Course Name
Control Plan
Course Overview
Welcome to the Control Plan Training by ARG Academy. This program provides a structured approach to understanding the purpose and scope of a Control Plan within the context of AIAG Core Tools. It guides participants through the systematic development and maintenance of Control Plans that align with Advanced Product Quality Planning (APQP) and support continuous improvement.
Course Objective
This course aims to provide delegates with the following knowledge:
● Understand the purpose and scope of a Control Plan in the context of AIAG Core Tools.
● Identify and define the key elements of an AIAG Control Plan.
● Differentiate between the types of Control Plans: Prototype, Pre-Launch, Safe Launch, and Production.
● Develop and maintain a Control Plan that aligns with APQP and supports continuous improvement.
● Integrate the Control Plan with other quality tools such as Process Flow Diagrams and FMEA (Failure Mode and Effects Analysis).
Course Benefits
By participating in this training, delegates will be able to:
● Effectively identify key elements of a methodology, including product/process characteristics, classification, control methods, and reaction plans.
● Understand the essential linkages between core tools, specifically how to bridge Process Flow Diagrams, FMEA, and Control Plans.
● Implement a step-by-step procedure for developing Control Plans involving cross-functional teams.
● Master the management of quality document, including when to perform updates and how to handle change control and document management.
Who Must Attend
This course is suitable for quality professionals, engineers, production supervisors, and any personnel involved in product development, quality management, or continuous improvement activities who need to understand or implement Control Plans within an manufacturing environment.
Methodology
The training is delivered as a 7-hour program featuring an interactive approach:
● Modules: The course is divided into five core modules covering the definition, key elements, linkages to core tools, development procedures, and management/updating of Control Plans.
● Practical Activities: Delegates will engage in hands-on activities, including:
– Developing a Process Flow for a sample product.
– Developing a quality document for a sample product.
– Auditing a core tools.
● Discussion: The session includes summary recaps and open Q&A sessions to ensure clarity on all key concepts.
Course Duration
● This is a 7-hour course run over one day.
● The training schedule is from 9:00 am to 5:00 pm.
Frequently Asked Questions (FAQ)
How does a Control Plan relate to APQP and FMEA?
It is a critical output of the Advanced Product Quality Planning (APQP) process. It directly links to the risks identified in your Process Failure Mode and Effects Analysis (PFMEA), providing a structured summary of the systems used to minimize process and product variation.
What are the three distinct phases covered in this document?
Automotive manufacturers must develop this documentation for three specific phases: Prototype, Pre-launch, and Production. Our training covers the strict requirements for transitioning through all three phases to ensure full IATF 16949 compliance.
HRD Corp Claimable Course
This is a 100% HRD Corp Claimable Training
Stop letting your monthly levy sit idle. Upgrade your workforce with our fully approved corporate training programs under the HRD Corp Claimable Course.
Why Choose ARG Academy?
● No Out-of-Pocket Cash: Fees are deducted directly from your e-TRiS account.
● Certified Trainers: All programs are led by HRD Corp TTT-approved experts.
● Zero Paperwork Hassle: We assist you with the entire grant application process.
● Flexible Programs: Tailored courses in Leadership, Digital Skills, Sales, and Soft Skills.
Secure Your Training Grant Today
Don’t let your training budget go to waste this year while regulatory requirements continue to tighten. Equip your team with the skills they need to ensure total medical device compliance. Book your corporate Control Plan training slot today and empower your QA team. Click the Enquiry button below to reserve your seats now.
