Training Workshop: Digitalisation of your QMS (Supported by WSG)

Workshop Information

Date: 30 & 31 July 2019 | 9.00am – 5.00pm

Venue: SMF Centre for Corporate Learning (2985 Jalan Bukit Merah, SMF Building, Singapore 159457)

Pricing: Refer to Workshop PDF below


Who should attend?

  • Medical device specification developers and manufacturers (product owners).

  • Medical device contract manufacturers and precision engineering companies that are moving into Medical Technology (medTech) industry.

  • Companies intending to convert from ISO 13485:2003 (lapsed) to ISO 13485:2016.

  • Companies looking to expand globally.

  • Personnel working in the Quality/Regulatory department, or as a Management Representative, or Document Controller.


Why Attend This Workshop?

Supported by Workforce Singapore (WSG), this workshop aims to transform the medTech Industry and raise your company’s productivity through the acquisition and adoption of an EQMS! This is in line with raising awareness of the Industry Transformation Map (ITM) / Lean Enterprise Development (LED) initiatives.

This workshop focuses on providing an overview of the ISO 13485:2016 and how its requirements can be continuously met using an Enterprise Quality Management Software System (EQMS) - Stendard Solution™.

We will share how effective implementation of the standard can help your company fulfill medical device regulatory requirements globally. Theoretical training will be complimented by practical elements, with the use of technological tools.

You will be trained to efficiently manage your documented processes using an EQMS, to enhance your business productivity, achieve audit readiness and have effective supervision of your quality management processes. Should fresh documents be required, you will be digitally equipped to produce your customised set of documents that is line with the ISO 13485:2016 requirements.


Join us!

You will better understand how the implementation of an EQMS can allow you to raise productivity, streamline and effectively manage your business processes digitally, and continuously meet ISO 13485:2016 requirements.

We look forward to seeing you!

 

Organised by:

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Supported by:

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For More Information:

Download the PDF attached for more information on the workshop timetable, pricing and trainers’ profiles.

 

Any other questions? Contact us!