FDA compliant medical device development and manufacturing

FDA compliant medical device development and manufacturing, available at $19.99, with 6 lectures, 20 quizzes, and has 1 subscribers.

You will learn about OVERVIEW OF 'HOW TO DEVELOP (FROM CONCEPT ALL THE WAY TO COMMERCIAL SHIPMENT) MEDICAL DEVICES AND MANUFATURE IN COMPLIANCE WITH FDA & INTERNATIONAL REGULATIONS' UNDERSTADING OF FDA'S ONLINE ALL AVAILABLE GUIDELINE PUBLICATIONS & UPDATES RELATED TO MEDICAL DEVICE REGULATORY COMPLIANCE AND APPROVALS AND RELATED TOPICS DEVICE DESIGN VERIFICATION & VALIDATIONS, DESIGN PROCESS, MFG. PROCESS V & V, QUALITY, DOCUMENTATION, SUPPLY CHAIN CONTROLS & OTHER REGULATORY REQUIREMENTS HOW TO UNDERSTAND & MANEUVER USA FDA WEBSITE & SEVERAL HYPERLINKS RELATED TO DEVICE DEVELOPMENT DESIGN, MFG. PROCESS & QUALITY & OTHER REGULATION REQUIREMENTS 1. FDA DEVICE CLASSIFICATIONS CLASS I, CLASS II AND CLASS III ………. 2. FDA AUDITS AND WHAT ARE 483 NOTIFICATIONS ……… 3. FDA RECALL CIRCUMSTANCES FINALLY, REQUIRED ORGANIZATIONAL STRUCTURE AND PERSONNEL REGULATORY TRAINING REQUIRED TO RUN A MEDICAL DEVICE COMPANY. This course is ideal for individuals who are MEDICAL DEVICE INDUSTRY FORTUNE 500 AND STARTUP COMPANIES AND THEIR R & D ENGINEERING, MANUFACTURING ENGINEERING & OPERATIONS & QUALITY ENGINEERING AND DEPARTMENT EMPLOYEES, MEDICAL DEVICE DEVELOPMENT ENTREPRENUERS, MEDICAL UNIVERSITIES AND THEIR STAFF AND STUDENTS, ENGINEERING UNIVERSITIES – COLLEGES STAFF & BIOMEDICAL ENGINEERING STUDENTS & OTHER ENGINEERING DESCIPLINES or DOCTORS, NURSES, HOSPITAL STAFF, HEALTHCARE INDUSTRY PERSONNEL WITH DESIRE TO UNDERSTAND HOW MEDICAL DEVICES ARE DEVELOPMED AND MANUFACTURED IN COMPLIANCE WITH THE FDA & INT'L REGULATIONS INCLUDING SAFETY & EFFICACY or ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY'S MANAGEMENT & EXECUTIVE STAFF or ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY STAFF IN ALL DEPARTMENTS, INCLUDING ASSEMBLY OPERATORS & JANITORS. PERSONNEL WHO NEED HELP TO BE TRAINEED BY DEPARTMENT MANAGEMENT IN CONJUNCTION WITH QUALITY DEPARTMENT or MEDICAL DEVICE COMPANY'S CONSULTANTS AND SUPPLY CHAIN PERSONNEL WITH ALL ABOVE DESCIPLINES or MEDICAL DEVICE INDUSTRY VENTURE CAPITALISTS & INVESTORS WITH A NEED TO UNDERSTAND MEDICAL DEVICE DEVELOPMENT PROCESS OVERVIEW AND REQUIRED INFRASTRUCTURE or ALSO, DESIGN, SUSTAINING, MANUFACTURING , QUALITY ENGINEERS AND OTHER DEPARTMENTAL STAFF FROM OTHER INDUSTRIES WHO HAVE DESIRE TO WORK IN MEDICAL DEVICE INDUTRY. It is particularly useful for MEDICAL DEVICE INDUSTRY FORTUNE 500 AND STARTUP COMPANIES AND THEIR R & D ENGINEERING, MANUFACTURING ENGINEERING & OPERATIONS & QUALITY ENGINEERING AND DEPARTMENT EMPLOYEES, MEDICAL DEVICE DEVELOPMENT ENTREPRENUERS, MEDICAL UNIVERSITIES AND THEIR STAFF AND STUDENTS, ENGINEERING UNIVERSITIES – COLLEGES STAFF & BIOMEDICAL ENGINEERING STUDENTS & OTHER ENGINEERING DESCIPLINES or DOCTORS, NURSES, HOSPITAL STAFF, HEALTHCARE INDUSTRY PERSONNEL WITH DESIRE TO UNDERSTAND HOW MEDICAL DEVICES ARE DEVELOPMED AND MANUFACTURED IN COMPLIANCE WITH THE FDA & INT'L REGULATIONS INCLUDING SAFETY & EFFICACY or ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY'S MANAGEMENT & EXECUTIVE STAFF or ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY STAFF IN ALL DEPARTMENTS, INCLUDING ASSEMBLY OPERATORS & JANITORS. PERSONNEL WHO NEED HELP TO BE TRAINEED BY DEPARTMENT MANAGEMENT IN CONJUNCTION WITH QUALITY DEPARTMENT or MEDICAL DEVICE COMPANY'S CONSULTANTS AND SUPPLY CHAIN PERSONNEL WITH ALL ABOVE DESCIPLINES or MEDICAL DEVICE INDUSTRY VENTURE CAPITALISTS & INVESTORS WITH A NEED TO UNDERSTAND MEDICAL DEVICE DEVELOPMENT PROCESS OVERVIEW AND REQUIRED INFRASTRUCTURE or ALSO, DESIGN, SUSTAINING, MANUFACTURING , QUALITY ENGINEERS AND OTHER DEPARTMENTAL STAFF FROM OTHER INDUSTRIES WHO HAVE DESIRE TO WORK IN MEDICAL DEVICE INDUTRY.

