Modern Medical Device Development

Modern Medical Device Development, available at $19.99, has an average rating of 4, with 30 lectures, based on 3 reviews, and has 9 subscribers.

You will learn about Understanding the phases of medical device development Medical device safety and compliance How to train your staff on new medical device Single – use medical device reprocessing Development of medical device policies Medical device regulation act Home medical equipment This course is ideal for individuals who are Nurse, doctors, health workers, health consultants, students, specialist, companies, hospitals, regulatory agencies, governments, insurance companies, general public, business people etc. It is particularly useful for Nurse, doctors, health workers, health consultants, students, specialist, companies, hospitals, regulatory agencies, governments, insurance companies, general public, business people etc.

Enroll now: Modern Medical Device Development

Summary

Title: Modern Medical Device Development

Price: $19.99

Average Rating: 4

Number of Lectures: 30

Number of Published Lectures: 30

Number of Curriculum Items: 30

Number of Published Curriculum Objects: 30

Original Price: $74.99

Quality Status: approved

Status: Live

What You Will Learn

Understanding the phases of medical device development
Medical device safety and compliance
How to train your staff on new medical device
Single – use medical device reprocessing
Development of medical device policies
Medical device regulation act
Home medical equipment

Who Should Attend

Nurse, doctors, health workers, health consultants, students, specialist, companies, hospitals, regulatory agencies, governments, insurance companies, general public, business people etc.

Target Audiences

Nurse, doctors, health workers, health consultants, students, specialist, companies, hospitals, regulatory agencies, governments, insurance companies, general public, business people etc.

The purpose of a medical device is to benefit others and improve the quality of life. However, in order to keep patient and user risk at a minimum, authorities have tightened up regulations over recent years with the hope that manufacturers will build quality in, while taking risk out of a device. The growing complexity of medical devices requires more advance testing and certification to verify safety, performance and compliance to regulatory requirements. To effectively help patients, healthcare products need to be available. However, before these products are sold, they need to demonstrate safety and effectiveness. As the healthcare industry adapts to connected and evolving technologies, safety standards are always being updated. This makes new types of safety testing a must for today’s healthcare products. It is very important to note that medical device manufacturers, developers and standards authors all look at the same safety issues when it comes to patient care, information access, data security, product safety and result reliability.

Regulatory compliance for medical devices is difficult to navigate. Manufacturers, developers and end users often need assistance to stay on top of the latest trends and standards to keep their product compliant. Effective health technology policies address inequality as well as accessibility, affordability and availability of innovation and core medical devices required to target the health needs, particularly those that address the millennium development goals.

Course Curriculum

Chapter 1: Introduction

Lecture 1: Introduction

Lecture 2: What is medical device

Lecture 3: IS0 13485

Lecture 4: What is the medical device development process

Lecture 5: Medical device regulation act

Lecture 6: Standardization and regulatory concerns

Lecture 7: Packaging standards

Lecture 8: Common challenges that prevent medical device from getting onto the market

Lecture 9: Single- use medical devices

Lecture 10: Global medical device nomen clature

Lecture 11: Medical software

Lecture 12: Home medical equipment

Lecture 13: Biomedical engineering

Lecture 14: Health technology

Chapter 2: Understanding 5 Phase Of Medical Device Development

Lecture 1: Phase 1: Initiation,opportunity and risk analysis

Lecture 2: Phase 2: Formulation,concept and feasibility

Lecture 3: Phase 3: Design and development verification and validation

Lecture 4: Phase 4: Final validation and product launch preparation

Lecture 5: Phase 5: Product launch and post market surveillance

Chapter 3: Medical Device Safety And Compliance

Lecture 1: Element for evaluation

Lecture 2: Confidence through compliance

Lecture 3: Compliance and safety solution

Chapter 4: Single Use Medical Device Reprocessing

Lecture 1: Single – use medical device reprocessing

Lecture 2: The single use label

Lecture 3: Safety and efficacy of reprocessed SUDs

Lecture 4: International regulation of single- use medical device reprocessing

Chapter 5: How TO Train Your Staff New Medical Device

Lecture 1: Benefits of medical device training

Lecture 2: What to accomplish in medical staff training sessions

Lecture 3: Set training goals

Chapter 6: Development Of Medical Device Policies

Lecture 1: Development of medical device policies

Instructors

Eric Yeboah
MBA/ PGDip

Rating Distribution

1 stars: 0 votes
2 stars: 1 votes
3 stars: 0 votes
4 stars: 0 votes
5 stars: 2 votes

Frequently Asked Questions

How long do I have access to the course materials?

You can view and review the lecture materials indefinitely, like an on-demand channel.

Can I take my courses with me wherever I go?

Definitely! If you have an internet connection, courses on Udemy are available on any device at any time. If you don’t have an internet connection, some instructors also let their students download course lectures. That’s up to the instructor though, so make sure you get on their good side!

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