PCI Pharma Services Premium sponsor
PCI Pharma Services is a leading global Contract Development and Manufacturing Organisation (CDMO), providing comprehensive pharmaceutical solutions from early-stage drug development through clinical trials, commercial manufacturing, packaging and distribution. With over 8,000 employees across 38 GMP facilities worldwide, PCI combines industry-leading expertise, innovative technologies and a commitment to quality to support pharmaceutical and biotechnology companies in bringing life-changing therapies to patients.
PCI offers an extensive range of services, including sterile and non-sterile drug development and manufacturing, clinical trial services, advanced drug delivery solutions, drug-device combination products and commercial packaging. Its integrated capabilities help clients navigate complex pharmaceutical supply chains while maintaining the highest standards of regulatory compliance, efficiency and product quality. Through strategic partnerships, continuous investment and innovation, PCI is committed to accelerating drug development, improving clinical trial operations and ensuring reliable global access to essential medicines.
“Inspired by Tomorrow. Let’s Talk Future.”
PCI continues to advance pharmaceutical innovation and support the delivery of life-changing therapies to patients worldwide.
Gold Sponsors
PRONAV Clinical
PRONAV Clinical, a specialist in clinical trial supply, helps emerging biotech and pharma innovators reach early-phase trials faster and at lower cost, by accelerating and de-risking the clinical supply chain. Our expertise combines specialist project management, rapid onboarding and precise operational execution, with PROMAP, our proprietary task and document management platform, at the core of our service. As a small, highly responsive, boutique team, our customers benefit from a scalable, long-term partnership with a solutions-driven vendor who is committed to making your program a priority.
With transatlantic depots in Ireland and the US, PRONAV Clinical is ideally positioned to support global needs, including secondary packaging & labelling, QP batch certification and worldwide cold-chain distribution, ensuring that new therapies arrive safely and quickly to clinical trial sites worldwide whilst allowing our customers to focus on the science
Endpoint Clinical
Endpoint Clinical is a trusted clinical trial technology and service partner that delivers reliable RTSM solutions. Endpoint is committed to blending seamlessly into clinical trial processes by providing anticipatory and adaptive solutions to proactively mitigate risks. Endpoint’s decades of experience guarantees a deep understanding of the problems sponsors and CROs often face in clinical trials.
Endpoint’s tech-forward dedication to innovation and investment enables the company to control the controllables and proactively generate speedy and strategic solutions, so sponsors and CROs can focus on a seamless clinical trial. Through its Bluefin data and analytics capabilities, Endpoint further empowers clinical teams with actionable insights that support informed decision-making throughout the trial lifecycle.
Smurfit Westrock
Smurfit Westrock is a global leader in sustainable paper and packaging solutions. Its dedicated Adherence & Clinicals business unit provides specialised support to the pharmaceutical, biotechnology and clinical trials sectors, developing patient-centric solutions that improve medication adherence, optimise packaging efficiencies and support complex clinical and commercial supply chains.
Combining technical expertise with innovative thinking, Smurfit Westrock delivers clinical trial and regulated secondary packaging solutions, including child-resistant, senior-friendly packaging, wallets, kit cartons and extended-content labels. Committed to advancing the pharmaceutical industry, Smurfit Westrock has collaborated with pharmaceutical partners on the development of Digital Display Labelling (DDL). Through its work with the International Society for Pharmaceutical Engineering (ISPE), the company continues to support the infrastructure required for DDL adoption.
Smurfit Westrock has also invested in a purpose-built white room supporting secondary packaging testing at temperatures ranging from 2°C to 8°C, -25°C and down to -86°C. Combined with accelerated ageing capabilities, this investment strengthens clinical trial packaging validation.
While packaging is its business, developing solutions is its strength.
NUVALEZ Consulting Limited
Nuvalez Consulting is an Irish boutique pharmaceutical consultancy providing hands-on support across the product lifecycle, from protocol conversion and clinical development through product launch, commercialisation and ongoing supply.
Working with pharmaceutical and life sciences organisations across Europe, the United States and international markets, Nuvalez combines personal service with global capability. Its consultants work as an extension of client teams, building close relationships, understanding operational challenges and remaining accountable for results. With more than 25 years of industry experience, Nuvalez offers expertise across clinical trial drug supply, clinical and commercial logistics, supply planning, material requirements planning, serialization, validation, project management, master data, analytics and supply chain technology. The company also supports EU product launches, 3PL selection, supply chain due diligence and specialist resourcing.
Nuvalez has developed CONNECT AI, an intelligent supply planning platform that brings fragmented data into one governed environment. By automating data collection, cleansing and consolidation, CONNECT AI improves visibility, reduces manual effort and enables faster decisions.
Combining strategic insight with operational execution, Nuvalez helps clients design and manage the processes, systems and partnerships required to build compliant, resilient and scalable pharmaceutical supply chains.