Enroll now: FDA compliant medical device development and manufacturing

Summary

Title: FDA compliant medical device development and manufacturing

Price: $19.99

Number of Lectures: 6

Number of Quizzes: 20

Number of Published Lectures: 6

Number of Published Quizzes: 20

Number of Curriculum Items: 26

Number of Published Curriculum Objects: 26

Original Price: $59.99

Quality Status: approved

Status: Live

What You Will Learn

• OVERVIEW OF 'HOW TO DEVELOP (FROM CONCEPT ALL THE WAY TO COMMERCIAL SHIPMENT) MEDICAL DEVICES AND MANUFATURE IN COMPLIANCE WITH FDA & INTERNATIONAL REGULATIONS'
• UNDERSTADING OF FDA'S ONLINE ALL AVAILABLE GUIDELINE PUBLICATIONS & UPDATES RELATED TO MEDICAL DEVICE REGULATORY COMPLIANCE AND APPROVALS AND RELATED TOPICS
• DEVICE DESIGN VERIFICATION & VALIDATIONS, DESIGN PROCESS, MFG. PROCESS V & V, QUALITY, DOCUMENTATION, SUPPLY CHAIN CONTROLS & OTHER REGULATORY REQUIREMENTS
• HOW TO UNDERSTAND & MANEUVER USA FDA WEBSITE & SEVERAL HYPERLINKS RELATED TO DEVICE DEVELOPMENT DESIGN, MFG. PROCESS & QUALITY & OTHER REGULATION REQUIREMENTS
• 1. FDA DEVICE CLASSIFICATIONS CLASS I, CLASS II AND CLASS III ………. 2. FDA AUDITS AND WHAT ARE 483 NOTIFICATIONS ……… 3. FDA RECALL CIRCUMSTANCES
• FINALLY, REQUIRED ORGANIZATIONAL STRUCTURE AND PERSONNEL REGULATORY TRAINING REQUIRED TO RUN A MEDICAL DEVICE COMPANY.

