logo WEP Clinical | Treatment Access Solutions | With Every Patient
  • Company

    AT WEP CLINICAL, WE ARE WITH EVERY PATIENT

    We are a Pharmaceutical Services Provider that specializes in Drug Development Programs, Treatment Access Solutions and Market Access and Commercialization

    • About Us
    • Leadership Team
    • Global Coverage
    • Partnerships
    • Testimonials
    • Careers
  • CRO Services

    WEP CRO Built for Biotech

    We are experienced in Phase I – IV trial delivery with proven track record of excellence supporting 60+ clinical programmes worldwide.

    • Research Objectives
    • Study Protocol
    • Funding & Resources
    • Regulatory & Ethics Approval
    • Country Selection
    • Feasibility & Site Selection
    • Planning and Preparation
    • Site Set-Up & Contracting
    • Vendor Selection
    • IRT
    • Drug Supply Management
    • Data Management Planning
    • Safety Management Planning
    • Medical Monitoring Planning
    • Site Training
    • Pre-Trial Site Visit
    • Study Startup
    • Patient Identification
    • Screening & Enrollollment
    • Site Support & Management
    • Patient Retention Strategies
    • Patient Concierge Service
    • Nursing Services
    • Patient Recruitment & Retention
    • Project Management
    • Site Monitoring
    • Drug Safety & Pharmacovigilance
    • Medical Monitoring
    • Quality Control and Assurance
    • Medical Affairs
    • Medical Writing
    • Regulatory Affairs
    • Clinical Support services
    • Mobile Nursing Solutions
    • Data Cleaning & Validation
    • Statistical Analysis
    • Data Compliance & Submission
    • Data Management
    • Data Management & Analysis
    • Close-Out Site Visits and Audits
    • Final Report Submission
    • Clinical Trial Publications
    • Post-Marketing Surveillance
    • Study Close Out & Reporting

    WEP CRO Built for Biotech

    We are experienced in Phase I – IV trial delivery with proven track record of excellence supporting 60+ clinical programmes worldwide.

    • Planning and Preparation
      • Research Objectives
      • Study Protocol
      • Funding & Resources
      • Regulatory & Ethic Approval
      • Country Selection
      • Feasibility & Site Selection
    • Study Startup
      • Site Set-Up & Contracting
      • Vendor Selection
      • IRT
      • Drug Supply Management
      • Data Management Planning
      • Safety Management Planning
      • Medical Monitoring Planning
      • Site Training
      • Pre-Trial Site Visit
    • Patient Recruitment & Retention
      • Patient Identifiacation
      • Screening & Enrollment
      • Site Support & Management
      • Patient Retention strategies
      • Patient Concierge Service
      • Nursing Services
    • Clinical Support Services
      • Project Management
      • Site Monitoring
      • Drug safety & Pharmacovigilance
      • Medical Monitoring
      • Quality Control and Assurance
      • Medical Affairs
      • Medical Writing
      • Regulatory Affairs
    • Mobile Nursing Solutions
    • Biometrics
      • Data Cleaning & Validation
      • Statistical Analysis
      • Drug Compliance & Submission
      • Data Management
    • Study Closeout & Reporting
      • Close-Out Site Visits and Audits
      • Final Report Submission
      • Clinical Trial Publications
      • Post-Marketing Surveillance
    • Planning and Preparation
      • Research Objectives
      • Study Protocol
      • Funding & Resources
      • Regulatory & Ethic Approval
      • Country Selection
      • Feasibility & Site Selection
    • Study Startup
      • Site Set-Up & Contracting
      • Vendor Selection
      • IRT
      • Drug Supply Management
      • Data Management Planning
      • Safety Management Planning
      • Medical Monitoring Planning
      • Site Training
      • Pre-Trial Site Visit
    • Patient Recruitment & Retention
      • Patient Identifiacation
      • Screening & Enrollment
      • Site Support & Management
      • Patient Retention strategies
      • Patient Concierge Service
      • Nursing Services
    • Clinical Support Services
      • Project Management
      • Site Monitoring
      • Drug safety & Pharmacovigilance
      • Medical Monitoring
      • Quality Control and Assurance
      • Medical Affairs
      • Medical Writing
      • Regulatory Affairs
    • Mobile Nursing Solutions
    • Biometrics
      • Data Cleaning & Validation
      • Statistical Analysis
      • Drug Compliance & Submission
      • Data Management
    • Study Closeout & Reporting
      • Close-Out Site Visits and Audits
      • Final Report Submission
      • Clinical Trial Publications
      • Post-Marketing Surveillance
    Edit Template
  • Access Services

