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Results for tag: "Product Development"

Design Input: How to write requirements and modularize a product - Product Thumbnail Image

Design Input: How to write requirements and modularize a product

  • Training
  • 60 Minutes
  • Global
Change Control - Implementation and Management - Product Thumbnail Image

Change Control - Implementation and Management

  • Training
  • 60 Minutes
  • Global
10 Steps to Effective Risk Analysis for US FDA and ISO 14971 Compliance - Product Thumbnail Image

10 Steps to Effective Risk Analysis for US FDA and ISO 14971 Compliance

  • Training
  • 60 Minutes
  • United States
Cleaning Validation Regulations for Biopharmaceuticals: Strategies for Compliance - Product Thumbnail Image

Cleaning Validation Regulations for Biopharmaceuticals: Strategies for Compliance

  • Training
  • 60 Minutes
  • Global
The FDA Inspection: Best Practices for Preparation, Management, and Follow-Up - Product Thumbnail Image

The FDA Inspection: Best Practices for Preparation, Management, and Follow-Up

  • Training
  • 60 Minutes
  • Global
Pre-Market Submission Implications of FDA's Human Factors Guidance and Device Priority List - Product Thumbnail Image

Pre-Market Submission Implications of FDA's Human Factors Guidance and Device Priority List

  • Training
  • 90 Minutes
  • Global
Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance - Product Thumbnail Image

Writing Effective Clinical Evaluation Reports as Part of Post-Market Surveillance

  • Training
  • 60 Minutes
  • Global
Creating a Global Regulatory Plan - Product Thumbnail Image

Creating a Global Regulatory Plan

  • Training
  • 60 Minutes
  • Global
Documentation Requirements for Master and Working Cell Banks - Product Thumbnail Image

Documentation Requirements for Master and Working Cell Banks

  • Training
  • 60 Minutes
  • Global
Do you understand the FDA Guidance "Recognition and Use of Consensus Standards"? - Product Thumbnail Image

Do you understand the FDA Guidance "Recognition and Use of Consensus Standards"?

  • Training
  • 60 Minutes
  • Global
Updated EU filing and registration procedures (including the new variation rules coming in to force) - Product Thumbnail Image

Updated EU filing and registration procedures (including the new variation rules coming in to force)

  • Training
  • 60 Minutes
  • Europe
Selecting the Most Appropriate Predicate Device(S) for your 510(k) Application - Product Thumbnail Image

Selecting the Most Appropriate Predicate Device(S) for your 510(k) Application

  • Training
  • 60 Minutes
  • Global
How to Withstand an FDA Audit of your Facility - Product Thumbnail Image

How to Withstand an FDA Audit of your Facility

  • Training
  • 60 Minutes
  • Global
FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance - Product Thumbnail Image

FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance

  • Training
  • 70 Minutes
  • Global
The U.S. FDA's New Global Engagement Initiative - Product Thumbnail Image

The U.S. FDA's New Global Engagement Initiative

  • Training
  • 90 Minutes
  • United States, Global United States, Global
Best Practices for Maintaining an IND and IDE Application with FDA - Product Thumbnail Image

Best Practices for Maintaining an IND and IDE Application with FDA

  • Training
  • 60 Minutes
  • Global
Life Cycle Validation of GMP Potency Bioassays - Product Thumbnail Image

Life Cycle Validation of GMP Potency Bioassays

  • Training
  • 90 Minutes
  • Global
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Product Thumbnail Image

Analytical Test Methods Validation: FDA, ICH and USP Requirements

  • Training
  • 90 Minutes
  • Global
Risk Management Activities during Design Input - Product Thumbnail Image

Risk Management Activities during Design Input

  • Training
  • 60 Minutes
  • Global
How to Transfer Non-Compendial and Developed QC Procedures - ICH and USP Guidelines - Product Thumbnail Image

How to Transfer Non-Compendial and Developed QC Procedures - ICH and USP Guidelines

  • Training
  • 90 Minutes
  • Global
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Product Development is a key component of Production and Quality Management. It involves the design, testing, and implementation of new products and services. It is a process that requires collaboration between multiple stakeholders, including engineers, designers, marketers, and production personnel. The goal of product development is to create a product that meets customer needs and is cost-effective to produce. Product Development involves a number of activities, such as market research, concept development, prototyping, testing, and production. It is important to ensure that the product meets customer requirements and is of high quality. Quality assurance is an important part of the product development process, as it ensures that the product meets the desired standards. Companies in the Product Development market include Apple, Microsoft, Amazon, Samsung, and Google. These companies are leaders in the industry, offering innovative products and services to their customers. Show Less Read more