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Accenture’s Life Sciences group is committed to helping our clients better serve patients while achieving their business objectives and revolutionising how medical treatments are discovered, developed and delivered. We provide end-to-end Veeva Vault business services including solution planning, implementation, operational support, centre of excellences, as well as insight-driven services. We continue to be a Premiere Services Partner for both Development and Commercial Cloud in 2025.

BASE life science is a leading consultancy operating between business and technology, delivering data-driven solutions and expert consulting services to the life sciences industry. We help clients navigate complexity and make smarter decisions, providing end-to-end support on a global scale. We tailor our services to drive innovation, efficiency, and lasting impact. As a Veeva premier service partner, we leverage next-generation digital capabilities to accelerate our clients’ success. Learn more at www.baselifescience.com.

Cognizant helps our clients modernize technology, reimagine processes and transform experiences so they can stay ahead in our fast-changing world.

Our solutions for Life Sciences companies are driven by our vision to improve patient outcomes. By integrating digital transformation into your business strategy, we help you create a more intelligent, agile and high-performing enterprise – to accelerate research & development, enhance compliance processes and deliver innovative therapies to patients faster.

Let us help you discover new ways of operating so you can anticipate and act, as if on intuition. See how at www.cognizant.com.

TransPerfect is the world’s largest provider of language services and AI solutions for global business. From offices in over 140 cities on six continents, TransPerfect offers a full range of services in 200+ languages to clients worldwide. More than 6,000 global organizations employ TransPerfect’s GlobalLink® technology to simplify the management of multilingual content. With an unparalleled commitment to quality and client service, TransPerfect is fully ISO 9001 and ISO 17100 certified. TransPerfect has global headquarters in New York, with regional headquarters in London and Hong Kong. For more information, please visit our website at www.transperfect.com.

As a trusted Veeva partner, Aqurance maximizes the value of Veeva Development Cloud through seamless system integration, data migration, and workflow optimization. We combine our technical expertise with strategic organizational change management, advisory and managed services, clinical and quality systems support, and regulatory compliance to empower R&D teams. By accelerating digital adoption with confidence, ensuring business continuity, managing risk, and optimizing release processes, we build scalable, future-ready ecosystems that seamlessly connect people, processes, and technology across global R&D functions, driving sustainable innovation and operational excellence.

Arithmos is a consulting, technology, and services company dedicated to the Pharmaceutical, Biotech, and Medical Device companies. We specialize in guiding organizations through their digital transformation journey, helping them harness the power of technology-enabled solutions to drive efficiency, compliance, and innovation.

With a global team of industry experts, we bring deep expertise across the GxP-regulated landscape, delivering cutting-edge technologies and services in Drug Safety Pharmacovigilance, Regulatory Affairs, Clinical Development, Quality Assurance.

At Arithmos, we bridge the gap between technology and business in the Life Sciences industry. With deep expertise in Consulting, Technology, and Managed Services, we deliver end-to-end support tailored to the unique needs of Pharmaceutical, Biotech, and Medical Device companies.

We help our clients break down operational and technological silos by:

– Efficient Communication – fostering cross-functional collaboration that accelerates decision-making and drives innovation.
– Standardized Processes – implementing harmonized, regulatory-compliant workflows that boost operational consistency and quality.
– Optimized Costs – leveraging automation, data-driven insights, and flexible service models to reduce overhead and maximize return on investment.

Arithmos acts as a strategic partner, enabling our clients to accelerate product development, ensure compliance, and improve patient outcomes.

CluePoints is the premier Risk-Based Quality Management (RBQM) and Data Quality Oversight Software provider. We are leveraging the potential of artificial intelligence using advanced statistics and machine learning to determine the quality, accuracy, and integrity of clinical trial data both during and after study conduct. Aligned with guidance from the FDA, EMA, and ICH E6 (R3), CluePoints is deployed to support central and on-site monitoring, medical review, quality risk management and to drive a holistic Risk-Based strategy in all trials. Coupled with thought leadership and consulting expertise to aid pre-study risk assessment, identification of risk controls and solution implementation, you now have everything you need to adhere with global regulatory guidance. The result is positive clinical development outcomes, increased operational efficiency, lower costs and reduced regulatory submission risk as part of the industry paradigm shift to RBQM.

Epista Life Science is a team of experts working at the intersection of business priorities, technology advancements and compliance requirements. We are a trusted advisor to Life Science companies, with proven methodologies that enable them to perform at their best – and keep them there.

