Pharmaceutical

Efficiency Meets Excellence. Industry-Specific Solution

Intelligent Document Management Functionality with Graphite Studio:

Centralized Document Repository: Our Pharmaceutical Document Management System (DMS) acts as a central repository for healthcare and pharmaceutical documents, supporting regulatory filings, clinical trial data, and compliance records.
Pharmaceutical DMS Version Control and Document History: Documents undergo rigorous version control, allowing easy tracking, reversion, and complete history maintenance for regulatory compliance and traceability.
Customizable Document Metadata for Categorization and Intelligent Search Define and customize metadata fields to tag documents with relevant information, simplifying search and retrieval within our Pharmaceutical DMS
Management Document Approval Workflows: Our system supports customizable document approval workflows to ensure document review and regulatory compliance, particularly for Material Safety Data Sheet (MSDS) Management in the pharmaceutical industry.

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Real-time Compliance Monitoring: Our Pharmaceutical regulatory compliance tracking system actively monitors adherence to healthcare and pharmaceutical regulations, offering real-time insights.
Automated Notifications: The system sends automated alerts for upcoming compliance deadlines and regulatory changes. Notifications can be customized for various user roles and needs.
Audit Trail and Reporting: Maintaining a comprehensive audit trail of compliance-related activities, our system supports robust reporting. Administrators can generate compliance reports for internal and regulatory purposes.

Participant Enrollment and Tracking: Our Clinical Trial Management System (CTMS) streamlines participant enrollment, managing data, eligibility criteria, and consent forms. It tracks participant progress throughout the trial.
Data Collection and Monitoring: Simplify clinical trial data collection with standardized forms and workflows. Our Clinical Trial Management System (CTMS) system offers real-time data monitoring and quality control.
Regulatory Reporting Integration: Clinical trial managers can effortlessly generate and submit regulatory reports, customizing them to meet specific trial requirements and regulatory standards with our Pharmaceutical CTM.

Secure Patient Data Storage: Our Electronic Health Record Management (EHRM) system for pharmaceuticals provides secure storage for Electronic Health Records (EHRs) within your web application. It employs robust security measures to protect sensitive patient information.
Interoperability and Standardization: Electronic Health Records EHRs within our system adhere to standardized formats and can be securely shared with authorized healthcare providers and institutions, ensuring interoperability and compliance with healthcare standards.
Role-based Access Control: Using Graphite Studio's No Code platform, configure role-based access controls to ensure that only authorized users have access to specific patient records within our electronic health record management system.

Comprehensive Inventory Tracking: This application tracks pharmaceutical inventories down to batch numbers, expiration dates, and quantities. Users can easily check stock levels and anticipate reorder needs.
Regulatory Compliance Management: It helps pharmaceutical companies stay compliant with regulatory requirements related to inventory management, including storage conditions and recordkeeping.
Customizable Alerts and Notifications: Graphite Studio enables clients to set up customized alerts for low stock levels, ensuring timely replenishment and preventing disruptions in the supply chain.