.

Signatory Management

Digital Signatures for signatories can be uploaded into this section and can be checked if needed


8 October 2021

TOPIC: ISO/IEC 17020:2012 – Clause 8 Management system requirements: Clause 8.8 Preventive actions.

TIME: 8 October 2021, 10:00 – 12:00

DESCRIPTION: The MiChem team will discuss the available approaches to successfully implement the management system requirements as set out in ISO/IEC 17020 for Preventive actions.

Further to this, pointers will be provided to assist you in finding risks associated with different implementation practises and share some thoughts around what you could potentially expect during an audit.

NOTE: You will be given the opportunity to ask questions and clarify specific concerns with regards to topic presented.

  1. Follow this link to pre-register for the free webinar – 8 October 2021
  2. After registering, you will receive a confirmation email containing information about joining the webinar

PRESENTER: Santie van Niekerk


5 November 2021

TOPIC: Performing an internal audit on ISO/IEC 17025:2017 Clause 8.8 Internal audits and Clause 8.9 Management reviews.

TIME: 5 November 2021, 10:00 – 12:00

DESCRIPTION: The purpose of Internal auditing is to verify compliance of the laboratory’s quality management system to ISO/IEC 17025 and additional requirements, as well as to ensure the system is effectively implemented and maintained. The MiChem team will clarify the various aspects (compliance and implementation) that laboratories should audit to ensure compliance to ISO/IEC 17025:2017 Clause 8.8 and 8.9.

NOTE: You will be given the opportunity to ask questions and clarify specific concerns with regards to topic presented.

PRESENTER: Santie van Niekerk


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