    Access programs With Every Patient

    Industry leader with over 16 years of experience designing and deliveing calue-driven Expanded Access (EAPs) and Post-Trial Access Programs.

    • Expanded Access Programs
    • Post-Trial Access
    • Post-Approval Named Patient
    • Market Access Solutions
    • WEP 3PL
    • Project Management
    • Real World Data
    • Pharmacovigilance
    • Advocacy
  • Therapeutic Expertise
  • WEP Insights
  • News & Media

    CASE STUDIES

    • Expanded Access
    • Post-Approval Named Patient
    • Market Access
    • Nursing Solutions
    All Case Studies

    NEWS

    • 01 Dec 2023
      WEP CLINICAL HAS PARTNERED WITH PLUSULTRA PHARMA TO SUPPLY HYFTOR® TO PATIENTS IN EU/EEA COUNTRIES (WITH THE EXCEPTION OF GERMANY)
    • 17 Jul 2023
      WEP CLINICAL ANNOUNCES PARTNERSHIP WITH GERON CORPORATION FOR AN EXPANDED ACCESS PROTOCOL FOR IMETELSTAT
    All News

    RESOURCES

    Sample Regulatory Assessment for Treatment Access Program

    View resource

    Sponsor Considerations for Post-Trial Access

    View resource
    All Resources
  • Company

    AT WEP CLINICAL, WE ARE WITH EVERY PATIENT

    We are a Pharmaceutical Services Provider that specializes in Drug Development Programs, Treatment Access Solutions and Market Access and Commercialization

    • About Us
    • Leadership Team
    • Global Coverage
    • Partnerships
    • Testimonials
    • Careers
  • CRO Services

    WEP CRO Built for Biotech

    We are experienced in Phase I – IV trial delivery with proven track record of excellence supporting 60+ clinical programmes worldwide.

    • Research Objectives
    • Study Protocol
    • Funding & Resources
    • Regulatory & Ethics Approval
    • Country Selection
    • Feasibility & Site Selection
    • Planning and Preparation
    • Site Set-Up & Contracting
    • Vendor Selection
    • IRT
    • Drug Supply Management
    • Data Management Planning
    • Safety Management Planning
    • Medical Monitoring Planning
    • Site Training
    • Pre-Trial Site Visit
    • Study Startup
    • Patient Identification
    • Screening & Enrollollment
    • Site Support & Management
    • Patient Retention Strategies
    • Patient Concierge Service
    • Nursing Services
    • Patient Recruitment & Retention
    • Project Management
    • Site Monitoring
    • Drug Safety & Pharmacovigilance
    • Medical Monitoring
    • Quality Control and Assurance
    • Medical Affairs
    • Medical Writing
    • Regulatory Affairs
    • Clinical Support services
    • Mobile Nursing Solutions
    • Data Cleaning & Validation
    • Statistical Analysis
    • Data Compliance & Submission
    • Data Management
    • Data Management & Analysis
    • Close-Out Site Visits and Audits
    • Final Report Submission
    • Clinical Trial Publications
    • Post-Marketing Surveillance
    • Study Close Out & Reporting

    WEP CRO Built for Biotech

    We are experienced in Phase I – IV trial delivery with proven track record of excellence supporting 60+ clinical programmes worldwide.

