PCI Pharma Services

You can still register for the free East Coast November ExpertXchange seminars! Join us at one of the co-hosted seminars with Avid Bioservices and Worldwide Clinical Trials, where we will explore strategies for drug development, manufacturing, and clinical trial excellence. Dates & Venues: - Raleigh, NC - November 12th | Embassy Suites by Hilton - Bridgewater, NJ - November 13th | The Bridgewater Marriott - Waltham, MA - November 14th | The Westin Waltham Boston Full seminar agenda, details & registration: https://lnkd.in/eVqp_xQS #ExpertExchange #DrugDevelopment #CDMO #LetsTalkFuture

News: PCI Pharma Services have been awarded a Gold rating in the Better Stands assessment by AbraxysGlobal Ltd for commitment to ESG at CPHI by applying sustainable principles to the design and afterlife of their stand. Our commitment to Environmental, Social, and Governance (ESG) principles goes beyond our facilities; we apply these values to all the events we participate in and host. At CPHI, our stand was designed and constructed using recyclable and reusable materials, including the framing and carpet. We also utilized energy-efficient LED lighting for all displays and fixtures. We know the impact we can make, locally and globally, and take great pride in demonstrating responsible and sustainable practices throughout our business. #ESG #Sustainability #LetsTalkFuture

In the latest PMPS supplement, PCI Pharma Services showcases comprehensive drug development, manufacturing, and packaging solutions. These solutions enhance product speed to market and create more significant opportunities for commercial success, emphasizing how advanced technology and ongoing investments meet global drug development needs throughout the product lifecycle - from manufacturing capabilities to clinical trial supply and commercialization. Click here to learn more: https://lnkd.in/dpfNWA9y   #CDMO #DrugDevelopment #PharmaManufacturing #LetsTalkFuture

Hear from Derek Truninger, General Manager at PCI Pharma Services, San Diego, as he shares valuable industry insights and how he sees data and data analytics playing a more significant role in the CTM space. With over 14 years of experience at PCI Pharma Services, I take pride in connecting with every department, team member, and client, offering direction, feedback, guidance, coaching, and mentorship whenever needed. PCI San Diego has experienced substantial growth in recent years, resulting in the site footprint doubling in size. This expansion has increased capacity and introduced new capabilities, including downstream sterile fill-finish processes. The facility now offers an integrated end-to-end solution for filling and packaging vials, syringes, and cartridges, with promising prospects for further expansion. Having played a vital role in the recent Sterile Fill/Finish expansion project, a solid organizational culture is essential for success. I work diligently to ensure that the San Diego facility is recognized as a preferred employer in the local community. My primary goal is to form a world-class organization built on solid quality principles, focusing on pristine customer service and driving a culture of collaboration, accountability, and ownership while taking pride in our role within the pharmaceutical industry. In the future, from a clinical supply perspective, I see the market growing into larger, rest-of-world studies, which requires not only a more extensive reach from a CDMO standpoint but also a deep understanding of the regulatory requirements across global jurisdictions to ensure compliance, for example, varying labeling needs and import/export permit requirements. Of course, data and data analytics are central to effectively and efficiently managing clinical trials. The scope and depth of data used in clinical trials are growing exponentially, and advanced analytics is turning this data into actionable insights that significantly impact trial outcomes. Data will continue to play a more prominent role in the CTM space. This may be full integration with IRT Systems, ERP Systems, or full-scale inventory management solutions that can better manage clinical supplies by supporting faster, more intelligent, and more efficient decision-making processes, from initial planning to regulatory submission. As trials become more complex, data-driven insights are beneficial and essential in navigating modern clinical research challenges. PCI Pharma Services is constantly evolving, creating capabilities and adding solutions for clients and potential clients, including deploying PCI | bridge™, our award-winning supply chain management platform, which helps clients instantly view their real-time global data for their clinical and commercial projects across our global sites. #CDMO #ExpertInsights #LetsTalkFuture