We are dedicated to defining and delivering process, technology, and compliance excellence, thereby enabling Life Science companies to operate better, safer, and faster in their ongoing efforts to improve health and well-being around the world.

fme Life Sciences is a proven provider of business and technology services supporting the migration and deployment of Content Services and ECM solutions in the Life Sciences Industry. We work with the Top 30 global pharmaceutical and medical firms, serving as trusted advisors and systems integration specialists across the Clinical, Regulatory, Quality, Safety, Medical and Manufacturing domains in Europe and North America. We provide our clients with an independent perspective of the solutions available and help them achieve the highest ROI and lowest TCO for their technology choices.

INCONSULT GmbH, established in 2002 and based in Duisburg, Germany, specializes in consulting services for the Life Sciences, Biotech, and Medical Device industries. We provide comprehensive support across Clinical Operations, Regulatory Affairs, Quality Management, and Medical Safety. As experts in industries with high compliance and quality requirements, we combine deep business process knowledge with technological expertise to deliver tailored solutions. Our approach considers the broader customer context rather than isolated projects, ensuring sustainable value. With a focus on digital transformation, our consultants and technical experts work to maximize the benefits of our clients’ investments, with the ultimate goal of achieving absolute customer satisfaction.

Jeev is a Sanskrit word that essentially means “the vital energy of life” or “Life” itself.

Jeev Lifeworks is a team of experts with extensive experience in implementation, integration and maintenance of Safety, Clinical and Regulatory applications for large/medium/small Pharma, Biotech companies and CROs. We offer high quality, cost-effective and innovative services. Being an ISO 9001:2015 and ISO 27001:2013 certified company we employ a robust/advanced quality and information security management systems.

Our Core Competencies include Data Migration, Cloud Migration, Validation, Safety Database implementation, Reporting & Analytics, Enterprise Integrations, Application management and Consulting services like GAMP5 Compliance, Data Security and GDPR Compliance, MedDRA & Drug Coding, Regulatory submission & Partner distribution rule implementation, Regulatory Audit support and Application performance tuning services.

Our Vision: Simplify Regulatory Compliance for the Life science industry.

Our Core Values:
– Open Culture.
– Build for a purpose.
– Be the change you seek.
– Stay Humble.
– Customer Delight.

MAIN5 is a premier consulting firm dedicated to the life sciences industry. We specialize in enhancing operational efficiency, ensuring regulatory compliance, and driving digital transformation. With deep expertise in pharmaceuticals, biotechnology, medical devices, and healthcare technology, we offer tailored solutions across regulatory affairs, data governance, quality management, and systems validation.

At MAIN5, we redefine consulting with a dynamic and forward-thinking approach: We stand for unparalleled expertise, tailor-made solutions and partnership-based collaboration. Our team of over 60 professionals, including regulatory experts, digital transformation specialists, and operational efficiency mavens, collaborates closely with clients to foster innovation and drive digital transformation.

Choosing MAIN5 means embarking on a journey towards strategic growth, operational excellence, and regulatory compliance, guided by a partner renowned for its industry expertise, customized solutions, and proven success. With our unwavering commitment to the success of our clients, we guide Life Sciences organizations towards achieving their most ambitious goals.

Together, let’s drive digital transformation in Life Sciences.

NNIT is a leading provider of IT solutions to life sciences internationally, and to the public and private sectors in Denmark.

We focus on high complexity industries and thrive in environments where regulatory demands and complexity are high.

We advise and build sustainable digital solutions that work for the patients, citizens, employees, end users or customers.

We strive to build unmatched excellence in the industries we serve, and we use our domain expertise to represent a business first approach – strongly supported by a selection of partner technologies, but always driven by business needs rather than technology.

NNIT consists of parent company NNIT A/S and group company SCALES. Together, these companies employ more than 1,700 people in Europe, Asia and USA.

Read more at www.nnit.com

ProductLife Group (PLG) is a global Life Sciences consultancy supporting pharma, biotech, and medtech companies throughout the full product lifecycle.

We aim to improve patient access to safe, effective healthcare solutions by delivering consulting and outsourcing services across development, launch, and post-market phases.

Within PLG, our Consulting & Digital department is a dedicated Veeva Center of Excellence, guiding clients on their digital transformation journey with Veeva Vault.

We support all phases, including business consulting, implementation project delivery, change management & training, migration, validation, and post-implementation support.

