MiChem Dynamics offers its renowned services globally, ensuring quality everywhere.
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ISO/IEC 17025 accreditation is the hallmark of credibility in testing and calibration. At MiChem Dynamics, we bring unparalleled expertise and a meticulous approach to help your laboratory achieve and maintain this prestigious accreditation. Our seasoned consultants understand the intricacies of compliance and strive to fine-tune every aspect of your processes to meet these rigorous standards.
We’re passionate about quality. Our ISO/IEC 17025 consulting services are designed to not only meet but exceed international standards, providing you with the assurance of top-tier quality in every test and/or calibration. From method validation to equipment calibration and personnel training, we’re dedicated to elevating your laboratory’s capabilities to meet and exceed ISO/IEC 17025 requirements.
Our clients include, but are not limited to, various types of calibration, microbiology, chemistry, physical, pharmaceutical, forensic toxicology, and water testing laboratories.
MiChem Dynamics is based in South Africa, with footprint in and outside the African continent. Our main focus to implement effective and efficient laboratory management systems to ensure accuracy and reliability of results.
Join forces with us and unlock the full potential of your laboratory. Let’s embark on a journey where accuracy is not just a goal but a perfected reality. Your laboratory’s pursuit of excellence starts right here.
ANNA MOYO
~ Marketing and Business Development Manager
+27 74 779 5239 | anna@michemdynamics.com
ANGELINE NEL
~ Business & Training Manager
+27 78 335 0528 | angeline@michemdynamics.com
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Starting-up or expanding a laboratory is a major, challenging and often times complicated task.
Whether you are building a new laboratory, or expanding your current one, we can assist with determining the financial resources required to achieve your objectives.
Furthermore, we are able to determine the continuous running costs of the laboratory which considers the direct and indirect expenses related to day-to-day operations.
Do you need to document a Quality Management System (QMS) that is compliant to ISO/IEC 17025:2017, relevant regulatory and/or accreditation requirements?
Our extensive services include taking this task off your hands whereby we develop a fully documented QMS which is tailored to your specific laboratory, environment, and processes.
Furthermore, we provide training on the new QMS and manage the implementation process in a structured manner to ensure that you successfully achieve your objectives.
Are you struggling as a Quality Manager to keep up with the activities related to implementing and maintaining your Quality Management System? Or do you rather need someone to take ownership of the quality management role in your laboratory?
We offer an extensive quality assurance retainer service which is tailored to your requirements and managed by our experienced team to ensure you achieve your ongoing quality objectives.
Do you know the actual number of employees that are required to successfully run your laboratory?
We can assist with determining the minimum number of personnel required for each department’s day-to-day functions by taking into consideration all task-based activities, the time required to effectively complete them, as well as consider the non-operational activities which also use personnel time.
By determining the minimum personnel resources that are required to effectively run your laboratory, you can improve the facility’s operations management as well as be in a better position to motivate for changes with top management.
Are you struggling to effectively document a Quality Management System (QMS) that is compliant to ISO/IEC 17025:2017 and accreditation requirements? Or are you rather looking for some fresh ideas as a means of improvement in your QMS?
We have developed an extensive database of document templates to assist laboratories with successfully implementing their quality-related requirements.
A Quality Management System (QMS) consists of an extensive list of documents which are required to be reviewed at set intervals to ensure that ISO/IEC 17025:2017, regulatory and/or accreditation requirements have been fulfilled, and that the current practices and processes in your laboratory are reflected in the QMS.
Whether you require a single document or the full QMS to be reviewed, we can assist with this process to ensure you remain compliant to the relevant requirements.
Do you have a new method which needs to be validated or verified in your laboratory? Or does your current method need to be reverified and you are struggling to find the time and resources required to successfully complete this on time?
Whether you need a method to be developed, validated, or verified, we can assist by fully managing the practical aspect ourselves in your laboratory, as well as ensure the proper documenting of the results and compiling the final reports.
Do you find that a particular process or workflow is not efficient in your laboratory? Is there a particular aspect of your day-to-day operations that you want to optimise?
Using our extensive hands-on and practical experience in the laboratory industry, we can assist by identifying the bottlenecks and improving your processes and/or workflows to ultimately achieve an efficient and optimised working environment.