April 25, 2024

Success Story Roundup: Digital Transformation in Life Sciences

Life Sciences
Back to All News
Success Story Roundup: Digital Transformation in Life Sciences | Adlib Software

Adlib Success Story Roundup: Digital Transformation in Life Sciences

For life sciences companies operating in a highly regulated industry, manual and paper-based document-management processes don’t produce the speed, accuracy, and consistency needed to achieve compliance and maintain a competitive edge. Since cumbersome document-centric processes impact virtually every area of a life sciences enterprise—from operations to data security and compliance—it makes sense to bring digital transformation to every facet of these processes.

However, not all digital transformation in life sciences is truly revolutionary. To fundamentally transform their enterprises, life sciences companies must adopt all-digital document-management solutions that address universal business challenges across the entire organization versus those that deliver a temporary, superficial boost to business outcomes at best.

Keep reading to learn how leading life sciences companies are eliminating manual intervention, improving business outcomes, and achieving their digital transformation goals by enriching their critical data and documents.


Multi-Billion Euro Pharma Company Curbs Submission Errors & Rising IT Costs with Adlib 

For a leading European pharmaceutical company, managing and maintaining a suite of 20+ disparate document-conversion solutions led to significant operational challenges, erroneous FDA submissions, and costly fines and delays. With a more streamlined approach in mind, the company selected Adlib as its primary document conversion solution. This pharmaceutical organization was able to decommission 20+ rendering platforms, reduce operational costs, and significantly improve the quality and timeliness of its FDA submissions by adopting Adlib's enterprise platform.

Global Pharmaceutical Company Streamlines Internal Processes with Adlib 

For pharmaceutical companies who invest a considerable amount of time and money to developing life-saving health products, there’s no room for errors and delays during the submission process. However, for Adlib’s leading life sciences customer—one of the world's premier biopharmaceutical companies—onerous manual processes and lack of searchability meant that FDA submission documentation was produced with unreliable quality and great difficulty. This global pharmaceutical company eliminated steep fines, delays, and inflated IT costs by adopting Adlib enterprise document conversion platform.

Life Sciences Manufacturing Company Maximizes Uptime & Achieves Compliance by Automating its Document-Centric Processes

For a multinational consumer goods manufacturing division of a life sciences organization, producing and managing vast volumes of compliance documentation was stalling production times, monopolizing critical knowledge workers, and preventing the organization from reaching its digital transformation goals. The company recognized the need to automate their labor-intensive document-management processes, so they turned to Adlib. Adlib helped this enterprise increase the speed and volume of its document processing tenfold—netting $750,000+ per week in operational savings.

Leading Pharmaceutical Company Eliminates Costly Errors & Re-Submissions by Unifying its ECMs

For a global pharmaceutical company, using multiple, disparate document-management systems resulted in costly FDA submission errors and loss of valuable intellectual property (IP). For every delay and resubmission they faced, the company lost $250,000 and was delayed an additional 30-60 days—so there was a steep business costs associated with simply maintaining the status quo.

Additionally, critical files weren’t readable, and the company’s disparate suite of solutions couldn’t handle the massive volume of email sent and received on a daily basis. This enterprise was able to unify their ECMs, eliminate resubmissions, and decommission costly and insufficient solutions by implementing Adlib. 

June 25, 2024
Use case: Unifying platforms for improved efficiencies with FDA submissions
Learn More
June 1, 2024
How do I make sure my FDA submissions are compliant?
Learn More
October 16, 2023
Mastering Healthcare Documentation with the Pros: How to Transform Your Compliance, Auditing, and Legal Processes through Scanning and Document Transformation
Learn More

Schedule a workshop with our experts

Leverage the expertise of our industry experts to perform a deep-dive into your business imperatives, capabilities and desired outcomes, including business case and investment analysis.