QEdge

6 reviews

QEdge is an enterprise quality management software that handles change controls, deviations, market complaints, CAPA, and training records.

PharmaNET

2 reviews

Our dynamic, intuitive and user friendly distribution software for Pharmaceutical, empowers you to streamline your entire distribution channel which includes demand management, tracking lot and serial no., expiry dates, formation of contracts, risk management, receivables management and primary and secondary sales management and many more , specially built for global pharmaceutical players.

Process XE

1 review

This Digital, Smart Manufacturing process automation is principally developed for the Pharmaceutical, Manufacturing, Life science and Healthcare industries. It is easy to use for operators and offers digitization and automation of processes such as data capture, batch information exchange, batch production management, data security maintenance, data integrity and report production, ensuring compliance with cGMP requirements. This Manufacturing Execution System (MES) comprises of the following: - Weighing and Dispensing System (WDMS) - Electronic Batch Manufacturing Records (eBMR) - Equipment Logbooks (eLogbook) - CPP/ CPV - Device Decoder

PvEdge

1 review

This is a trusted industry-ready, cloud-based Pharmacovigilance and Safety Database software. It is pre-validated and is quick to implement, providing faster ROI with the added benefit of data migration. What PvEdge offers: 1. Manage Drug, Device, Vaccines & Combinational Products' Core Case Processing with ICSR Gateway Submission 2. Product Inquiry (MICC Tool) 3. Literature Surveillance 4. Triage Management 5. Specialised for Human & Veterinary Vigilance 6. Safety Data Exchange Agreement System (SDEAs) 7. Pharmacovigilance Quality Management 8. eCTD Publishing - PADER/ PSUR

FFReporting Pharmaceuticals

1 review

FFReporting Sales Force Automation (SFA) provides various features which also helps to propel your business.

FForce

0 reviews

FForce, an AI-powered Sales Force Automation solution, is designed to boost sales efficiency and improve customer engagement. It helps sales teams by automating routine tasks, providing tools like eDetailing for presentations, and offering real-time analytics for informed decision-making. By streamlining workflows and providing valuable insights, FForce allows sales professionals to focus on building customer relationships and closing deals, ultimately enhancing sales productivity and customer retention.

BizNET

0 reviews

Sarjen offers three specialized solutions for clinical trial management and lab automation. The Early Phase CTMS (BizNET) and Late Phase CTMS (Smart Trial Suite) are clinical trial management systems that streamline and automate early and late-phase trials, respectively. They ensure compliance, enhance data integrity, and reduce operational costs through features like intelligent automation and seamless integration. The Bioanalytical LIMS is a lab information management system that automates workflows for bioanalytical labs, ensuring data integrity, compliance with standards like 21 CFR Part 11 and GLP, and improving overall productivity and turnaround times. Together, these solutions provide a comprehensive suite for clinical research and lab operations.

KnowledgeNET

0 reviews

Sarjen's Global Dossier Publishing Software is a solution designed to simplify and automate dossier management and submission processes. It uses tailored, automated workflows to streamline the creation, validation, and submission of regulatory dossiers for specific regions and regulatory authorities. The software helps to achieve faster regulatory approvals, reduce manual errors, and ensure data consistency, ultimately improving operational efficiency and producing audit-ready documentation. It includes features like real-time tracking, version control, and compliance support for standards like FDA and EU.

Sarjen's RIMS

0 reviews

Sarjen's RIMS (Regulatory Information Management System) is a centralized, IDMP-compliant platform that streamlines and automates regulatory processes for the life sciences industry. The solution uses intuitive workflows to efficiently track data, ensuring global compliance. By centralizing regulatory data, RIMS allows for easy tracking of submissions, approvals, variations, and renewals, which improves overall efficiency and reduces manual errors. The system helps manage the entire product lifecycle from registration to approval and supports data-driven decision-making, leading to faster go-to-market timelines and reduced operational costs.