Press Release: We are delighted to announce that we won the prestigious 2024 Healthcare & Pharmaceutical Supply Chain Excellence Award for our digital supply chain management platform, pci | bridge™. The Supply Chain Excellence Awards set the standard for best practices in supply chain management around the globe. Renowned for their comprehensive judging process, the awards provide valuable insights to participants through feedback from a panel of esteemed judges, who together possess over 750 years of experience in the field. PCI Pharma Services has taken an assertive approach to digitization with pci | bridge™ as evidence of our commitment. With over four years of dedicated platform refinement, we are committed to further advancing our capabilities by introducing new features and enhancements driven by user feedback and emerging technologies. We are honored to be recognized for our digital supply chain management innovation. The power of experience. Let's talk future. More information: https://lnkd.in/epJiyq6s #SCEAUSA24 #ExperienceThePower #LetsTalkFuture

With more than 60% of the early-development pipeline coming from small, emerging, and virtual biotech companies, there is a great need to accelerate programs into clinical trials and secure additional funding. In addition, there are emerging classes of biomolecules that have huge potential to change disease treatment and companies are seeking to de-risk manufacturing operations. Robotic gloveless isolator sterile fill-finish systems address these needs. Jerome Detreille, Derek Truninger, and Peter Kim from PCI Pharma Services met with Pharma's Almanac Editor-in-Chief, David Alvaro, to discuss how PCI Pharma supports the accelerated timelines of client partners as they commence early-phase clinical trials with immediately available robotic SFF capacity at their clinical manufacturing and packaging facilities. #AsepticFillFinish  #Robotics  #CDMO  #LetsTalkFuture

We are delighted to announce that Tom McGrath, VP, Global Quality, Manufacturing and Development has been invited to speak at the upcoming PDA - Parenteral Drug Association New England Chapter FDA dinner meeting. With exceptional quality standards and regulatory compliance, and having recently successfully completed the International Coalition of Medicines Regulatory Authorities (ICMRA) multi-agency inspection at our Sterile Development and Manufacturing campus of excellence in Bedford, NH. Tom will share insights into how to successfully prepare and host an FDA inspection. For more information and how to join Tom and fellow guest speakers on 30 Oct, 5:30pm (UTC -4:00) Marlborough, MA: https://lnkd.in/gY6S5aF5 #CDMO #FDAInspection #SterileMAnufacturing #LetsTalkFuture

In today’s fast-paced industry, successful clinical trials require careful planning and execution. Precise forecasting and innovative kit design are essential for streamlining operations and expediting the release of new therapies. With the complexity of trials increasing, mastering these strategies means fewer disruptions, faster patient recruitment, and smoother trial execution. In this article published in the Journal of Clinical Studies, Slava Shulov, Senior Clinical Supply Manager at PCI Pharma Services, examines how advanced forecasting tools and flexible kit designs can positively impact clinical trial success. Learn more: https://lnkd.in/easnQ7-N #CDMO #ClinicalTrials  #DrugDevelopment  #LetsTalkFuture

Time is running out to book one of our November ExpertXchange series of free seminars! Accelerating Efficiency in Drug Development & Delivery: A Phase-Appropriate Approach. Join us at one of the co-hosted seminars with Avid Bioservices and Worldwide Clinical Trials, where we will explore strategies for drug development, manufacturing, and clinical trial excellence. This roadmap will emphasize phase-appropriate development to enhance efficiencies throughout the clinical trial journey towards the commercialization of biologic drug products. Dates & Venues: - San Francisco, CA - November 6th | Embassy Suites San Francisco Airport - San Diego, CA - November 7th | Marriot Del Mar - Raleigh, NC - November 12th | Embassy Suites by Hilton - Bridgewater, NJ - November 13th | The Bridgewater Marriott - Waltham, MA - November 14th | The Westin Waltham Boston Full seminar agenda, details & registration: https://lnkd.in/eVqp_xQS #ExpertExchange #DrugDevelopment #CDMO #LetsTalkFuture

We are proud to have been awarded a bronze medal by EcoVadis for our Sustainability Performance for the third consecutive year. For 2024, we improved our score from 54 to 58, putting us in the 66th percentile of more than 130,000 companies assessed by EcoVadis.  As we continue to grow, we are committed to reducing our environmental footprint, investing in greener technologies, and maintaining transparency in our sustainability efforts. By aligning with the highest ESG standards, we aim to positively impact both the communities we operate in and the environment at large. https://lnkd.in/eGiQKTdk #EcoVadis #ESG #Sustainability #LetsTalkFuture