Pharma software solutions

We can help your pharmaceutical company integrate a customized ERP system that includes specialized modules for inventory control, production scheduling, and supply chain management, all designed to meet the stringent requirements of the industry. You will enable complete traceability of raw materials through finished products, supporting both operational efficiency and regulatory compliance needs.

We develop and integrate pharmaceutical CRM systems that support the complex relationship management needs of pharmaceutical companies, from engaging with healthcare providers to interacting with regulatory agencies. The software caters to the unique sales and marketing processes of the pharmaceutical industry, including medical affairs activities and educational programs for healthcare providers.

We can help you implement supply chain management software that offers end-to-end visibility across your pharmaceutical supply chain, from sourcing raw materials to final product delivery. You'll address drug shortages through data-driven demand forecasting, inventory management, and optimization, enabling real-time supply chain visibility for proactive management of potential disruptions. At the same time, automated compliance monitoring will ensure your adherence to pharmaceutical distribution requirements.

Clinical trials are a critical part of pharmaceutical development, requiring data-driven software to manage complex study protocols and regulatory demands. We create CTMS solutions that cover the entire clinical trials process. These systems integrate with electronic data capture tools and regulatory databases, ensuring a smooth data flow throughout the clinical development journey.

We develop and integrate quality management software that provides support for pharmaceutical quality processes, ensuring adherence to quality standards across all business operations. The QMS integrates with manufacturing systems to deliver real-time quality monitoring, while automated workflows support corrective and preventive action protocols.

Post-market surveillance requires specialized software solutions that can efficiently collect, analyse, and report adverse events while ensuring compliance with global pharmacovigilance requirements. We develop pharmacovigilance software that automates various aspects of safety data management, from case intake to regulatory reporting, enabling pharmaceutical companies to maintain comprehensive safety monitoring programs.

Modern LIMS software supports all the complex analytical requirements of pharmaceutical laboratories. These systems provide comprehensive sample tracking, test results management, and quality control documentation. The software integrates with analytical instruments and quality management systems, ensuring seamless data flow and maintaining complete audit trails for all laboratory activities.

Pharmaceutical manufacturing software addresses the unique requirements of pharma production environments, from formulation management through packaging and distribution. The software provides comprehensive support for manufacturing processes, including electronic batch records, equipment monitoring, and automated quality control checks.

R&D software solutions support pharmaceutical research workflows, from early drug discovery to clinical development. The software integrates with analytical systems and databases, giving researchers easy access to critical data necessary for making informed decisions. These solutions promote collaboration among research teams while ensuring proper data security and protection of intellectual property.

EDC systems automate the collection and management of clinical data. They help the pharmaceutical sector ensure data quality while reducing the administrative burden on clinical sites. The software includes built-in data validation rules that help ensure data integrity throughout the clinical trial process.

RIM systems offer comprehensive support for regulatory submissions and interactions with authorities. These software solutions simplify the preparation of regulatory documents while helping pharma companies maintain complete audit trails and version control throughout the submission process.

EDMS solutions meet the extensive documentation needs of the pharmaceutical industry, providing secure and controlled access to critical business documents. The software supports collaborative document development while ensuring proper version control and approval workflows.

Advanced analytics capabilities enable pharmaceutical companies to extract valuable insights from their operational data. We develop BI solutions that integrate data from multiple pharmaceutical software systems, providing comprehensive dashboards and reporting capabilities that support informed strategic decision-making across all business functions.