Global Certificate in ISO 13485 and MDR Compliance

Name: Global Certificate in ISO 13485 and MDR Compliance
Availability: InStock

-- ViewingNow

The Global Certificate in ISO 13485 and MDR Compliance course is a comprehensive program that equips learners with the necessary skills to excel in the medical device industry. This course emphasizes the importance of understanding and implementing ISO 13485, a quality management system standard specific to the medical device industry, and the European Medical Device Regulation (MDR).

5,0

Based on 5.674 reviews

2.778+

Students enrolled

GBP £ 140

GBP £ 202

Save 44% with our special offer

Start Now

AboutThisCourse

With the increasing demand for medical devices and the constant evolution of regulatory requirements, this course is essential for professionals seeking career advancement. Learners will gain expertise in critical areas, including risk management, document control, and quality assurance, enhancing their ability to contribute to their organization's success. By earning this globally recognized certificate, learners demonstrate their commitment to quality, compliance, and patient safety.

HundredPercentOnline

LearnFromAnywhere

ShareableCertificate

AddToLinkedIn

TwoMonthsToComplete

AtTwoThreeHoursAWeek

StartAnytime

NoWaitingPeriod

CourseDetails

• Introduction to ISO 13485: Understanding the standard, its purpose, and benefits for medical device organizations
• Key Components of ISO 13485: Quality management system, documentation, management responsibility, resource management, product realization, and measurement, analysis, and improvement
• ISO 13485 vs ISO 9001: Comparing the requirements and differences for medical device organizations and general manufacturing
• Implementing ISO 13485: Steps, tools, and best practices for a successful implementation
• Internal Audit and Management Review: Preparing and conducting internal audits, and management review processes for continuous improvement
• MDR (Medical Device Regulation) Overview: Understanding the new regulation and its impact on medical device organizations
• MDR Compliance and Risk Management: Implementing risk management processes for MDR compliance
• MDR Labeling and Technical Documentation: Requirements and best practices for labeling and technical documentation
• MDR Vigilance and Post-Market Surveillance: Processes for post-market surveillance and vigilance for MDR compliance
• MDR and ISO 13485 Integration: Strategies for integrating MDR requirements into an existing ISO 13485 quality management system.

CareerPath

In the UK medical device industry, staying updated with global certifications like ISO 13485 and MDR compliance is essential for professionals aiming to advance their careers. This 3D pie chart highlights the demand for various roles in the job market, providing valuable insights for those looking to specialise in this field. With a 3D effect and transparent background, this visual representation showcases the: 1. **Quality Manager**: With 25% of the demand, these professionals ensure that medical devices meet the required standards and regulations. 2. **Regulatory Affairs Manager**: Holding 20% of the demand, these experts navigate the complex regulatory landscape for medical devices. 3. **ISO 13485 Consultant**: Representing 15% of the demand, these professionals offer guidance on implementing and maintaining ISO 13485 quality management systems. 4. **MDR Compliance Specialist**: With 10% of the demand, these specialists ensure compliance with the new Medical Device Regulation in the EU. 5. **Clinical Affairs Manager**: Holding 10% of the demand, these professionals manage clinical trials and ensure the safety and efficacy of medical devices. 6. **Biocompatibility Expert**: Representing 10% of the demand, these specialists assess the compatibility of medical devices with living tissue. 7. **Documentation Specialist**: With 5% of the demand, these professionals manage the creation, review, and maintenance of technical documentation. 8. **Training Specialist**: Holding 5% of the demand, these professionals develop and deliver training programs for medical device companies. These roles display the growing need for professionals skilled in ISO 13485 and MDR compliance in the UK medical device industry. By visualizing the job market trends, this 3D pie chart offers a comprehensive understanding of the industry's requirements, enabling professionals to make informed career choices.

EntryRequirements

BasicUnderstandingSubject
ProficiencyEnglish
ComputerInternetAccess
BasicComputerSkills
DedicationCompleteCourse

NoPriorQualifications

CourseStatus

CourseProvidesPractical

NotAccreditedRecognized
NotRegulatedAuthorized
ComplementaryFormalQualifications

ReceiveCertificateCompletion

WhyPeopleChooseUs

LoadingReviews

FrequentlyAskedQuestions

WhatMakesCourseUnique

▼

HowLongCompleteCourse

▼

WhatSupportWillIReceive

▼

IsCertificateRecognized

▼

WhatCareerOpportunities

▼

WhenCanIStartCourse

▼

WhatIsCourseFormat

▼

CourseFee

MostPopular

FastTrack GBP £140

CompleteInOneMonth

AcceleratedLearningPath

ThreeFourHoursPerWeek
EarlyCertificateDelivery
OpenEnrollmentStartAnytime

Start Now

StandardMode GBP £90

CompleteInTwoMonths

FlexibleLearningPace

TwoThreeHoursPerWeek
RegularCertificateDelivery
OpenEnrollmentStartAnytime

Start Now

WhatsIncludedBothPlans

FullCourseAccess
DigitalCertificate
CourseMaterials

AllInclusivePricing

GetCourseInformation

PayAsCompany

RequestInvoiceCompany

PayByInvoice

EarnCareerCertificate

GLOBAL CERTIFICATE IN ISO 13485 AND MDR COMPLIANCE

IsAwardedTo

LearnerName

WhoHasCompletedProgramme

London School of International Business (LSIB)

AwardedOn

05 May 2025

BlockchainId s-1-a-2-m-3-p-4-l-5-e

AddCredentialToProfile