Workshop: Strengthening Quality System in Traditional and Health Supplements Manufacturer: From Product Review to Quality Control Testing

Introduction

This workshop provides an in-depth understanding of key quality system requirements for Traditional and Health Supplements (TMHS) manufacturers, focusing on product review, verification, and quality control testing in compliance with current regulatory expectations.

Date: 29 & 30 September 2026 (2 Full Days)

Venue: National Institutes of Health (NIH), Setia Alam
Closing Date: 21 September 2026 (11:59 PM)
Seat Limit: Capped at 200 participants (First-come, first-served)

🎟️ Ticket Categories & Fees

Government Agencies: RM 250
Normal Rate (Ends 21 Sept 2026): RM 500 (first come first served)

⚠️ IMPORTANT : Day 2 Breakout Sessions During registration, you MUST select whether you are from a TMHS Manufacturer OR a QC Panel / Private Laboratory. This ensures you are assigned to the correct case study group on Day 2.

📝 How to Register

Please read the FAQ before you register

PROGRAM AGENDA

Day 1

Day 1 focuses on the regulatory and quality requirements for TMHS manufacturers, with practical discussions on Product Quality Review (PQR), GMP inspection experiences, verification of equipment, utilities and processes, and QC testing methods. Participants will also gain an overview of the registration process for natural products and health supplements, supported by sharing sessions from manufacturers and QC professionals.

Day 2

Day 2 focuses on practical case studies and real-world applications related to TMHS quality and regulatory requirements. Participants will explore TMHS case studies, NPRA private laboratory applications, industry experiences, and common quality-related challenges, followed by interactive case presentations and Q&A sessions to enhance practical understanding and knowledge sharing.

🌿 What to Expect at the Workshop

Join us for two days of practical learning and meaningful discussions designed to strengthen quality systems in Traditional & Health Supplements (TMHS) manufacturing.

Participants can look forward to:
✨ Insights on Product Quality Review (PQR)
🔍 Practical approaches to equipment, utilities and process verification
🧪 Understanding QC methods and testing requirements
🏛️ Updates on registration processes for natural products & health supplements
💬 Sharing sessions with manufacturers and QC professionals
📚 Real-world case studies and practical examples
❓ Interactive Q&A sessions addressing common GMP and quality-related challenges

📅 29–30 September 2026
📍 National Institutes of Health (NIH), Setia Alam
⏰ 8:30 AM – 5:00 PM

Come prepared to learn, share experiences and strengthen your approach to quality assurance in TMHS manufacturing.

Elevating Quality. Ensuring Safety. Protecting Health.

Speakers

MS AIDA HARYATI BINTI ABDUL RAHIM

Head of Good Manufacturing Practice (GMP), National Pharmaceutical Regulatory Agency (NPRA)

MS IDA SYAZRINA BINTI IBRAHIM

Senior Principal Assistant Director, National Pharmaceutical Regulatory Agency (NPRA)

MR ABDUL HAKIM BIN MOHD ISA

Senior Principal Assistant Director, National Pharmaceutical Regulatory Agency (NPRA)

MS ALYAA BINTI ISMAIL

Senior Principal Assistant Director, National Pharmaceutical Regulatory Agency (NPRA)

MS TAN XIN CI

Principal Assistant Director, National Pharmaceutical Regulatory Agency (NPRA)

Venue

National Institutes of Health (NIH) Malaysia

Jalan Setia Murni U13/52, Seksyen U13, Bandar Setia Alam, 40170 Shah Alam, Selangor, Malaysia

Let us know if you'll be attending!

RSVP

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