
by Pharmasoft
Fault reporting, corrective actions, and repair tracking with root-cause analysis and compliance.
Manufacturing & Bioprocessing
by Pharmasoft
Secure electronic logbooks replacing paper with compliant audit trails for equipment operations.
Manufacturing & Bioprocessing
by Phlexglobal
Trial Master File management with AI-assisted document filing, completeness tracking, and inspection-readiness across the study lifecycle.
Clinical Trial Management
by Phlexglobal
Pre-configured Trial Master File management with AI-assisted indexing, digital document processing, and inspection-ready workflows—live in 7-10 days.
Clinical Trial Management
by Phlexglobal
Secure, compliant cloud storage for Trial Master Files after study closeout, with inspection-ready access and easy document review.
Clinical Trial Management
by Phlexglobal
Electronic Trial Master File management for CROs with inspection-ready workflows and multi-client TMF structure support.
Clinical Trial Managementby BtB Software
Laboratory information management and compliance tracking for public health, clinical, dairy, and environmental testing labs.
Lab Informatics & Operations
by Nucleics
DNA basecalling for ABI sequencers that extracts up to 50% more high-quality bases per trace.
Genomics & Omics Analysis
by Nucleics
DNA basecalling for ABI sequencers that extends read length up to 50% and reduces errors in trace data.
Genomics & Omics Analysis
by Nucleics
Basecalling and trace improvement for ABI DNA sequencers via remote processing.
Genomics & Omics Analysis
by Nucleics
DNA basecalling for ABI 377, 310, 3700, 3100, 3130, 3730 & 3500 sequencers.
Genomics & Omics Analysis
by Nucleics
Real-time quality control analysis for DNA sequencing traces, detecting nine problem types in high-throughput genomics facilities.
Genomics & Omics Analysis
by Clinion
AI-powered data capture and management for clinical trials with instant discrepancy detection, 2-week study setup, and audit-ready compliance.
Clinical Trial Management
by Clinion
AI-generated clinical trial protocols compliant with ICH M11 and TransCelerate guidelines, with real-time collaboration and audit-ready traceability.
Regulatory & Safety Documentation
by Clinion
Auto-generate ICH E3-compliant Clinical Study Reports from protocols, SAPs, and TLFs using AI, reducing manual writing by up to 70%.
Regulatory & Safety Documentation
by Clinion
Real-time patient-reported outcome collection via mobile app for clinical trials, with AI-powered validation and regulatory compliance.
Clinical Trial Management
by Clinion
Direct data capture at the point of care for clinical trials, with real-time EDC integration and full regulatory compliance.
Clinical Trial Management
by Clinion
Digital informed consent with real-time tracking, version control, and automated enrollment for clinical trials.
Clinical Trial Management
by Clinion
Centralized document management and compliance tracking for clinical trials, with DIA-aligned templates, real-time dashboards, and audit trails.
Clinical Trial Management
by Clinion
AI-powered medical image upload, de-identification, and review integrated directly into clinical trial EDC—no separate imaging system needed.
Clinical Trial Management