PharmEng Technology

𝗗𝗮𝘆 𝟭 | ISPE Singapore Affiliate – 𝗩𝗡𝗣𝗖𝗔 𝗚𝗠𝗣 𝗪𝗼𝗿𝗸𝘀𝗵𝗼𝗽 𝟮𝟬𝟮𝟱 📍 Le Meridien Saigon Hotel, Ho Chi Minh City | November 6, 2025 PharmEng Technology was honored to participate in Day 1 of the ISPE Singapore – VNPCA GMP Workshop 2025, where industry leaders convened to advance excellence in pharmaceutical manufacturing and compliance. Our featured session, “Audit and Compliance: Cruciality in Implementing GMP Audits,” was presented by Ir. Dr. Nizamil Fairuz Yahya, highlighted the strategic importance of structured auditing as a cornerstone for enhancing operational performance, strengthening compliance frameworks, and driving continuous improvement within GMP-regulated environments. The presentation also provided valuable insights into the differences among EU, PIC/S, US FDA, and WHO GMP requirements, emphasizing the importance of a global regulatory perspective in navigating evolving compliance expectations and maintaining alignment with international quality standards. Visit PharmEng Technology at Tabletop #1 to connect with our experts Ir. Dr. Nizamil Fairuz Yahya, Dody Tanusubandi, and Roseline Tio., and explore how our integrated solutions in Pharma 4.0, CQV, and Engineering Design Services can help drive your organization’s journey toward operational excellence. #PharmEngTechnology #PharmEngTechnologyEFOR #ISPE #VNPCA #GMPWorkshop #PharmaCompliance #QualityAssurance #AuditExcellence #OperationalExcellence #PharmaInnovation #PharmaceuticalEngineering #LifeSciences #Vietnam #CQV #EngineeringDesign

🌏 VNPCA GMP/GMP-EU Workshop 2025 | Le Méridien Saigon, Vietnam 📅 Date 6 November 2025, 1st Day 📍 Organized by ISPE Singapore Affiliate It was overwhelming participation in the VNPCA GMP/GMP-EU Workshop held in Ho Chi Minh City, where regulators, industry experts, and professionals gathered to exchange insights on advancing Good Manufacturing Practice (GMP) implementation and regulatory harmonization across global standards. 11.50am, deliver a presentation on 🎤 “Cruciality in Implementing GMP Audits”, sharing perspectives on the importance of audit strategy, compliance culture, and continuous improvement as key enablers of sustainable GMP performance. The session also featured valuable insights into 🔍 “Differences Between EU, PIC/S, US FDA, and WHO GMP Requirements”, highlighting the nuances and expectations that drive global pharmaceutical compliance. Grateful to the ISPE Singapore Affiliate and VNPCA for this well-organized and impactful event — and to all participants for the engaging discussions and shared commitment toward elevating quality and compliance standards in the region. #GMP #ISPE #PharmaCompliance #Pharmaceutical #Industry #QualityCulture #RegulatoryAffairs #AuditExcellence #PharmEngTechnology #Vietnam

2nd Day Summary: 8 Oct 2025, PharmEng Technology at Malaysia Pharma & Healthcare Expo 2025 Venue: World Trade Centre Kuala Lumpur Booth: C1 – PharmEng Technology Representatives: Ir. Dr. Nizamil Fairuz Yahya. Ts. Ahmad Safuan Dzakuan bin Hj Mokhtar Muhammad Na’im S. HAMDAN MOHD ISA On the second day of the 2nd Malaysia Pharma & Healthcare Expo, PharmEng Technology continued to attract steady visitor engagement at Booth C1. Interest remained strong in the areas of Good Distribution Practices (GDP), environmental monitoring, and temperature/RH control systems within pharmaceutical facilities. 📍 Discussions with industry professionals and potential clients focused on: -         Implementation of GDP-compliant warehouse and cold chain systems -         Data-driven solutions for temperature and humidity mapping -         Validation and qualification services for GMP environments 💡 Many WHY questions being throw-up during this event: -         WHY is GDP compliance important for the supply chain? -         WHY do we need to perform Temp & RH mapping? -         WHY do we need to comply with such strict & stringent requirements? -         WHY should regulated industries e.g. Pharma, Medical Devices investing in data-driven, real-time monitoring solutions? -         WHY validation & qualification essential for GMP & GDP compliance? The second day also provided opportunities to connect with regulatory officers, pharmaceutical manufacturers, cosmetic and solution providers, enhancing visibility and collaboration potential. PharmEng Technology’s presence reinforced its role as a trusted partner in GMP and GDP compliance, with visitors recognizing the company’s expertise and practical solutions for maintaining quality and product integrity across the pharmaceutical supply chain. #PharmEngTechnology #PharmaExpo #PharmaceuticalExcellence #CQV #GMP #GDP #Compliance #Validation #HealthcareInnovation #MalaysiaPharmaHealthcareExpo #ATloge #Datalogger #TemperatureMapping #TemperatureMonitoring #EVMS

