PharmEng Technology

🔍 Explainable AI (XAI): Shaping the Future of Pharmaceuticals with Transparency and Trust In the fast-evolving world of pharmaceuticals, AI is unlocking groundbreaking possibilities—from accelerating drug discovery to enhancing patient care. Yet, as these advanced models become more complex, they bring challenges around transparency and regulatory compliance. Enter Explainable AI (XAI)—the tool that brings clarity to AI’s decision-making, with techniques like SHAP and LIME transforming intricate algorithms into understandable insights that meet FDA and EMA standards. At PharmEng Technology, we’re committed to bridging the gap between powerful AI and the transparency needed to stay regulatory-ready. By adopting XAI, we help pharmaceutical and healthcare organizations leverage AI responsibly—fostering trust, advancing innovation, and ensuring compliance every step of the way. 🌐 𝐑𝐞𝐚𝐝𝐲 𝐭𝐨 𝐓𝐫𝐚𝐧𝐬𝐟𝐨𝐫𝐦 𝐀𝐈 𝐢𝐧 𝐏𝐡𝐚𝐫𝐦𝐚? 📩 𝐂𝐨𝐧𝐭𝐚𝐜𝐭 𝐮𝐬 𝐚𝐭 𝐢𝐧𝐟𝐨.𝐚𝐬𝐢𝐚@𝐩𝐡𝐚𝐫𝐦𝐞𝐧𝐠.𝐜𝐨𝐦 𝐨𝐫 𝐬𝐜𝐡𝐞𝐝𝐮𝐥𝐞 𝐚 𝐟𝐫𝐞𝐞 𝐚𝐬𝐬𝐞𝐬𝐬𝐦𝐞𝐧𝐭 𝐚𝐭 https://lnkd.in/gzCy4X95 𝐭𝐨 𝐞𝐱𝐩𝐥𝐨𝐫𝐞 𝐡𝐨𝐰 𝐗𝐀𝐈 𝐜𝐚𝐧 𝐞𝐦𝐩𝐨𝐰𝐞𝐫 𝐲𝐨𝐮𝐫 𝐨𝐫𝐠𝐚𝐧𝐢𝐳𝐚𝐭𝐢𝐨𝐧 𝐭𝐨 𝐢𝐧𝐧𝐨𝐯𝐚𝐭𝐞 𝐰𝐢𝐭𝐡 𝐜𝐨𝐧𝐟𝐢𝐝𝐞𝐧𝐜𝐞 𝐚𝐧𝐝 𝐜𝐥𝐚𝐫𝐢𝐭𝐲. 📖 Discover more about XAI’s role in regulatory compliance, patient safety, and the future of AI-driven medicine 👉 https://lnkd.in/g2MGyHHW #PharmEngTechnology #ExplainableAI #PharmaceuticalInnovation #AIinPharma #RegulatoryCompliance #TransparentAI #HealthcareTech #AICompliance #DrugDiscovery #TrustworthyAI

As we wrap up the final day of the VNPCA & ISPE Singapore Affiliate EU GMP Workshop 2024 here in Ho Chi Minh City, we want to extend a heartfelt thank you to all the participants whose enthusiasm and engagement have made this event unforgettable. Your passion for advancing excellence in GMP compliance and pharmaceutical innovation inspires us at PharmEng Technology! We’re especially grateful to VNPCA and ISPE Singapore for organizing this impactful workshop and providing a platform for meaningful connections and knowledge-sharing. We look forward to seeing how these new ideas and partnerships will shape the future of pharma. To stay connected or learn more about our services, reach out to us anytime at info.asia@pharmeng.com. Here’s to a bright future of innovation and collaboration! 🚀 #PharmEngTechnology #ISPESingapore #VNPCA #GMPCompliance #PharmaInnovation #ThankYou #Networking #PharmaceuticalExcellence #FutureOfPharma #TogetherWeAdvance

🌟 We are excited to be part of the VNPCA & ISPE Singapore Affiliate EU GMP Workshop 2024, taking place at the Mai House Hotel in Ho Chi Minh City, #Vietnam ! PharmEng Technology is stationed at table #4, and our expert team Ir. Dr. Nizamil Fairuz Yahya, Dody Tanusubandi, and Roseline Tio is eager to connect with industry leaders and professionals. This event is an excellent opportunity to explore the latest in EU GMP regulations, exchange ideas, and foster collaborations within the pharmaceutical industry. With tomorrow marking the final day of the workshop, we invite you to visit our table, engage in meaningful discussions, and discover how we can support your organization's growth and compliance needs. Are you ready to take your knowledge to the next level? Don’t hesitate to reach out to us at info.asia@pharmeng.com for more information. Looking forward to seeing you there! 🚀 #PharmEngTechnology #ISPESingapore #VNPCA #GMP #GMPCompliance #PharmaceuticalIndustry #RegulatoryExcellence #PharmaInnovation #Innovation #Collaboration #Networking #PharmaLeadership #FutureOfPharma #CSV #LifeSciences

