Quality Assurance System

Quality Assurance Made Digitally

The Most Amazing QA Software

With this software any lab can now get the ISO/IEC 17025 Accreditation they deserve to make their lab stand out from all the rest. 

LABMIN also provides qualified personnel to assist with the initial LIMS QA setup of your laboratory’s unique processes, so that your lab can experience a seamless transition to a stress-free accreditation process.

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

Resource Requirements

In this section your laboratory Equipment, Personnel and other resources can be managed

Process Requirements

Keep valid record of your contracts and complaints as well as overall quality control with this section.

Management Requirements

Here you can manage all Risks, Non-conformances, Corrective actions and Improvements that were logged and much more

Signatory Management

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

Webinars

25 November 2022

TOPIC: ISO 15189:2012 – Clause 5 Technical requirements: Clause 5.8 Reporting of results, Clause 5.9 Release of results & Clause 5.10 Laboratory information management.

TIME: 25 November 2022, 10:00 – 12:00

DESCRIPTION: ISO 15189:2012 Medical laboratories – Requirements for quality and competence. The MiChem team will discuss and explain the requirements of ISO 15189 Clause 5.8 Reporting of results, Clause 5.9 Release of results & Clause 5.10 Laboratory information management. Attending this webinar will support your medical laboratory towards compliance of these requirements.

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 –25 November 2022
  2. After registering, you will receive a confirmation email containing information about joining the webinar

PRESENTER: Santie van Niekerk & Vinay Moodley

PRE-REGISTER Now

 

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

PRE-REGISTER Now

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

PRE-REGISTER Now

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