People Value Research, Ltd.
PVR is a patient-centric Clinical Research Organization (CRO) dedicated to enhancing global health through innovative clinical research. With a focus on real-world data and agile project design, PVR aims to improve patient recruitment, engagement, and retention in clinical trials, ultimately contributing to successful market authorization of new therapies.
Industries
N/A
Products
In-house OCR and clinical document processing pipeline
A bespoke image-processing and OCR solution fine-tuned for clinical documents with confidence scoring, automated transcription, LLM-based summarization, and vector-database indexing for semantic retrieval.
In-house OCR and clinical document processing pipeline
A bespoke image-processing and OCR solution fine-tuned for clinical documents with confidence scoring, automated transcription, LLM-based summarization, and vector-database indexing for semantic retrieval.
Services
Clinical trial research and development
End-to-end clinical trial services including regulatory strategy, medical writing, project management, site management, monitoring, biostatistics, data services and pharmacovigilance.
Patient-focused services
Services to support patient engagement and retention including patient travel, at-home nursing, reimbursement coordination and direct-to-patient delivery.
Biospecimen sourcing and logistics
Retrospective and prospective human biospecimen sourcing (tissue, FFPE blocks, biofluids), project kit assembly, site training and worldwide distribution under approved protocols.
Data management and analytics
Custom secure cloud-based data management, data governance, data cleaning, normalization, statistical analysis and machine learning support for clinical datasets.
Regulatory and medical writing consulting
Preparation of regulatory documentation, submissions and medical writing deliverables to support approvals and regulatory interactions.
Pharmacovigilance and safety services
Safety data collection, handling of AE/AESI/SAE, and preparation of safety and efficacy reports for trials and post-market activities.
Clinical trial research and development
End-to-end clinical trial services including regulatory strategy, medical writing, project management, site management, monitoring, biostatistics, data services and pharmacovigilance.
Patient-focused services
Services to support patient engagement and retention including patient travel, at-home nursing, reimbursement coordination and direct-to-patient delivery.
Biospecimen sourcing and logistics
Retrospective and prospective human biospecimen sourcing (tissue, FFPE blocks, biofluids), project kit assembly, site training and worldwide distribution under approved protocols.
Data management and analytics
Custom secure cloud-based data management, data governance, data cleaning, normalization, statistical analysis and machine learning support for clinical datasets.
Regulatory and medical writing consulting
Preparation of regulatory documentation, submissions and medical writing deliverables to support approvals and regulatory interactions.
Pharmacovigilance and safety services
Safety data collection, handling of AE/AESI/SAE, and preparation of safety and efficacy reports for trials and post-market activities.
Expertise Areas
- Clinical trial management and operations
- Patient-centric trial design and retention strategies
- Real-World Data and Real-World Evidence generation
- Biospecimen collection and biorepository services
Key Technologies
- Machine learning for text and image processing
- Optical character recognition (OCR)
- Local large language model (LLM) deployment
- Vector database indexing and semantic search