1st Day: 2nd Malaysia Pharma & Healthcare Expo – 7 October 2025 Venue: World Trade Centre Kuala Lumpur Booth: C1 – PharmEng Technology PharmEng Representatives: Ts. Ahmad Safuan Dzakuan bin Hj Mokhtar & @Muhamad Na’im Samsudin PharmEng Technology participated in the 2nd Malaysia Pharma & Healthcare Expo held on 7-9 October 2025 at the World Trade Centre Kuala Lumpur, showcasing at Booth C1. Represented by Ahmad and Naim, the team engaged with a high volume of visitors, reflecting strong industry interest in regulatory compliance and operational excellence. Key areas of inquiry centered around: - Good Distribution Practices (GDP) - Warehouse and storage temperature control - Relative humidity (RH) mapping and monitoring The booth saw active discussions on best practices, compliance standards, and technical solutions to ensure product integrity throughout the pharmaceutical supply chain. The event itselves served as a valuable platform for networking, knowledge exchange, and reinforcing PharmEng Technology's commitment to supporting the healthcare and pharmaceutical industries in Malaysia and the region. #pharmeng #technology #pharma #healthcare #exhibition #temperature-mapping #relativehumidity-mapping #data-logger #gdp-compliance #warehouse-storage—coldstorage

01 Oct 2025, AT Log Data Logger Deployment Activities A TIMELINE OF MODERN TECHNOLOGY Over the weekend, our team successfully executed key activities to support the deployment of AT Log Data Loggers and the accurate mapping of temperature and relative humidity (RH) within our client’s warehouse facilities. Recognizing the importance of maintaining the integrity of temperature and RH data—both for compliance and product safety—our team demonstrated exceptional commitment by ensuring all tasks were completed efficiently and to a high standard. Key Activities Completed: - Precise placement and calibration of data loggers across designated warehouse zones. - Real-time monitoring conducted to validate environmental consistency throughout the facility. - Data verification and review performed to ensure mapping accuracy, supporting future analysis and optimization. This effort underscores our commitment to operational excellence, proactive service delivery, and timely project execution. This integrated At-Log with EVMS (Environmental, Validation & Monitoring Systems) Platform Utilizing Internet of Things (IoT) technology for low-cost, highly-scalable system that combines both monitoring and logging capabilities, and cloudified for modern industries. Key Success Results: ✅ Compliance Confidence: Built for high-stakes environmental results where regulatory precision is non-negotiable. 📈 Operational Efficiency: Reduces manual validation efforts, accelerates release timelines and real-time monitoring. 🔍 Traceability & Transparency: Every data point is tracked, validated, and ready for inspection. 🧠 Smart Insights: Leverages analytics to predict risks and optimize environmental control strategies. Thanks & credit to the team: Muhammad Na'im S. HAMDAN MOHD ISA Rida Hadirah Ts. Ahmad Safuan Dzakuan bin Hj Mokhtar #pharmeng #technology #Temperature #RelativeHumidity #datalogging #mapping #FacilitiesManagement #Engineering #ProjectExecution #Professionalism #Compliance #OperationalEfficiency #Traceability #Transparncy #DataIntegrity #SmartInsights