Our Service Categories

Diligent’s Vendor Qualification Questionnaire templates are mapped to current regulations and span 59 clinical trial service categories.

As regulations evolve, Diligent's Vendor Qualification Questionnaire templates allow Sponsors to ensure they are asking the right questions of every Vendor they partner with. 

Developed by our team of SMEs with extensive experience conducting Vendor qualification assessments, the templates are validated against current global regulations and designed to support a rigorous, defensible qualification process.

Our 63 questionnaire templates are available through the Diligent360 and DiligentRespond platforms and span the following Vendor service categories:

Foundation

  • Business

  • Technology

  • Quality

Site-Patient

  • Investigator Site 

  • Investigator Site File 

  • Patient Recruitment & Feasibility

    • Patient Identification & Support Programs 

    • Recruitment & Retention 

  • Patient Remote Visits

  • Site Management - Site Networks 

  • Telemedicine 

  • Translation Services 

Investigational Product

  • Clinical IMP Management

  • Clinical Supply Logistics

  • Comparator Sourcing

  • Compounding 

  • Controlled Materials

  • Distribution & Warehouse Services

  • DS/DP Manufacturing 

  • General Clinical IMP (overall process oversight) 

  • Packaging & Labeling 

  • Temperature Controlled Couriers 

  • Testing & Release (incl. QP) 

Technology

  • CTMS

  • Data Hosting 

  • Digital Advertising 

  • eCOA/ePRO 

  • Electronic Data Capture 

  • Informed Consent 

  • Retention & Archival 

  • RTSM 

  • Trial Master File 

  • Wearables (All Types) 

CRO

  • Data Management

  • Decentralized Trials

  • Feasibility & Site Selection

  • General CRO

  • Investigator Site Budgets

  • Medical Writing

  • Project Management

  •  Site Monitoring - CRA

  • Statistical Programming & Biostatistics

Labs

  • Bioanalytical 

  • Biomarker 

  • Central Lab

  • ECG 

  • EEG

  • General Analytical (Release & Stability)

  • Imaging

  • Microbiology 

  • Sample Logistics & Biobanking

  • Specialty (incl. DMPK)

Safety

  • Medical Monitoring

  • Pharmacovigilance 

  •  Real World Data/Evidence

  • Safety Boards & Committees 

  • Scientific Advisory

  • Signal Detection 

Regulatory Affairs

  • HA Liaison Services

  • IND/CTA Submissions 

  • IRB 

  • Regulatory Affairs 

Foundation

  • Business

  • Technology

  • Quality

CRO

  • Data Management

  • Decentralized Trials

  • Feasibility & Site Selection

  • General CRO

  • Investigator Site Budgets

  • Medical Writing

  • Project Management

  •  Site Monitoring - CRA

  • Statistical Programming & Biostatistics

Site-Patient

  • Investigator Site 

  • Investigator Site File 

  • Patient Recruitment & Feasibility

    • Patient Identification & Support Programs 

    • Recruitment & Retention 

  • Patient Remote Visits

  • Site Management - Site Networks 

  • Telemedicine 

  • Translation Services 

Labs

  • Bioanalytical 

  • Biomarker 

  • Central Lab

  • ECG 

  • EEG

  • General Analytical (Release & Stability)

  • Imaging

  • Microbiology 

  • Sample Logistics & Biobanking

  • Specialty (incl. DMPK)

Investigational Product

  • Clinical IMP Management

  • Clinical Supply Logistics

  • Comparator Sourcing

  • Compounding 

  • Controlled Materials

  • Distribution & Warehouse Services

  • DS/DP Manufacturing 

  • General Clinical IMP (overall process oversight) 

  • Packaging & Labeling 

  • Temperature Controlled Couriers 

  • Testing & Release (incl. QP) 

Safety

  • Medical Monitoring

  • Pharmacovigilance 

  •  Real World Data/Evidence

  • Safety Boards & Committees 

  • Scientific Advisory

  • Signal Detection 

Technology

  • CTMS

  • Data Hosting 

  • Digital Advertising 

  • eCOA/ePRO 

  • Electronic Data Capture 

  • Informed Consent 

  • Retention & Archival 

  • RTSM 

  • Trial Master File 

  • Wearables (All Types) 

Regulatory Affairs

  • HA Liaison Services

  • IND/CTA Submissions 

  • IRB 

  • Regulatory Affairs 

Diligent subscribers are able to customize templates to reflect their specific protocol requirements. Our team adds new templates on an ongoing basis to reflect new Vendor qualification needs and regulatory requirements. 

Start your next trial faster with higher quality and compliance.

Our team is ready to support your unique needs. Schedule a demo today. 

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