    • Planning and Preparation
      • Research Objectives
      • Study Protocol
      • Funding & Resources
      • Regulatory & Ethic Approval
      • Country Selection
      • Feasibility & Site Selection
    • Study Startup
      • Site Set-Up & Contracting
      • Vendor Selection
      • IRT
      • Drug Supply Management
      • Data Management Planning
      • Safety Management Planning
      • Medical Monitoring Planning
      • Site Training
      • Pre-Trial Site Visit
    • Patient Recruitment & Retention
      • Patient Identifiacation
      • Screening & Enrollment
      • Site Support & Management
      • Patient Retention strategies
      • Patient Concierge Service
      • Nursing Services
    • Clinical Support Services
      • Project Management
      • Site Monitoring
      • Drug safety & Pharmacovigilance
      • Medical Monitoring
      • Quality Control and Assurance
      • Medical Affairs
      • Medical Writing
      • Regulatory Affairs
    • Mobile Nursing Solutions
    • Biometrics
      • Data Cleaning & Validation
      • Statistical Analysis
      • Drug Compliance & Submission
      • Data Management
    • Study Closeout & Reporting
      • Close-Out Site Visits and Audits
      • Final Report Submission
      • Clinical Trial Publications
      • Post-Marketing Surveillance
    • Planning and Preparation
      • Research Objectives
      • Study Protocol
      • Funding & Resources
      • Regulatory & Ethic Approval
      • Country Selection
      • Feasibility & Site Selection
    • Study Startup
      • Site Set-Up & Contracting
      • Vendor Selection
      • IRT
      • Drug Supply Management
      • Data Management Planning
      • Safety Management Planning
      • Medical Monitoring Planning
      • Site Training
      • Pre-Trial Site Visit
    • Patient Recruitment & Retention
      • Patient Identifiacation
      • Screening & Enrollment
      • Site Support & Management
      • Patient Retention strategies
      • Patient Concierge Service
      • Nursing Services
    • Clinical Support Services
      • Project Management
      • Site Monitoring
      • Drug safety & Pharmacovigilance
      • Medical Monitoring
      • Quality Control and Assurance
      • Medical Affairs
      • Medical Writing
      • Regulatory Affairs
    • Mobile Nursing Solutions
    • Biometrics
      • Data Cleaning & Validation
      • Statistical Analysis
      • Drug Compliance & Submission
      • Data Management
    • Study Closeout & Reporting
      • Close-Out Site Visits and Audits
      • Final Report Submission
      • Clinical Trial Publications
      • Post-Marketing Surveillance
    Edit Template
  • Access Services

    Access programs With Every Patient

    Industry leader with over 16 years of experience designing and deliveing calue-driven Expanded Access (EAPs) and Post-Trial Access Programs.

    • Expanded Access Programs
    • Post-Trial Access
    • Post-Approval Named Patient
    • Market Access Solutions
    • WEP 3PL
    • Project Management
    • Real World Data
    • Pharmacovigilance
    • Advocacy
  • Therapeutic Expertise
  • WEP Insights
  • News & Media

    CASE STUDIES

    • Expanded Access
    • Post-Approval Named Patient
    • Market Access
    • Nursing Solutions
    All Case Studies

    NEWS

    • 01 Dec 2023
      WEP CLINICAL HAS PARTNERED WITH PLUSULTRA PHARMA TO SUPPLY HYFTOR® TO PATIENTS IN EU/EEA COUNTRIES (WITH THE EXCEPTION OF GERMANY)
    • 17 Jul 2023
      WEP CLINICAL ANNOUNCES PARTNERSHIP WITH GERON CORPORATION FOR AN EXPANDED ACCESS PROTOCOL FOR IMETELSTAT
    All News

    RESOURCES

    Sample Regulatory Assessment for Treatment Access Program

    View resource

    Sponsor Considerations for Post-Trial Access

    View resource
    All Resources
Contact us
Confirmation | Thank YouOleksandra Bystrova2024-09-11T16:48:40+01:00

Thank you for your interest in WEP!

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