WEBINARS

INDUSTRY (LABORATORY) DEVELOPMENT AND CONTINUOUS COMPLIANCE

Is keeping up with the changes of ISO/IEC 17025:2017 an uphill battle for your laboratory? Do you find it difficult to obtain the relevant information, struggling with the interpretation of the standard and accreditation criteria?

If the answer is YES, then this is the right platform to help you and your team, understand.

MiChem Dynamics has years of experience and will be able to walk you through the process. An “industry-first” platform to support your laboratory, ensuring information and ideas are shared, allowing for full compliance to ISO/IEC 17025:2017 and guide you through the additional accreditation requirements.

The best of all – this is FREE!

Disclaimer:
Only participants who attend the live webinar session, will receive the presentation, certificate and additional supporting documents presented. The webinar platform gives us detailed information as to which participants attended the webinar live as well as the duration of attendance. Watching the recorded version does not qualify for the issuing of the certificate or the sharing of the presentation and additional supporting documents. The recorded version of the webinar is for insight only.

WEBINAR REGISTRATION 7 FEBRUARY 2020

TOPIC: ISO/IEC 17025:2017 – Clause 4 General requirements: 4.1 Impartiality, 4.2 Confidentiality and Clause 5 Structural requirements

TIME: 7 February 2020, 10:00 – 12:00

DESCRIPTION: The MiChem team will discuss the available approaches to successfully implement the general requirements set out in ISO/IEC 17025 for impartiality, confidentiality and structural requirements.
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 – 22 November 2019:
2. After registering, you will receive a confirmation email containing information about joining the webinar.

PRE – REGISTER

WEBINAR REGISTRATION 13 March 2020

Topic:ISO/IEC 17025:2017 – Clause 6 Resource requirements: 6.2 Personnel, 6.3 Facilities and environmental conditions, 6.4 Equipment, 6.5 Metrological traceability and 6.6 Externally provided products and services

Time: 13 March 2020, 10h00-12h00 (GMT+2)

DESCRIPTION: The MiChem team will discuss the available approaches to successfully implement the resource requirements set out in ISO/IEC 17025 for personnel, facilities and environmental conditions, equipment, metrological traceability and externally provided products and services.

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.

PRESENTER: Santie van Niekerk

PRE – REGISTER

Speaker – Santie van Niekerk

Co-Founder & Director @MiChem Dynamics
After spending 12 years in the medical, food and environmental industry, Santie had a clear vision of what services should be provided to address the opportunities in the industry. She is a qualified microbiologist, ISO/IEC 17025 facilitator, auditor and management system expert with practical experience in industry trends and compliance

WEBINARS 2020

Friday: 10 April 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 7 Process requirements: 7.1 Review of requests, tenders and contracts, 7.2 Selection, verification and validation of methods, 7.3 Sampling and 7.6 Evaluation of measurement uncertainty

Friday: 8 May 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 7 Process requirements: 7.4 Handling of test or calibration items, 7.5 Technical records and 7.7 Ensuring the validity of results

Friday: 19 June 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 7 Process requirements: 7.8 Reporting of results, 7.9 Complaints, 7.10 Nonconforming work and 7.11 Control of data and information management

Friday: 10 July 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 8 Management requirements: 8.1 Options and 8.2 Management system documentation

Friday: 14 August 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 8 Management requirements: 8.3 Control of management system documents and 8.4 Control of records

Friday: 25 September 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 8 Management requirements: 8.5 Actions to address risks and opportunities and 8.6 Improvement

Friday: 23 October 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 8 Management requirements: 8.7 Corrective actions and 8.8 Internal audits

Friday: 13 November 2020
Time: 10h00-12h00 (GMT+2)
Topic: ISO/IEC 17025:2017 – Clause 8 Management requirements: 8.9 Management review

Should you need more information around any of these topics NOW, or would like to recommend additional topics please feel free to contact Santie van Niekerk on santie@michemdynamics.co.za or +27 82 770 7127