Catalyzing Digital Transformation in Life Sciences

Catalyzing Digital Transformation
in Life Sciences

For life sciences and pharmaceutical companies that invest a significant amount of time and money to developing life-saving health products, there’s no room for errors and delays. Yet, many organizations rely on labour-intensive document-management practices that introduce errors, stall critical workflows, and prevent them from producing submission-ready PDF/A assets in a timely and accurate manner. To support enterprise-wide digital transformation, life sciences and pharma companies must enrich their data and automate their manual and paper-centric document-management processes.

Eliminate Costly Errors & Delays, Manage Critical Documentation & Automatically Produce Submission-Ready PDF/A Assets.

Accurate Compliance-Friendly Data: The DNA of Digital Transformation

Adlib allows life sciences organizations to enrich data and prepare it for successful evaluation, auditing, sharing, and long-term digital preservation—curbing costly errors and delays and facilitating enterprise-wide digital transformation.

DATA CAPTURE
Ingests and enriches large volumes of unstructured data from various sources to transform business-critical documents into actionable, compliance-friendly data.
DOCUMENT
CONVERSION

Enterprise document-to-PDF capabilities automatically convert content into text-searchable, FDA and EMA-compliant PDF/A documents for LTDP and document classification. The identical format, layout, and content of the original documents is left intact.

ACCURATE COMPLIANCE-FRIENDLY DATA

PROGRESSIVE CLASSIFICATION
Advanced text analysis and intelligent data identification are leveraged to classify document types and extract relevant metadata. Based on the information, documents are automatically routed into the appropriate workflows, analytics engines, and/or repositories.

€15.9 Billion Pharma Company Curbs Submission Errors & Rising IT Costs with Adlib Enterprise

Read how a leading European pharmaceutical company was able to decommission 20+ rendering platforms and significantly improve the quality and timeliness of its FDA submissions by adopting Adlib Enterprise.

Digital Transformation in Life Sciences

Scott Mackey, Adlib VP of Customer Success, discusses how life sciences organizations can meet regulatory standards and accelerate time-to-market by automatically capturing, standardizing, extracting, and leveraging critical data.

Fortune 100 Pharmaceutical Company Recoups $1.7 Million in Licensing,
Support & IT Costs by Upgrading to Adlib Enterprise

THE BUSINESS CHALLENGES
For a Fortune 100 pharmaceutical company, cumbersome manual workflows and lack of searchability meant that FDA submission documentation was generated with great difficulty and unreliable quality.
THE CONTENT NEEDS
In order to generate FDA submissions in a timely and accurate manner, the pharmaceutical company needed an enterprise-grade solution that would allow them to consolidate their systems and combine and reformat their content.
THE ADLIB SOLUTION
After upgrading to Adlib Enterprise, the company was able to automate its document-management workflows, greatly improve the accuracy and timeliness of submissions, curb rising IT costs, and accelerate its time-to-market.

WEBINAR: Enrich Data & Protect Your Research

Learn how “improving and moving” critical documentation can help you avoid data duplication, accelerate and automate the FDA submission process, ensure compliance, and protect IP and other sensitive information.

Success Stories

Life Sciences Manufacturing Documentation Automated to Maximize Up-Time & Achieve Compliance

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Respiratory Care Products Designer & Manufacturer Streamlines PDF Conversions + Simplifies Compliance
Respiratory Care Products Designer & Manufacturer Streamlines PDF Conversions + Simplifies Compliance

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Global Pharmaceutical Company Leverages Adlib to Unify ECMs & Eliminate Costly Errors & FDA Resubmissions
Global Pharmaceutical Company Leverages Adlib to Unify ECMs & Eliminate Costly Errors & FDA Resubmissions

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Medical Device Manufacturer Automates Enhancements & Improves Compliance
Medical Device Manufacturer Automates Enhancements & Improves Compliance

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Additional Life Sciences Resources

Learn how life sciences organizations are improving the efficiency of document lifecycle workflows by integrating document conversion and archiving technology into Enterprise Content Management (ECM), Product Lifecycle Management (PLM), and other business applications.
Success Story Roundup: Digital Transformation in Life Sciences (Article)
Discover how premier life sciences companies are improving business outcomes, eliminating manual workflows, and achieving their digital transformation goals by enriching their critical data and documents.
Capture for Insurance (Solutions Brief)
Learn how Adlib can empower your organization to solve the 5 most common document challenges life sciences companies face.
Looking for an enterprise-grade document-to-PDF solution for your pharmaceutical, biotechnology, or medical device organization? Follow these best practices to ensure the right fit.
Read this third-party report to learn how Adlib supports the Electronic Common Technical Document Submissions Preparation (eCTD) validation specifications required by the FDA.
Explore how leading life sciences firms are expediting the submission process, reducing submission costs and duration, and speeding time-to-market by automatically generating FDA-ready PDFs.