Our certified consultants combine deep Veeva expertise with regulatory and operational knowledge to ensure every solution is tailored, compliant, and aligned with business needs.

With 20+ years of experience, 1,000+ clients, and presence in 150+ countries, PLG is a trusted partner in GxP-compliant transformation—committed to long-term partnership, innovation, flexibility, and continuously delivering value.

As the leading advisor to organizations across the health continuum, PwC plays a critical role in helping clients solve an array of emerging complex problems facing manufacturers, service providers, and new market entrants. We have invested in developing strategy, operational, commercial, and clinical expertise.

Spotline is a trusted Veeva Product, Services, and AI Partner supporting life sciences organizations worldwide. We help companies streamline Veeva operations, reduce compliance risk, and maximize business value across both GxP and non-GxP environments. With certified solutions and experienced global teams, Spotline enables faster transformation and long-term success across the entire Veeva ecosystem.

Spotline offers two certified products designed to help life sciences organizations stay compliant, efficient, and inspection-ready:

• V-Assure is an automated testing platform purpose-built for Veeva Vault. It simplifies validation, accelerates release cycles, and supports testing of third-party integrations and Veeva Validation Management—reducing manual effort and ensuring continuous audit readiness.
• V-Assist is an AI-powered digital assistant embedded within Vault. Designed for R&D and business teams, it provides real-time, contextual guidance to help users navigate complex processes, improve productivity, minimize errors, and reduce dependency on IT support.

Spotline is a dedicated services partner for life sciences delivering comprehensive professional services across the Development Cloud, Quality Cloud, and even Commercial Cloud. Our global delivery model is backed by certified Veeva experts across multiple domains.

With a strong track record supporting both fast-growing biotechs and global pharmaceutical enterprises, Spotline offers scalable services and modern tools to help clients meet regulatory requirements, improve operational agility, and drive measurable outcomes from their Veeva investments.

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

We bring together a talented team of professionals, who work globally, with a deep understanding of patient and physician behaviors and market dynamics. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients.

Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.

To learn more about how we are Shortening the distance from lab to life®, visit syneoshealth.com.

Tata Consultancy Services (TCS) is a digital transformation and technology partner of choice for industry-leading organizations worldwide. Since its inception in 1968, TCS has upheld the highest standards of innovation, engineering excellence, and customer service.

Rooted in the heritage of the Tata Group, TCS is focused on creating long term value for its clients, investors, employees, and the community. With 607,000+ highly skilled consultants in 55 countries and 180 service delivery centres across the world, TCS has been recognized as a top employer in six continents. With the ability to rapidly apply and scale new technologies, TCS has built long term partnerships with its clients – helping them emerge as perpetually adaptive enterprises. Many of these relationships have endured into decades and navigated every technology cycle, from mainframes in the 1970s to Artificial Intelligence today. TCS generated consolidated revenues of US $30 billion in the fiscal year ended March 31, 2025.

Zifo is the leading global enabler of AI and data driven enterprise informatics for science driven organizations. With extensive solutions and services expertise spanning research, development, manufacturing, and clinical domains, we serve a diverse range of industries, including Pharma, Biotech, Chemicals, Food and Beverage, Oil & Gas, and FMCG. Trusted by over 190 science-focused organizations worldwide, Zifo is the partner of choice for advancing digital scientific innovation.

At Bright Affect, we specialise in learning and technology adoption, with deep expertise in Veeva Vault. We help life sciences organisations get more from their systems by supporting not just the technology, but also the processes and content that make it work in the real world.

Our practical, experience-led approach gives people the understanding and confidence to use new tools effectively – not just knowing how to use them, but why they matter. By aligning learning with real tasks and roles, we improve engagement, increase utilisation, and drive long-term value from your technology investment.

DAQUMA is a Copenhagen based consulting company, providing project consulting, data migration- and AI services to the life sciences industry. We deliver services across Clinical, Quality, Regulatory Affairs and Commercial.

3x certified Veeva partner for 1) Development Cloud, 2) Data migration, and 3) AI Partner.

Our 40 consultants deliver projects across 20+ global life sciences companies, we pride ourselves on delivering results through professional execution, transparent collaboration, and a focus on value.

