Accenture Life Sciences Cloud For R&D
The industry platform for running clinical trials that deliver better patient outcomes
A Single
Version Of
the Truth
Accenture Life Sciences Cloud for R&D (ALSC) helps companies run faster clinical trials with better transparency and easy access to trial information so you can make smarter strategic decisions.
See how the Accenture Life Sciences Cloud can revolutionize your clinical trials
Built For
the Industry... With
the Industry
through a collaboration with our Life Sciences Cloud Coalition comprised of global industry leaders working together to transform R&D and deliver better outcomes.
Check out how Pfizer, Merck, Vertex, and GSK are revolutionizing R&D.
The Challenge
The Future Is Now: Transforming Clinical Trials
Accessible Knowledge
Find, exchange and reuse your organization’s expertise and memory
Liquid Workforce
Collaborate with your workforce and partners with agility and flexibly aligned to a common set of goals
Digital Trust
Have confidence in your people and processes with data, information and documents enabled by a single source of truth
Intelligent Automation
Operate in ways you’ve never imagined with your people, digital solutions and services
Predictable Disruption
Embed innovation with line of sight to success enabled by a flexible platform
-
The Solution
Working Together For Better Outcomes
Our Life Sciences Cloud Coalition brings together like-minded leaders to drive innovation and digitally-enable R&D to speed drug development and improve quality—sharing experience, contribution and risk.
THE POWER OF COLLABORATION:
Listen to R&D leaders talk about transforming the industry.
-
The Solution
use clinical data in ways never before imagined
Realizing Clinical Portfolio Strategy
Provides you with the freedom to think about your strategic goals by enabling the intelligent management of your clinical portfolio and the agility to make quick adjustments as needed
Sustaining Regulatory Compliance and Inspection Readiness
Provides confidence in your organizations inspection readiness by transforming the end-to-end metadata process while providing confidence in data lineage
Executing Clinical Studies
Creates the ability to oversee and manage the execution of your clinical studies in ways never imagined impossible, through increased transparency and access to information
Optimizing Business Partner Collaboration
Impacts all areas of business by transforming how resources interact, consume information, collaborate, and work
Enabling M&A Activity
Facilitates seamless and rapid consumption of information resulting from external activity without completing full integrations
What’s Inside
-
Accenture’s Life Sciences Cloud for R&D features five core modules that enable your organization
to capture, store, import and standardize diverse and complex internal and external data types that continue to grow in volume. With this capability, our clients are able to compare and contrast data that was previously never comparable and unlock information about their products and operations never known before.
-
The Clinical & Scientific Data Warehouse (CSDW) delivers a platform to aggregate data for analysis.
CSDW provides the business an aggregated view of both internal and external data, conformed to industry standards, in a fully validated, high-performance environment. Enforces and tracks standards across data from multiple systems and enables data standardization for cross-study analysis.
-
The Analysis & Reporting Workbench (ARW) provides a flexible statistical analysis environment that audits traceability between data, programs, and outputs.
ARW is the powerful tool for planning and developing outputs within a controlled validation cycle. It defines the analysis components that can be tracked and re-used across multiple studies and programs, enabling validated programs and report structure well before database lock.
-
The Metadata Registry (MDR) enables industry standards management and creation of study specifications based on approved standards.
MDR provides Clinical Data Standards Metadata to ensure submission of CDISC-compliant clinical data to Health Authorities. It includes structure and attributes to extend standards for Study Usage for ADaM, Controlled Terminology, Data Acquisition, Data Review Model, Data Verification, SDTM, TFL, Transformation/Mapping, VLM standards.
-
The Unstructured Content Repository (UCR) provides a central storage location creating a single source of truth for all ALSC content.
UCR is the cloud storage location of all ALSC content with full indexing providing robust content search capabilities. It allows business users to quickly and efficiently store, retrieve, and re-use content across the platform for a myriad of clinical processes and operations.
-
The Clinical Operations Insights Platform (COIP) enables delivery of the right information, at the right time, to the right team member
COIP is the trifecta of operational data-warehousing, analytics and machine learning engines in one. It helps reduce “Time to Decision” and gain deeper insights on Trial Operations data enabling operations teams to run in an agile manner to proactively act on potential risks as well as effectively manage day to day Clinical Trial operations.
Who We Work With
-
Clinical Aggregation Layer Created
Confidence in data and information with a single source of truth.
Ability to seamlessly track and manage thousands of studies with the push of a button.
Enablement of a new partner operating model and an engine for sustainable innovation.
-
Patient Data Simplified
Simplified access to patient data and study information.
Streamlined processes and documentation that reduce workarounds and inefficiencies.
Accelerated cycle times in study start-up and backend data management processes.
Enhanced quality built into architecture, study design, standards, processes and documentation.
-
Clinical Collaboration Optimized
Seamless integration with data standards management processes.
Improved collaboration on patient and study information.
Enhanced processes increasing business efficiency.
Robust quality measures ensuring regulatory compliance and inspection readiness.
What We Think
Geoff Schmidt
Managing Director -
Life Sciences, Global Technology Lead
Geoff Schmidt is a managing director and global technology lead in Accenture’s Life Sciences practice. Geoff has been with Accenture since 1996 and has spent his entire career working with Life Sciences clients. He initially specialized in architecting, implementing and running global application development and maintenance organizations and since then has held roles of increasing responsibility in Sales, Client Account Leadership, as well as leading Accenture’s global R&D Technology business.
He has Bachelor degrees in Management and Computer Science from State University of New York (SUNY) Geneseo, and lives in the Philadelphia suburbs with his two children.
Michel Rider
Managing Director -
Life Sciences, R&D
Michel is a managing director of product strategy for the Accenture Life Sciences Cloud platform, responsible for driving the product vision and roadmap. With a diverse range of experience, Michel has delivered a number of roles across the Life Sciences R&D value chain both prior to and during her time with Accenture. She has experience as a scientist, business analyst and project manager.
Connect With Us
LIFE SCIENCES BLOG
Accenture’s life sciences experts share their insights and opinions on the pharmaceutical, biotechnology, medical technology, and consumer health industries.
Accenture’s life sciences experts share their insights and opinions on the pharmaceutical, biotechnology, medical technology, and consumer health industries.
Stay In The Know
Receive e-mails from Accenture featuring new content that matches your interests.
Visit the subscription center to make your selections and subscribe to New from Accenture.