Certificate in ISO 13485: Essential Skills

Name: Certificate in ISO 13485: Essential Skills
Availability: InStock

-- viewing now

The Certificate in ISO 13485: Essential Skills course is a professional development program designed to equip learners with the necessary skills to implement and manage quality management systems in the medical device industry. This course is of utmost importance due to the increasing demand for compliance with ISO 13485 standards, which are essential for organizations involved in the design, production, installation, and servicing of medical devices.

4.5

Based on 6,363 reviews

5,820+

Students enrolled

GBP £ 140

GBP £ 202

Save 44% with our special offer

Start Now

About this course

By enrolling in this course, learners will gain a comprehensive understanding of the ISO 13485 standard, its implementation, and its benefits. The course covers key topics such as risk management, document control, and quality management system audits. With this knowledge, learners will be able to ensure their organization's compliance with regulatory requirements, reduce quality costs, and improve overall performance. This course is highly relevant for quality management professionals, medical device manufacturers, and regulatory affairs specialists seeking to enhance their skillset and advance their careers. The certificate in ISO 13485: Essential Skills is a valuable addition to any resume and demonstrates a commitment to professional development in the medical device industry.

100% online

Learn from anywhere

Shareable certificate

Add to your LinkedIn profile

2 months to complete

at 2-3 hours a week

Start anytime

No waiting period

Course Details

• Understanding ISO 13485: This unit will cover the basics of ISO 13485, its purpose, and how it applies to medical device quality management systems. • QMS Documentation: This unit will cover the documentation requirements for a QMS under ISO 13485, including the creation and maintenance of quality manuals, procedures, work instructions, and records. • Management Responsibility: This unit will cover the responsibilities of top management under ISO 13485, including the establishment of quality policy and objectives, management review, and resource management. • Resource Management: This unit will cover the resource management requirements of ISO 13485, including human resources, infrastructure, and the work environment. • Product Realization: This unit will cover the product realization requirements of ISO 13485, including design and development, purchasing, production, and installation. • Measurement, Analysis, and Improvement: This unit will cover the measurement, analysis, and improvement requirements of ISO 13485, including monitoring and measurement, internal audits, and corrective and preventive action. • Medical Device Regulations: This unit will cover the relevant medical device regulations that apply to a QMS under ISO 13485. • Risk Management: This unit will cover the risk management requirements of ISO 13485 and how to integrate risk management into a QMS. • Supplier Management: This unit will cover the supplier management requirements of ISO 13485, including the selection, evaluation, and monitoring of suppliers. • Training and Competence: This unit will cover the training and competence requirements of ISO 13485, including the identification and documentation of training needs, training records, and competence assessment.

Career Path

The ISO 13485 certificate program equips professionals with essential skills in quality management, document control, risk management, regulatory compliance, and supply chain management for the medical device industry. This 3D pie chart highlights the relevance of these skills in the UK job market, providing valuable insights for career development and industry growth. The chart showcases the importance of quality management (45%), document control (30%), and risk management (20%) skills in the medical device industry. The high demand for regulatory compliance (15%) skills emphasizes the significance of adhering to industry standards and guidelines. Supply chain management (25%) skills have a notable presence, indicating the need for professionals to effectively manage supply chain processes in the sector. By understanding these trends, professionals can make informed decisions on enhancing their skill sets to better align with industry demands. This 3D pie chart, with its transparent background and responsive design, offers a compelling visual representation of critical skills and job market trends for those pursuing a career in the medical device industry with an ISO 13485 certificate.

Entry Requirements

Basic understanding of the subject matter
Proficiency in English language
Computer and internet access
Basic computer skills
Dedication to complete the course

No prior formal qualifications required. Course designed for accessibility.

Course Status

This course provides practical knowledge and skills for professional development. It is:

Not accredited by a recognized body
Not regulated by an authorized institution
Complementary to formal qualifications

You'll receive a certificate of completion upon successfully finishing the course.

Why people choose us for their career

Loading reviews...

Frequently Asked Questions

What makes this course unique compared to others?

▼

How long does it take to complete the course?

▼

What support will I receive during the course?

▼

Is the certificate recognized internationally?

▼

What career opportunities will this course open up?

▼

When can I start the course?

▼

What is the course format and learning approach?

▼

Course fee

Get course information

Pay as a company

Request an invoice for your company to pay for this course.

Pay by Invoice

Earn a career certificate

CERTIFICATE IN ISO 13485: ESSENTIAL SKILLS

is awarded to

Learner Name

who has completed a programme at

London School of International Business (LSIB)

Awarded on

05 May 2025

Blockchain Id: s-1-a-2-m-3-p-4-l-5-e

Add this credential to your LinkedIn profile, resume, or CV. Share it on social media and in your performance review.