Who Should Attend

• MEDICAL DEVICE INDUSTRY FORTUNE 500 AND STARTUP COMPANIES AND THEIR R & D ENGINEERING, MANUFACTURING ENGINEERING & OPERATIONS & QUALITY ENGINEERING AND DEPARTMENT EMPLOYEES, MEDICAL DEVICE DEVELOPMENT ENTREPRENUERS, MEDICAL UNIVERSITIES AND THEIR STAFF AND STUDENTS, ENGINEERING UNIVERSITIES – COLLEGES STAFF & BIOMEDICAL ENGINEERING STUDENTS & OTHER ENGINEERING DESCIPLINES
• DOCTORS, NURSES, HOSPITAL STAFF, HEALTHCARE INDUSTRY PERSONNEL WITH DESIRE TO UNDERSTAND HOW MEDICAL DEVICES ARE DEVELOPMED AND MANUFACTURED IN COMPLIANCE WITH THE FDA & INT'L REGULATIONS INCLUDING SAFETY & EFFICACY
• ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY'S MANAGEMENT & EXECUTIVE STAFF
• ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY STAFF IN ALL DEPARTMENTS, INCLUDING ASSEMBLY OPERATORS & JANITORS. PERSONNEL WHO NEED HELP TO BE TRAINEED BY DEPARTMENT MANAGEMENT IN CONJUNCTION WITH QUALITY DEPARTMENT
• MEDICAL DEVICE COMPANY'S CONSULTANTS AND SUPPLY CHAIN PERSONNEL WITH ALL ABOVE DESCIPLINES
• MEDICAL DEVICE INDUSTRY VENTURE CAPITALISTS & INVESTORS WITH A NEED TO UNDERSTAND MEDICAL DEVICE DEVELOPMENT PROCESS OVERVIEW AND REQUIRED INFRASTRUCTURE
• ALSO, DESIGN, SUSTAINING, MANUFACTURING , QUALITY ENGINEERS AND OTHER DEPARTMENTAL STAFF FROM OTHER INDUSTRIES WHO HAVE DESIRE TO WORK IN MEDICAL DEVICE INDUTRY.

Target Audiences

• MEDICAL DEVICE INDUSTRY FORTUNE 500 AND STARTUP COMPANIES AND THEIR R & D ENGINEERING, MANUFACTURING ENGINEERING & OPERATIONS & QUALITY ENGINEERING AND DEPARTMENT EMPLOYEES, MEDICAL DEVICE DEVELOPMENT ENTREPRENUERS, MEDICAL UNIVERSITIES AND THEIR STAFF AND STUDENTS, ENGINEERING UNIVERSITIES – COLLEGES STAFF & BIOMEDICAL ENGINEERING STUDENTS & OTHER ENGINEERING DESCIPLINES
• DOCTORS, NURSES, HOSPITAL STAFF, HEALTHCARE INDUSTRY PERSONNEL WITH DESIRE TO UNDERSTAND HOW MEDICAL DEVICES ARE DEVELOPMED AND MANUFACTURED IN COMPLIANCE WITH THE FDA & INT'L REGULATIONS INCLUDING SAFETY & EFFICACY
• ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY'S MANAGEMENT & EXECUTIVE STAFF
• ESTABLISHED & STARTUP MEDICAL DEVICE COMPANY STAFF IN ALL DEPARTMENTS, INCLUDING ASSEMBLY OPERATORS & JANITORS. PERSONNEL WHO NEED HELP TO BE TRAINEED BY DEPARTMENT MANAGEMENT IN CONJUNCTION WITH QUALITY DEPARTMENT
• MEDICAL DEVICE COMPANY'S CONSULTANTS AND SUPPLY CHAIN PERSONNEL WITH ALL ABOVE DESCIPLINES
• MEDICAL DEVICE INDUSTRY VENTURE CAPITALISTS & INVESTORS WITH A NEED TO UNDERSTAND MEDICAL DEVICE DEVELOPMENT PROCESS OVERVIEW AND REQUIRED INFRASTRUCTURE
• ALSO, DESIGN, SUSTAINING, MANUFACTURING , QUALITY ENGINEERS AND OTHER DEPARTMENTAL STAFF FROM OTHER INDUSTRIES WHO HAVE DESIRE TO WORK IN MEDICAL DEVICE INDUTRY.