
Life sciences companies are under tremendous pressure to bring products to market quickly, safely, and compliantly — while building a robust pipeline and reducing research, development, sales, and marketing costs. As a result, sponsors, investigators, partners, clinical research organizations (CROs), and field sales managers are seeking more efficient, cost-effective, and secure ways to communicate and collaborate with partners, suppliers, and customers.
Adobe solutions for life sciences meet these needs, bridging the paper-to-digital divide, streamlining communications, delivering data from back-end systems and rich Internet applications to each participant in the process. Adobe solutions for life sciences combine the familiarity, security, and visual fidelity of Adobe PDF; the business logic and data exchange capabilities of XML; and rich media communications capabilities to help life sciences companies:
Learn more about key components of Adobe solutions for life sciences — Adobe PDF, Adobe Acrobat®, Macromedia® Breeze®, Adobe Reader®, and Adobe Flash® Player.
FDA/CBER moves to electronic document submissions to streamline review and processing of biologics research information.
Merck KGaA Deutschland deploys the Adobe Intelligent Document Platform to optimize clinical trials for new pharmaceuticals.
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.
MHRA in the U.K. uses the Adobe Intelligent Document Platform to automate and improve form processes and streamline regulatory approvals.
Pharmaceutical company SmartPath, Inc. speeds review and approval of marketing documents for new treatments and enhances employee collaboration with Acrobat and Adobe PDF.
Read more about Adobe's commitment to industry standards that help establish a common information-sharing infrastructure for the secure and reliable distribution and exchange of electronic documents.
Learn how Adobe supports SAFE digital signature standards to help streamline identity management.
Discover how to transform paper processes into automated digital workflows to reduce the time in bringing a new drug to market.
Join Adobe and Bio-IT World to learn how to reduce the sting of clinical development costs associated with manual, paper-based, repetitive processes.
See how Adobe helps life sciences manufacturers streamline the collaborative processes of creating, assembling, and delivering accurate, approvable electronic submissions to achieve earlier filing dates, greater accuracy and quality of data and ultimately, faster time to market.
Learn how you can reach and influence busy healthcare professionals and patients with engaging, multimedia, on-demand communications.
Create and integrate Intelligent Documents with enterprise applications and business processes.
Protect document integrity while ensuring files can be easily reviewed, commented upon, approved, and archived.
It's even more secure and easier to deploy and support. And it's packed with powerful new review and markup capabilities that help streamline the clinical trials process and bring new drugs to market faster.