Foxit PDF SDK Solutions for Pharmaceuticals
Errors in manufacturing pharmaceuticals can cost lives. To guard against such errors and ensure a transparent paper trail, pharmaceutical regulatory agencies have some of the most rigorous and strict documentation requirements of any industry in the world. Whether moving from paper records or from legacy document management software, PDF technology allows companies to manipulate and control their documentation processes more powerfully than ever.
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Import Legacy Paperwork to Modern Databases
Pharmaceutical manufacturers are required to hold documentation for every stage of production, from the receipt of the raw materials, through the manufacturing procedures, to storage and transport. Testing is required at each stage and results must be held on file for years in case of a complaint or recall. Due to the long timelines involved with retaining documents, many pharmaceutical companies even now are working with a mix of old paper records as well as electronic documents, or need to add paper documentation to their document management system on a daily basis. Using an OCR reader tool, which comes packaged into many PDF SDKs, makes digitally recording old and new paper documents easy. Digital documentation makes searching record databases much easier. With OCR reader tools, any paper record can instantly be pulled up in a simple text search.
Comply with Regulatory Requirements
The FDA and eCTD requirements for pharmaceutical documents can be found here, and cover many aspects of document minutiae such as images, formatting and optimization for fast viewing. Foxit PDF solutions come with the tools needed to submit compliant documents, without the need for additional software. By building in-house applications to manage PDFs, compliance checks can be automated to quickly flag non-compliant documents. While any document management system solves the issue of backing up and preventing physical damage to the records, PDF technology allows companies to automatically save documents in PDF-A format. The records are readily available and organized to show to regulatory auditors upon request in the preferred format for long term storage.
Streamline Processes with Many Stakeholders
With such extensive record keeping, pharmaceutical documents can have dozens of different stakeholders. A huge cause of lost productivity is time lost in transit between stakeholders; one manager being away for the week can cause a backlog of documentation. Moving from paper records and physical file storage to a fully digital documentation system offers hundreds of ways to streamline these complex processes. While document management systems are a great solution to begin with, many companies find they need more power and flexibility than off-the-shelf systems provide. With a PDF SDK, developers can create sophisticated internal applications where the mundane steps are automated. Steps can be built into workflows to automatically to check documents for regulatory compliance. Knowing where and to who each document needs to be sent, in what order, with automatic filing and back ups, cuts the time lost between each stakeholder exponentially. Signatures and certifications are entered directly on the electronic document. This input can be done from any device – a phone, tablet, or workstation, also cutting waiting times between steps.
Keep Sensitive Information Secure
Security is another major concern for the pharmaceutical industry. Manufacturing often uses trade secret or proprietary information which need to be kept confidential. Paper records have clear security issues, and even controls for digital documentation can fall way short of the mark. Investing in PDF technology gives a company sophisticated methods to keep their documentation secure. From password protecting sensitive documents, to restricting access to certain users, to limiting where and when a document can be edited, downloaded or shared, among others. With so much at stake if errors are made, ensuring the correct person signs off each process is paramount. Standard signatures are vulnerable to forgery. Digital signatures can be embedded into documents with PDF technology, and digital signature verification used to confirm them. Foxit PDF SDK arms developers with the tools to develop enterprise-class PDF applications that fulfill all the needs of a modernizing pharmaceutical sector. Chosen by Google to be the underpinning technology for their open-source PDF engine for its versatility and power, it is the chosen PDF solution for major pharmaceutical companies such as Pfizer and Bayer.
The Important Choice
Key Benefits
Built-in Tools for Regulatory Compliance
Streamlined and Automated Processes and Workflows
World-Class Security Features
All-In-One PDF Editing Tools
100% Edge Case Success Rate
Developer Support at Every Step
Why Choose Foxit for Your Business?
Enterprise-Grade PDF SDK Solution
Foxit PDF SDK leverages Foxit’s established PDF expertise to help you provide reliable, high-quality document services trusted worldwide.
Dedicated Support Across the Globe
Foxit provides worldwide support to ensure responsive and effective assistance, accelerating your project’s success.
Developer-Friendly PDF SDK for Rapid Integration
Foxit PDF SDK offers seamless integration for developers through intuitive APIs and comprehensive documentation, allowing for quick implementation in your software projects.
Robust Performance You Can Count On
Foxit PDF SDK offers reliable document processing and rendering with a focus on speed and stability for mission-critical workflows.
Complete PDF Feature Set
Foxit PDF SDK delivers a full range of PDF capabilities—including viewing, annotation, editing, signing, OCR, and conversion—providing everything essential to meet today’s enterprise requirements.
Multi-Platform PDF Integration
Foxit’s powerful PDF SDK libraries enable developers to seamlessly incorporate advanced PDF features into desktop, mobile, and cloud applications across a variety of popular pr ogramming languages and frameworks.
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