위험 기반 CQV:효율성과 준수성 향상 – 1부🔍✨ 제약 및 바이오 기술 분야에서 리스크 기반 접근 방식을 채택하는 것은 성공의 열쇠입니다. 이 전략은 고위험 영역에 집중함으로써 효율성을 높이고, 엄격한 규정 준수를 보장하며, 제품 품질을 향상시킵니다. CQV 프로세스를 현대화하여 운영을 혁신하고 규제 기준에 더 잘 맞추는 방법을 알아보세요. 🔑 더 큰 효율성을 발휘하고 운영을 간소화하며, 규정 준수를 뛰어나게 달성하려면 진정으로 중요한 것에 집중하십시오. 최신 규제 표준에 맞춘 방법을 수용하고 제품 품질을 한 단계 끌어올리세요. 📈✅ 📖 위험 기반 CQV가 가져오는 혁신적 영향을 다룬 최신 기사를 확인하세요: https://lnkd.in/g4z7vaby 또한 맞춤형 인사이트를 위해 info.asia@pharmeng.com 으로 문의해 주세요. 📧🔗

23 Oct 2024, MITEC KL Exhibition Day 2 Summary: The key attractions at our booth during Day 2 was the AT-Log Sensing System design specifically for EMS which drew significant attention from visitors across multiple industries. This cloud-based wireless monitoring solution offers real-time data integrity and acquisition, powered by advanced LoRaWAN technology. Its low-cost and scalable architecture makes it an ideal solution for both continuous monitoring and project-based validation work. AT-Log Sensing System composed of sensors, gateways, cloud server, and web apps, offering a comprehensive Internet of Things (IoT) solution. Recommended for monitoring a controlled environments for warehouses, storage rooms, freezers, incubators, trucks, and vertical farms. The key system features include: #Real-time monitoring: Data is centrally collected and can be accessed in real-time through both desktop and mobile devices. #Alarm Systems: The system provides immediate alarm notifications when pre-set conditions deviate from norms, ensuring swift corrective action. #Scalability: The system supports an unlimited number of sensors, making it suitable for large-scale operations. #Accessability: Complete reporting and monitoring capabilities are available through a user-friendly web interface, facilitating easy data management. Throughout the day, we received inquiries from healthcare logistics companies particularly interested in the AT-Log System’s capabilities to support GMP & GDP compliance and validation processes, especially for temperature-sensitive shipments. Visitors appreciated the system’s flexibility for applications like temperature mapping, warehouse monitoring, and tracking environmental conditions in storage or transportation. Please come see us on the last day at booth #12 and meet our leads: Ts. Ahmad Safuan Dzakuan Hj. Mokhtar Qadly Ameen Pahlawi Syazirol Mazlan Looking forward for Day-3, the last day of the event. #pharmengtechnology #ems #mitec #exhibition #temperaturemapping #temperaturemonitoring #atlogsensors #dataloggers #cqv #csv #validation #compliance

🌟 Day 1 & 2 Highlights: PharmEng Technology at Malaysia Pharma & Healthcare Expo 2024! 🌟 From October 22nd to 24th, our expert team, Ts. Ahmad Safuan Dzakuan Hj. Mokhtar, Anieta Adnan, Qadly Ameen Pahlawi, and Syazirol Mazlan has been connecting with industry leaders, fostering meaningful conversations, and unlocking new collaboration opportunities. It’s been an exciting two days of sharing insights on how we elevate businesses through innovative compliance and quality assurance solutions. But it’s not over yet! 🔔 Tomorrow is the final day! Don’t miss your chance to visit us at Hall 5, #MITEC, Booth #F12 and discover how our expertise in Commissioning, Qualification, and Validation (CQV) is driving pharmaceutical innovation. Whether you’re looking to streamline operations, ensure regulatory compliance, or simply explore the future of the industry—we’ve got the answers! 💬 Have specific questions or need personalized advice? Reach out to us at the event by emailing info.asia@pharmeng.com for a free consultation. Let’s explore how PharmEng can partner with you on your journey to operational excellence. We can’t wait to connect with you on this final day! #PharmEngTechnology #PharmaExpo #PharmaceuticalExcellence #CQV #EngineeringCompliance #LifeSciences #HealthcareInnovation #MITEC2024 #MalaysiaExpo #TechTransfer #DataLogger #TemperatureMapping

