Pharma IT

Making an Impact 🏅 Pharma IT is proud to announce that our company has earned a coveted Gold Medal from Sustainability Ratings provider, EcoVadis! In our latest rating, completed in October 2024, we scored in the 98th percentile — with advanced level scores across all four thematic areas. We believe we have a responsibility to do business in a way that is both beneficial to our stakeholders and limits any negative impact on the environment and broader society. This year, we've worked to reaffirm and expand our commitment to these efforts, and now we have the gold medal to show for it! If sustainable sourcing is part of your company's CSR strategy, we'd be happy to discuss how we are providing our customers with service they can be proud to include in their portfolios. You can check out our full announcement, here 🔗 https://lnkd.in/d4pdWGBJ If you'd like to know more about our CSR commitments & progress, feel free to reach out directly to Naomi Kellogg, who also leads the global CSR strategy implementation for the entirety of ProductLife Group.

🌱 Pharma IT is growing, and we’re on the lookout for IT Quality, Validation, and Compliance Consultants and IT Project Management Consultants! 🔍 We’re seeking several consultants to support our clients across the Nordics within the pharma, biotech, and medical device industries. 🔗 Check out the full job descriptions and apply today via Linkedin (links in the comments). 💡 Know someone ideal for these roles? Tag them in the comments below to help spread the word!

🚨 Early Bird Reminder: Save 15% Before the Year Ends! Time is running out to take advantage of our EARLYBIRD15 discount for 𝐄𝐔 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐀𝐟𝐟𝐚𝐢𝐫𝐬 – 𝐋𝐚𝐭𝐞𝐬𝐭 𝐔𝐩𝐝𝐚𝐭𝐞𝐬 𝐚𝐧𝐝 𝐄𝐱𝐩𝐞𝐫𝐭 𝐈𝐧𝐬𝐢𝐠𝐡𝐭𝐬, happening February 25, 2025, in Copenhagen. Join us for a full day of engaging sessions led by top regulatory experts including: • New EU Pharma Legislation • Orphan Medicines and the Impact of the New EU Pharma Legislation • Pediatric Development and Impact of the New EU Pharma Legislation • Clinical Trial Regulation • The EU PRIME Scheme • New EU Health Technology Assessment Regulation • Drug-Device Combinations in the EU ... and more! ✨ Use code EARLYBIRD15 for 15% OFF – valid only until the end of this year! Learn more and secure your seat here🔗 https://lnkd.in/eGBzzvgv We’d love to see you there 💙

We're #hiring a new IT Project Management Consultant in Copenhagen Municipality, Capital Region of Denmark. Apply today or share this post with your network.

👋 Meet Kirstine, Drug Safety & Pharmacovigilance Consultant at Pharma IT! With over 3 years of experience in pharmacovigilance, Kirstine specializes in drug safety operations across both clinical development and post-marketing phases. Her expertise spans EudraVigilance operations (including ICSR registration, uploading ICSRs, and ICSR and MLM downloads), aggregate reports, and scientific literature monitoring. 💼 Kirstine supports clients in their daily pharmacovigilance processes, including the processing and submission of ICSRs to ensure regulatory compliance. 🌟 What sets Kirstine apart is her strong attention to detail, commitment to high-quality work, and a thorough understanding of pharmacovigilance regulations. 💌 Looking for expert support in Drug Safety & Pharmacovigilance? Reach out to Sukhjit today to learn how Kirstine can assist with your compliance and safety needs! Read more about our Drug Safety & Pharmacovigilance Services here 🔗 https://lnkd.in/d8sCj5zQ

We're #hiring a new IT Quality, Validation, and Compliance Consultant in Copenhagen, Capital Region of Denmark. Apply today or share this post with your network.

💡#ICYMI: Our ProductLife Group sister company, Integrity is hosting a webinar on Computer Software Assurance (CSA). Join us tomorrow at 4PM CET! #CSV #CSA #GAMP5 #ITValidering

Navigating the complexities of Drug Safety & Pharmacovigilance can be challenging. That's why you need a partner you can trust 🤝 With over 55 years of combined experience, our team is committed to ensuring your drug development process is seamless, safe, and fully compliant. We can support you with ⤵️ ▪️ Expert guidance in Drug Safety Operations, including precise processing of Individual Case Safety Reports (ICSR) ▪️ EU QPPV and Deputy QPPV services ensuring compliance and expertise ▪️ Local QPPV/Safety Representative support for seamless regulatory compliance ▪️ Proactive PV Audits and Assistance with Inspections, guaranteeing readiness and excellence ▪️ Comprehensive Risk Management Plans (RMPs) and Aggregated Reports ▪️ Scientific Literature Monitoring ▪️ Pharmacovigilance System Master File (PSMF) documentation for regulatory compliance ▪️ Pharmacovigilance Training ▪️ and more..... With a deep understanding of your unique needs, we offer tailored solutions to ensure your drug safety efforts always meet regulatory standards. 💌 Looking for assistance with Drug Safety & Pharmacovigilance? Connect with Sukhjit Gill or reach out at sugi@pharmait.dk Learn more about the team and how we can support you here 🔗 https://lnkd.in/d8sCj5zQ

🎄✨ Highlights from our unforgettable Julefrokost at the Copenhagen Distillery! A night of sparkly Studio 54 outfits, Jeoparty, dancing, and festive cheers with our incredible team at Pharma IT. Here's to wrapping up a fantastic year, and looking forward to an even brighter 2025! 🌟🎁 #Julefrokost #PharmaIT

✨ At Pharma IT, we are proud to support the incredible work of EventyrJul, a Danish initiative that brings the magic of Christmas to children and families in need, 🎄 On Christmas Eve, EventyrJul creates a magical atmosphere by setting up a traditional Christmas dinner, decorating an impressive tree , and preparing personal Christmas gifts for the children. 🎅 This holiday season, we have made a donation to help fund their Christmas Eve event, spreading joy and festive cheer to those who could use it most. 🎁 To learn more about Eventyr Jul, and how you can support thier work, visit: https://lnkd.in/e9HxZZEM