

LEARN MORE
with the knowledge and practical skills required to conduct highly effective
internal audits of Medical Device Quality Management Systems (QMS).
& Internal Audit Training
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professionals with the knowledge and practical skills required to conduct highly
effective internal audits of Medical Device Quality Management Systems (QMS).
& Internal Audit Training


LEARN MORE
and skills to plan, validate, review, and maintain radiation sterilization
processes (Gamma, Electron Beam, and X-ray) and to implement a
structured transition to ISO 11137-1:2025.
& Radiation Sterilization Practical Training
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and skills to plan, validate, review, and maintain radiation sterilization
processes (Gamma, Electron Beam, and X-ray) and to implement a
structured transition to ISO 11137-1:2025.
& Radiation Sterilization Practical Training


LEARN MORE
understanding of sterile barrier system requirements and packaging
process validation for sterile medical devices.
Training in ISO 11607-1 and ISO 11607-2
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understanding of sterile barrier system requirements and packaging
process validation for sterile medical devices.
Training in ISO 11607-1 and ISO 11607-2
HRDF Claimable Training
Join HRDF claimable training program by ARG Academy PLT.
Experienced Trainer
ARG Academy dedicated to enhance your QMS, and technical competencies.
Technical Training Solution
Compliance training for ISO 9001, ISO 13485, and medical device sterilization.
About Us
ARG Academy PLT (LLP0042529-LGN) is a professional training and development organization.
ARG Academy is dedicated to enhancing business, management, and technical competencies. At ARG Academy, we focuses on delivering structured training programs, professional development initiatives, and technical learning solutions designed to improve organizational capability, workforce performance, and operational effectiveness across various industries.
Through practical learning methodologies and industry relevant content, ARG Academy supports organizations and individuals in developing the skills, knowledge, and technical proficiency required to meet evolving business and operational demands.
Featured Courses
Integrated Training for Medical Device Auditors – Sterilization Technology Auditor (STA)
Course Name Integrated Training for Medical Device Auditors – Sterilization Technology Auditor (STA) Course...
Manufacturing Process Validation for Medical Devices
Course Name Manufacturing Process Validation for Medical Devices Course Overview Welcome to the Manufacturing...
IATF 16949:2016 Interpretation and Implementation
Course Name IATF 16949:2016 Training : Interpretation and Implementation Course Overview Welcome to the...
IATF 16949:2016 Internal Quality Audit
Course Name IATF 16949:2016 Internal Quality Audit Course Overview Welcome to the Training Outline...
Statistical Process Control
Course Name Statistical Process Control Course Overview Welcome to the Statistical Process Control (SPC)...
Measurement System Analysis
Course Name Measurement System Analysis Course Overview Welcome to the Measurement System Analysis (MSA)...
Control Plan
Course Name Control Plan Course Overview Welcome to the Control Plan Training by ARG...
Advance Product Quality Planning and Production Part Approval Process
Course Name Advance Product Quality Planning and Production Part Approval Process Course Overview Advanced...
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Latest Posts
ISO 13485:2016 Understanding and Internal Audit Training
Most medical device companies struggle with one critical question during an audit: When…
ISO 11137-1:2025 Sterilization for Healthcare Products Training
Compliance shouldn’t be a reactive scramble. It should be a proactive strategy. 🛡️…
Comprehensive Training on ETO Sterilization & Compliance for Sterile Medical Device Manufacturing
We are pleased to share that ARG Academy successfully conducted a 𝟱-𝗱𝗮𝘆 𝗶𝗻-𝗵𝗼𝘂𝘀𝗲…
Upcoming Public Training
29
Sep
2026ISO 13485 internal auditing training
ISO 13485 Internal Auditing Training: Bridging Theory to Practice for Medical Device Compliance Most medical device compliance failures don’t start on the manufacturing floor. They happen because of critical gaps missed during internal audits. Understanding ISO 13485:2016 isn’t just about satisfying regulators—it is the absolute…
- (September 30, 2026)
22
Jul
2026Application of Risk Management to Medical Devices
Most medical device compliance failures aren’t due to poor engineering. They happen because risk management wasn’t effectively applied throughout the product lifecycle. ISO 14971:2019 isn’t just a regulatory checkbox. It is the absolute backbone of patient safety and market success. To ensure your team is…
- 09:0017:30(July 23, 2026)
Testimonials


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