ISO 13485 Certification in Singapore

Medical Devices-Quality Management System(MDQMS)

ISO 13485 Certification in Singapore

ISO 13485  is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes. If you looking for ISO 13485 certification in Singapore. We can help you with it.

B4Q is pioneer Company to provide ISO 13485 Certification in Singapore and Tampines, Pasir Ris, Yishun, Choa Chu Kang, Toa Payoh, Bukit Batok, Queenstown, Clementi and other part of Singapore. ISO 13485 Certification in Singapore can help companies to gain quality management system for medical devices. B4Q provide ISO 13485 Certification in Singapore at the Best Price.

We are Best ISO Certification body in Singapore with wide experience.

5 Key Benefits of ISO 13485 Certification in Singapore

#1 Improve the company’s credibility and image.
#2 Improve your process.
#3 Improve decision-making.
#4 Create a culture of continual improvement
#5 Better employee engagement.

ISO 13485:2016 Requirements

Clause 1: Scope– In this clause we need to define our physical or service boundry to implement MDQMS.

Clause 2: Normative References– this section talk about what are normative reference used in this standard. For Example ISO 9000:2015-Fundamentals and vocabulary.

Clause 3: Terms & Definitions-this clause describe about terms and definitions given in ISO 9000:2015.

Clause 4: Quality Management System – This clause talks about general QMS requirements, as well as the documentation requirements of the standard. It includes the requirements for the Quality Manual, Control of Documents, and Control of Records, all of which are required documents in the QMS.

Clause 5: Management Responsibility – The management responsibility requirements cover the need for top management to be instrumental in the implementation and maintenance of the QMS. Along with planning for the QMS, there is a need for top management to be involved in the ongoing review of the system to ensure customer satisfaction and improvement.

Clause 6: Resource Management – The section on management of resources is short, but covers the necessity to control all resources, including human resources, buildings, and infrastructure and the working environment.

Clause 7: Product Realization – The product requirements deal with all aspects of the planning and creation of the product or service. This section includes requirements on planning, product requirements review, design, purchasing, creating the product or service, and controlling the equipment used to monitor and measure the product or service. ISO 13485 allows for requirements in the section to be excluded if they are not applicable to the company (such as a company that does not design products or services).

Clause 8: Measurement, Analysis and Improvement – This last section includes the requirements needed to make sure that you can monitor whether your QMS is functioning well. It includes assessing customer satisfaction, internal audits, monitoring products and processes, dealing with non-conforming product, and corrective and preventive actions. These sections are based on a Plan-Do-Check-Act cycle.

ISO 13485 vs ISO 9001

ISO 13485 is Medical Device-Quality Management System that is completely derived from ISO 9001. So there are some additional requirement other than ISO 9001. Some additional requirement of ISO 13485 is given below.

✓ Documentation requirements for medical device files,
✓ Work environment requirements,
✓ Contamination control requirements,
✓ Production requirements for cleanliness of products,
✓ Production requirements for sterile medical devices, and
✓ Requirements for reporting to regulatory authorities.

The ISO 9001:2015 updates various requirements for identifying the context of the organization, which were not added into the ISO 13485 standard, such as identification of internal and external issues as well as identifying interested parties and their needs and expectations.

Process for ISO Certification in Singapore

iso certification in singapore