Transform your documentation processes with our advanced, compliance-focused solution designed specifically for pharmaceutical, biotech, and regulated industries.
Explore DMS FeaturesOur comprehensive Document Management System is designed to address the unique challenges faced by life sciences organizations, ensuring compliance while improving efficiency.
Manage the complete document lifecycle from creation to obsoletion with automated workflows that ensure proper approvals and seamless transitions between document states.
Maintain comprehensive version history with automatic tracking of all changes, ensuring you always have access to previous versions while maintaining compliance with regulatory requirements.
Easily perform side-by-side comparisons between document versions to quickly identify changes, ensuring accuracy and consistency throughout the review and approval process.
Protect sensitive data from unauthorized access with role-based permissions and advanced encryption, meeting the strictest security standards for regulated industries.
Monitor document status in real-time with automatic notifications and reminders, reducing delays and ensuring timely completion of critical document-related tasks.
Connect with Learning Management Systems and other enterprise applications to automatically trigger training needs upon document updates and streamline your overall workflow.
Why traditional methods are no longer enough?
In today's fast-paced digital environment, outdated document processes create bottlenecks that impact productivity, security, and collaboration. Modern businesses need robust solutions to stay competitive.
Scattered files across devices and platforms waste valuable time and cause confusion among team members.
Multiple versions of the same document often lead to errors, conflicts, and duplicated work efforts.
Inability to define granular permissions can lead to unauthorized edits or potential data leaks.
Failure to meet industry regulations due to missing audit trails or inconsistent record-keeping practices.
Weak encryption standards and poor backup practices leave sensitive documents vulnerable to breaches.
Relying on paper-based or email-based approval processes is time-consuming and highly error-prone.
Our Document Management System addresses the key challenges faced by life sciences companies, transforming cumbersome manual processes into streamlined digital workflows while ensuring regulatory compliance.
With our solution, you can eliminate version control issues, prevent misplaced files, reduce compliance risks, and avoid costly delays that often result from inefficient document management processes.
Meet strict regulatory requirements including 21 CFR Part 11 and EU Annex 11 with comprehensive audit trails and electronic signatures.
Reduce document processing time by up to 70% with automated workflows and intelligent routing.
Eliminate paper-based processes and significantly reduce administrative overhead while minimizing the risk of costly compliance violations.
Enable seamless collaboration across departments and locations with centralized document access and real-time updates.
Work smarter with tools you already use
Easily connect to your Microsoft 365 account to store, retrieve, and manage documents within a secure cloud environment — all from within DocuSync.
Assign roles and permissions directly through your Microsoft account, ensuring only the right people can view or edit your documents in real time.
Eliminate the hassle of managing files locally. With Microsoft 365 integration, your documents are always accessible, backed up, and synced across devices.
Our Document Management System is designed to meet the most stringent regulatory requirements worldwide, ensuring your operations remain compliant regardless of location.
Experience how DocuSync can revolutionize your documentation processes, ensure regulatory compliance, and improve overall efficiency in your organization.
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