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Leverage information for innovation and profitability
Life sciences and healthcare organizations face tremendous pressure to reduce product cycle times and costs while supporting regulatory mandates. As a result, companies are seeking more efficient and secure ways to accelerate product development, promote regulatory compliance, and improve patient care delivery. Adobe can help.
Customer success stories
Procter & Gamble
A leading consumer goods manufacturer streamlines and enhances the security of research and development processes with Adobe® LiveCycle® ES solutions.
U.S. Food and Drug Administration Center for Biologics Evaluation and Research
FDA/CBER moves to electronic document submissions to streamline the review and processing of biologics research information.
Merck KGaA
Merck KGaA Deutschland deploys Adobe solutions to optimize clinical trials for new pharmaceuticals.
Roche Products Pty Limited
For Roche, the most important benefit of Adobe solutions is the ability to quickly and reliably produce quality customer-facing documents that can be delivered on paper or electronically.
Adobe and Accenture develop enterprise portal for MHRA
MHRA in the United Kingdom uses Adobe solutions to automate and improve form processes and streamline regulatory approvals.
SmartPath, Inc.
Pharmaceutical company SmartPath, Inc., speeds the review and approval of marketing documents for new treatments and enhances employee collaboration with Adobe Acrobat® software and PDF.
St. Vincent's Hospital
A leading hospital deploys Adobe solutions to improve patient care and contain costs across its extended enterprise.
Solutions
Electronic forms for product development
Discover how to transform paper processes into automated electronic data capture workflows to reduce the development time in bringing a new product to market.
Electronic submissions
Streamline the secure and auditable creation, review, approval, assembly, and delivery of regulatory submissions.
Secure information exchange
Enable a more secure movement of authenticated information and establish enforceable, auditable electronic documents of record.
Health information and collaboration
Improve processes and increase collaboration to support electronic medical records and personal health records.
Highlights
Adobe products and 21 CFR Part 11 compliance
Laws and regulations that govern the use of electronic signature technology vary worldwide by country and purpose. In the United States, the Food and Drug Administration (FDA) has issued the Guidance for Industry Part 11, Electronic Records; Electronic Signatures — Scope and Application to clarify the requirements for life sciences companies using electronic records and electronic signatures. The challenge for many companies is ensuring Part 11 compliance while simultaneously reducing the cost of product development. Adobe technology provides a scalable, unified platform that blends electronic forms, process management, security, audit trails, digital signatures, and document generation. Adobe LiveCycle ES and the Adobe Acrobat product family can help life sciences companies create and deliver rich and engaging applications that reduce paperwork, decrease costs, and shorten time to market while helping manage compliance with regulatory requirements such as CFR Part 11.
Related products
Adobe LiveCycle ES
Automate critical processes within and extend them outside your organization without requiring a major technology overhaul.
Adobe Acrobat 9
Share information and collaborate more securely using Adobe Acrobat 9 software and PDF, the standard for electronic document exchange.
Adobe Acrobat Connect Pro
Allow anyone, anywhere to collaborate on projects, conduct meetings, and deliver training in real time with Adobe Acrobat Connect™ Pro software.
