DPR Construction’s Post

How are pharmaceutical companies overcoming critical piping challenges in an increasingly complex industry? The pharmaceutical industry is constantly evolving, and with it comes the need for advanced solutions to tackle intricate piping systems. Safety, efficiency and regulatory compliance are more important than ever. But how are leading companies navigating these challenges? Learn how engineering company TUREFEN leveraged Hexagon's CAESAR II® to overcome these challenges, driving significant improvements in project outcomes for one of its pharmaceutical clients. Discover how Hexagon is helping shape the future of pharmaceutical engineering. Read the full case study: https://hxgn.biz/4dzlTjv #PharmaceuticalEngineering #IndustryChallenges #Innovation

How are pharmaceutical companies overcoming critical piping challenges in an increasingly complex industry? The pharmaceutical industry is constantly evolving, and with it comes the need for advanced solutions to tackle intricate piping systems. Safety, efficiency and regulatory compliance are more important than ever. But how are leading companies navigating these challenges? Learn how engineering company TUREFEN leveraged Hexagon's CAESAR II® to overcome these challenges, driving significant improvements in project outcomes for one of its pharmaceutical clients. Discover how Hexagon is helping shape the future of pharmaceutical engineering. Read the full case study: https://hxgn.biz/4dzlTjv #PharmaceuticalEngineering #IndustryChallenges #Innovation

Blue Mountain and Catalent are excited to announce we are hosting a free webinar on "Equipment Criticality Assessment: The Consequence of the Failure Determines the Maintenance Effort". Register here to attend: https://lnkd.in/eUWBquCx . Attendees will learn about a best practice approach to understanding the relative importance of equipment assets to ensure you have appropriate strategies in place to care for your assets and minimize the risk of failures. This is especially relevant in the highly regulated pharmaceutical industry. Register here: https://lnkd.in/eUWBquCx #BlueMountainRAM #GMPDigitalMaturtityModel #RegulatoryAssetManager #AdvanceGMPcompliance

Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02lDlD90 #ISPE #gamp #ispetraining

Secure your spot now before time runs out. Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02q1r-j0 #ISPE #gamp #ispetraining

ECOVIDA hosted a theoretical and practical training in Pharmaceutical Technology, focused on Development, Technology Transfer, Productivity and Regulation. Our representatives had the opportunity to directly apply the acquired knowledge in real-world scenarios to face challenges and opportunities with confidence. It was more than a training, it was a step forward in building our future. #Partnersofthefutureinprogress #PharmaceuticalTechnology #PharmaceuticalDevelopment #ProfessionalTraining

📣 Exciting Webinar Announcement! Join us for an insightful session on the basics of "FDA Regulation" with Lee Leichter. 📅 Date: 25. September 2023 ⏰ Time: 16.00-17.00 CET 🧑⚕️ With nearly 50 years in the healthcare sector, Lee Leichter offers hands-on expertise to global Pharmaceutical, Biotechnology, and Medical Device firms, focusing on diverse business, technical, regulatory, and quality aspects, particularly within drug delivery and combination products across the USA, Europe, and Canada. If you’re interested in joining, email siro@peakspirit.ch with your name, company, and contact details. Looking forward to seeing you there! #HealthTech #Webinar #FDA #Regulations #MedTech #DigitalHealth

Many challenges in the pharmaceutical manufacturing space arise when important activity, including risk, is outsourced. A 2022 article in Outsourced Pharma shows that outsourcing is a common and essential activity in biopharmaceutical operations. (Credit: @Smita Khanna. BioPlan Associates, Inc.) https://lnkd.in/eRbN-K3Q The image below, from the article, shows the range of activities commonly outsourced. 💡 Ensuring that effective management strategies are in place is critical. This includes processes to manage knowledge about risk. 💡 Why not join PDA Ireland in Cork on the 29th Feb 2024 to discuss these challenges, and more, through the lens of both contract giver & receiver. As it is LEAP DAY - this is a great proposal! https://lnkd.in/eBvghwkf

Learn about regulatory requirements for computerized systems in the pharmaceutical, biotech, or medical device industry and explore tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements, by building upon existing industry good practice in an efficient and effective manner. Learn More: https://hubs.la/Q02mLyGF0 #ISPE #gamp #ispetraining

The pharmaceutical manufacturing industry is brimming with opportunities, with a forecast of $140 billion in capital projects for 2024. If your company has experience in other sectors and wants to tap into this lucrative market, our latest blog post is a must-read!  Learn how to:  - Align with cGMP standards  - Implement robust documentation practices  - Strategically enter the market  Read the complete guide to discover how your business can successfully transition and thrive in this growing industry.  https://lnkd.in/ee5WGeyz  #PharmaceuticalManufacturing #BusinessGrowth #cGMP #IndustryTransition