Deloitte provides industry-leading audit and assurance, tax and legal, consulting, financial advisory, and risk advisory services to nearly 90% of the Fortune Global 500® and thousands of private companies. Legal advisory services in Germany are provided by Deloitte Legal. Our people deliver measurable and lasting results that help reinforce public trust in capital markets, enable clients to transform and thrive, and lead the way toward a stronger economy, a more equitable society and a sustainable world. Building on its 175-plus year history, Deloitte spans more than 150 countries and territories. Learn how Deloitte’s approximately 457,000 people worldwide make an impact that matters​ at www.deloitte.com/de​.

ELIQUENT Life Sciences is a leading consulting group delivering the regulatory, quality, and safety solutions that global life sciences innovators need to gain and maintain market authorization for their products.

Our unprecedented assembly of regulatory leaders, industry experts, and technical specialists support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.

Together, we bring clarity to regulatory complexity with integrated solutions and a full-service approach that unlock success and clear the path to better health. Learn more at ELIQUENT.com

Celebrating 20 years, LPW Training is a global leader in Pharmaceuticals and Life Sciences technology training. Our mission is to deliver innovative, engaging learning experiences that drive best-in-class adoption. As a Preferred Veeva Alliance Partner for over 15 years, our certified Trainers and Learning & Development Leaders specialize in Veeva CRM and Vault. We provide both standard and custom blended learning solutions, along with Project and Change Management services.

Known for our collaborative approach, LPW partners closely with customers to align training with business goals, creating immersive learning plans that equip teams to navigate key applications, reports, and processes effectively.

With training delivered in over 50 countries and 35+ languages, we understand the cultural, linguistic, and experiential nuances that impact learning success. Globally, LPW has the expertise, resources, and reach to help your team maximize the return on your technology investment.

Pinnaxis is a group of highly skilled individuals with specialized expertise in various Safety Systems including Veeva Safety. With our deep understanding of pharmacovigilance (PV) and regulatory requirements, we can help you streamline your safety processes, improve compliance, and enhance patient safety.

Our Veeva certified pool of resources makes us stand out and provides the best mix of Business and Technical skills required to get you onboarded to the Veeva platform. Our team of experts, combined with our tools, solutions, and accelerators, ensures a seamless and efficient implementation experience empowering your organization to optimize safety processes and achieve regulatory compliance.

Our Veeva Vault Safety Services:
– Data Migration
– Reporting
– Integration
– Testing & Validation
– Training (End User / Train-The-Trainer)
– Consulting Services (Business Process Design, Configuration, RIMs Connections etc.)
– Managed Services

Prudentia supports the implementation of Veeva Safety and SafetyDocs. We design the business process, conduct the data migration, develop the validation approach, author the test scripts, design and implement the reports, and lead the project management office.

Founded in 2012, Prudentia Group has organically grown into a trusted global partner for the pharmaceutical and medical device industries. Our team of experienced drug safety professionals delivers management and technology consulting services focused on simplifying complex challenges in clinical and post-marketing safety and surveillance.

We specialize in the implementation and optimization of safety databases, provide managed services to ensure their seamless operation, and offer innovative, turnkey applications that bridge critical gaps in leading safety systems. Our goal is to enhance patient safety through pragmatic, effective, and technology-driven solutions that align with regulatory expectations and industry best practices.

With a commitment to agility, objectivity, and quality, Prudentia empowers life sciences organizations to build safer, smarter pharmacovigilance systems across the entire product lifecycle.

SPORIFY is a reference data management system purpose-built for the life sciences industry to simplify management of controlled vocabularies and IDMP implementation. SPORIFY serves as an accelerator to provide everything an organisation needs to maintain harmonised, compliant data.

With its user-friendly interface, powerful key features, and interoperability across systems and geographies, SPORIFY supports mapping, synchronisation, and notification services for health authority data.

Yseop is the leader in Generative AI for regulated industries, reimagining the future of scientific writing to accelerate access to life-saving treatments. Its human-centric platform serves as a true “Copilot” for medical writers, streamlining the creation of high-quality regulatory documents from first draft to final submission with speed and precision.

With a suite of industry-specific applications and hybrid NLG technology—combining symbolic AI, machine learning and LLMs—Yseop transforms months of manual work into scalable, efficient processes. It accelerates clinical and regulatory documentation while ensuring compliance and eliminating time-consuming manual rework.

Yseop Copilot is the only platform that combines AI-generated text, regulatory rigor, real-time collaboration and full CTD coverage, all embedded within the tools medical writers already use. Built with a robust “human-in-the-loop” approach, Yseop ensures accuracy, expert oversight and compliance with global standards saving thousands of hours in document preparation and empowering faster drug approvals.