🔑 Unlock the Secret to Pharma & Biotech Success: Early Regulatory Engagement! In today’s fast-paced pharmaceutical and biotech world, innovation is skyrocketing—AI is revolutionizing processes, and groundbreaking therapies are on the horizon. But there's one key element that can make or break your journey to market: navigating the regulatory maze! 🛣️ Early engagement with regulatory bodies isn’t just a smart move—it’s a game-changer. By getting ahead of compliance and validation early, you can fast-track approvals and ensure your products are market-ready in record time. ⏳ 💡 Curious how it works? Dive into our latest article to discover how proactive communication with regulators can set you on the fast track to success! 🔗 Read the Full Article: https://lnkd.in/gUs8K4_p ✉️ Got questions? Email us at info.asia@pharmeng.com 🌟 Why is Early Engagement a Game-Changer? 🌟 🔍 Early consultations with regulators align your plans with legal frameworks, ensuring smooth sailing from the start. 🔧 Tailored validation strategies eliminate compliance risks and sharpen your product quality. 📈 Continuous collaboration accelerates approvals, helping your innovations reach the market and patients faster! 💬 Now it’s your turn! How do you stay ahead of regulatory hurdles in your product development? We’d love to hear your insights—drop a comment below and join the conversation!👇 #PharmaEngTechnology #Pharmaceuticals #Biotechnology #RegulatoryCompliance #Innovation #AI #ProductDevelopment #FDA #EMA #Validation #Biotech

22 OCT 2024, Malaysia Pharma & Helathcare EXPO 2024, MITEC, KL, Malaysia Day-1 #MalaysiaPharmaHealthcareExpo PharmEng Technology at Malaysia Pharma & Healthcare Expo 2024! Our PharmEng booth located at the #MalaysiaPharmaHealthcareExpo at Hall 5, MITEC, Booth #F12. Please find our SME #SubjectMatterExperts, #CQV, #techtransfer, #datalogger, #temperaturemapping and other solutions and driving innovation across the #lifesciences industry. Ts. Ahmad Safuan Dzakuan Hj. Mokhtar Qadly Ameen Pahlawi Syazirol Mazlan Anieta Adnan Adnan 💡 Have specific questions or need advice? Contact us during the event at info.asia@pharmeng.com for free consultations and let's discuss how PharmEng can support your journey toward operational excellence. We look forward to seeing you there! #PharmEngTechnology #PharmaExpo #PharmaceuticalExcellence #ValidationEngineer #CQV #EngineeringCompliance #lifesciences #HealthcareInnovation #MITEC2024 #MalaysiaExpo

🔑 Unlock the Secret to Pharma & Biotech Success: Early Regulatory Engagement! In today’s fast-paced pharmaceutical and biotech world, innovation is skyrocketing—AI is revolutionizing processes, and groundbreaking therapies are on the horizon. But there's one key element that can make or break your journey to market: navigating the regulatory maze! 🛣️ Early engagement with regulatory bodies isn’t just a smart move—it’s a game-changer. By getting ahead of compliance and validation early, you can fast-track approvals and ensure your products are market-ready in record time. ⏳ 💡 Curious how it works? Dive into our latest article to discover how proactive communication with regulators can set you on the fast track to success! 🔗 Read the Full Article: https://lnkd.in/gUs8K4_p ✉️ Got questions? Email us at info.asia@pharmeng.com 🌟 Why is Early Engagement a Game-Changer? 🌟 🔍 Early consultations with regulators align your plans with legal frameworks, ensuring smooth sailing from the start. 🔧 Tailored validation strategies eliminate compliance risks and sharpen your product quality. 📈 Continuous collaboration accelerates approvals, helping your innovations reach the market and patients faster! 💬 Now it’s your turn! How do you stay ahead of regulatory hurdles in your product development? We’d love to hear your insights—drop a comment below and join the conversation!👇 #PharmaEngTechnology #Pharmaceuticals #Biotechnology #RegulatoryCompliance #Innovation #AI #ProductDevelopment #FDA #EMA #Validation #Biotech

CQV 디지털화: 제약 검증의 미래 수용하다 당신의 제약 검증 프로세스는 다음 시대를 준비하고 있습니까? PharmEng Technology는 운영을 간소화하고, 규정을 준수하며, 비할 데 없는 정밀도를 제공하는 첨단 디지털 도구를 통합하여 커미셔닝, 자격 부여 및 검증(CQV)을 혁신하고 있습니다. 디지털 CQV가 귀하의 프로세스를 어떻게 향상시킬 수 있는지 탐구해 보세요: ⏱ 검증 시간 단축 🔒 향상된 데이터 무결성 ✅ 규제 준수 향상 💰 비용 절감 📊 의사 결정 개선. 오늘 당신의 CQV를 변화시키세요! 📖 전체 기사를 보려면 https://lnkd.in/dRspVDvC를 방문하세요. 전문적인 조언이 필요하시면 info.asia@pharmeng.com으로 연락해 주세요.