SeerPharma’s Post

Another wonderful year for the team here at SeerPharma. Our annual snapshot below offers a glimpse into the remarkable reach and impact we've achieved over the past 12 months. From solving complex, business-critical Quality and GMP challenges for our clients to strengthening our strategic partnership with MasterControl, it’s been a year of growth and innovation. This year, we celebrated some key milestones, including welcoming over 100 students into our Postgraduate GMP Program at the University of Technology Sydney— an achievement we are proud to support as we help cultivate the next generation of GMP professionals. On the commercial front, the growth of our network has been truly phenomenal. Back in April 2016, our database included just over 3,000 individuals. Today, we’re connected to more than 12,500 professionals from nearly 4,000 companies involved in the manufacturing of pharmaceuticals and medical devices. Looking ahead, we’re thrilled about the high-quality projects in our pipeline. We are humbled by the trust our clients place in us to address their most pressing Quality and GMP challenges. Each new project not only allows us to deliver impactful solutions but also deepens our expertise, fuelling our continuous improvement and enabling us to serve our clients even better. This cycle of learning, growing, and delivering value is our flywheel for ongoing success—and we’re excited to keep it turning in the years ahead. Our overall efforts and results demonstrate how we continue to "Advance Quality and GMP Best Practices in the APAC region" for the pharmaceutical and medical device industries. #gmp #pharmaceutical #medicaldevices #quality #qualitymanagement #qualityassurance

🔍 Ready for Your Next GMP Inspection? Here Are 10 Steps to Ensure Success! 🔍 GMP inspections are critical in upholding quality, safety, and regulatory compliance in the pharmaceutical world. Here’s a quick roadmap to keep your team ready and confident: 1️⃣ Conduct Internal Audits: Identify gaps early and proactively address non-conformities. 2️⃣ Document Everything: Keep SOPs, batch records, and logs current and accessible. 3️⃣ Ensure Cleanliness: Maintain clean, organized facilities to prevent contamination. 4️⃣ Form an Inspection Team: Designate roles for efficient interaction with inspectors. 5️⃣ Review Past Reports: Learn from previous inspections to continuously improve. 6️⃣ Train Staff: Equip employees with the skills to handle inspection protocols. 7️⃣ Set Up a Readiness Plan: Organize tasks, timelines, and responsibilities. 8️⃣ Practice with Mock Inspections: Prepare your team under real inspection scenarios. 9️⃣ Plan an Inspection Route: Map out an efficient path for inspectors. 🔟 Establish a War Room: Centralize coordination and quick responses on inspection day. Consistent preparation is key to seamless inspections. By embedding these practices, your company builds a culture of compliance and readiness every day. 💼✅ Read more in our latest article: https://lnkd.in/dZcR9PQ3 #GMPInspection #PharmaCompliance #QualityAssurance #InspectionReady #ContinuousImprovement #GMPInsiders

𝗛𝗼𝘄 𝘁𝗼 𝗶𝗺𝗽𝗹𝗲𝗺𝗲𝗻𝘁 𝗚𝗠𝗣 𝗦𝘁𝗮𝗻𝗱𝗮𝗿𝗱𝘀 𝗶𝗻 𝗟𝗮𝗯 𝗙𝗮𝗰𝗶𝗹𝗶𝘁𝗶𝗲𝘀? Good Manufacturing Practice (GMP) standards are essential for maintaining high-quality and compliant lab operations. By implementing GMP, labs can ensure the accuracy and reliability of their results, meet regulatory requirements, and enhance overall operational efficiency. Let’s learn more about the key steps👀 #gmp #compliance #pharma #HighQualityStandards

Get your doubts cleared withbthis interactive training.

Quality Control in GMP Environment #GMP #Pharma #Pharmuni #Pharmatalks Please write a comment on this post to share the link of GMP FREE COURSE WITH EU APPROVED CERTIFICATION with you

Yet another elaborate session by Dr. Binh Nguyen on day 2 guiding attendees at the 4th Annual Pharma GMP and Quality Management 2024 with Audit Readiness Strategies for proactive compliance. #eminencegroupventures #eminencebusinessmedia #ebmgmp4

For nearly a decade, SeerPharma has been a strategic partner of MasterControl. In that time we've deployed their advanced software solutions to automate Quality management and Manufacturing workflows for over 100 pharmaceutical and medical device companies across the APAC region. MasterControl has recently released electronic Logbooks, as part of their ongoing mission to solve business-critical problems in regulated manufacturing environments. Learn more about electronic Logbooks here: https://lnkd.in/gCQMMgBu In light of this launch, we are hosting a webinar on Wednesday the 30th of October from 2pm - 3pm AEDT. Fellow SeerPharma Director Andrew Giles will offer insights on the use of paper logbooks in our industry. Andrew will provide an overview of why regulatory bodies, including the US FDA, TGA, and other PIC/S authorities, mandate the use of logbooks. He will also discuss common challenges with paper logbooks and frequent GMP non-compliance issues. Director Rohan Bhatia and Business Development Manager Anil Pendurthi will then walk you through the latest advancements in electronic Logbooks from MasterControl. To register for this webinar, visit the page below, or click here: https://lnkd.in/gCiqmehG We look forward to seeing you there! Ciarán O'Keeffe Sara Bresee #quality #gmp #logbooks #elogbooks #saas #pharmaceuticalmanufacturing #pharmaceutical #medicaldevice #medicaldevicemanufacturing #medtech

Join us for a complimentary webinar looking at challenges with paper logbooks from a GMP compliance perspective and what can be done to address them. https://hubs.li/Q02TmhX10

Yet another elaborate session by Dr. Binh Nguyen on day 2 guiding attendees at the 4th Annual Pharma GMP and Quality Management 2024 with Audit Readiness Strategies for proactive compliance. #eminencegroupventures #eminencebusinessmedia #ebmgmp4

Find out why more and more users in Pharma and Logistics are switching over to digital management solutions to maintain GxP, GMP and 21CFR part 11 compliance.