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Results for tag: "Product Development"

Major CGMP Issues - US FDA Concerns in 2022 - Product Thumbnail Image

Major CGMP Issues - US FDA Concerns in 2022

  • Training
  • 90 Minutes
  • United States
Understanding and Implementing a Technology Transfer Process - Product Thumbnail Image

Understanding and Implementing a Technology Transfer Process

  • Training
  • 60 Minutes
  • Global
Design History Files and Technical Files under US FDA and EU MDD - Product Thumbnail Image

Design History Files and Technical Files under US FDA and EU MDD

  • Training
  • 60 Minutes
  • United States, Europe United States, Europe
Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies - Product Thumbnail Image

Practical Process Validation Part 2 - Qualification Steps, Process Controls and Sustainability Strategies

  • Training
  • Global
Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices - Product Thumbnail Image

Practical Process Validation Part 1 - Validation Planning, Prerequisites and Best Practices

  • Training
  • 90 Minutes
  • Global
Does your QC lab do GMP and non-GMP activities? - Product Thumbnail Image

Does your QC lab do GMP and non-GMP activities?

  • Training
  • 60 Minutes
  • Global
Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3 - Product Thumbnail Image

Design Control / Ddesign and Development Requirements / Documents Under 21 CFR 820/ ISO 13485 7.3

  • Training
  • 90 Minutes
  • Global
The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs - Product Thumbnail Image

The New US FDA 21 CFR 820, Quality Management System Regulation (QMSR), Medical Device CGMPs

  • Training
  • 90 Minutes
  • United States
Drug Labeling and Packaging: Meeting Regulatory Requirements - Product Thumbnail Image

Drug Labeling and Packaging: Meeting Regulatory Requirements

  • Training
  • 60 Minutes
  • Global
US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes - Product Thumbnail Image

US FDA Medical Device QSR (21 CFR 820) / Quality Management System - current and proposed major changes

  • Training
  • 90 Minutes
  • United States
The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process - Product Thumbnail Image

The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process

  • Training
  • 90 Minutes
  • Global
European Filing and Registration Procedures - Product Thumbnail Image

European Filing and Registration Procedures

  • Training
  • 90 Minutes
  • Europe
Process Validation - Current Industry Practices and FDA Guidance Document Review - Product Thumbnail Image

Process Validation - Current Industry Practices and FDA Guidance Document Review

  • Training
  • 60 Minutes
  • Global
Russia: Compliance Processes and Regulations - Product Thumbnail Image

Russia: Compliance Processes and Regulations

  • Training
  • 90 Minutes
  • Russia
Preparing for a U.S. FDA Audit - Product Thumbnail Image

Preparing for a U.S. FDA Audit

  • Training
  • 60 Minutes
  • United States
Hazard Analysis & Risk Management - New 14971 - Product Thumbnail Image

Hazard Analysis & Risk Management - New 14971

  • Training
  • 90 Minutes
  • Global
Quality Planning Process and Procedure - Product Thumbnail Image

Quality Planning Process and Procedure

  • Training
  • 60 Minutes
  • Global
Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Risk Management - Product Thumbnail Image

Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Risk Management

  • Training
  • 60 Minutes
  • Global
Design Controls: What to know when it comes to FDA regulated industry? - Product Thumbnail Image

Design Controls: What to know when it comes to FDA regulated industry?

  • Training
  • 120 Minutes
  • Global
Design Controls Basics - From Design Inputs to Design Outputs and Effective Design Transfer - Product Thumbnail Image

Design Controls Basics - From Design Inputs to Design Outputs and Effective Design Transfer

  • Training
  • 60 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