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
    • Global Operating Model
    • Patient Centric Approach
    • Nurse Training
    • 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 delivering value-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

    Impact of U.S. Most-Favored-Nation Pricing Model on Global Product Launches & Pricing

    View resource

    Sample Regulatory Assessment for Treatment Access Program

    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
    • Global Operating Model
    • Patient Centric Approach
    • Nurse Training
    • 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 delivering value-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

    Impact of U.S. Most-Favored-Nation Pricing Model on Global Product Launches & Pricing

    View resource

    Sample Regulatory Assessment for Treatment Access Program

    View resource
    All Resources
Contact us

WEP CLINICAL EXPANDS AVAILABILITY OF XENLETA® (LEFAMULIN) NAMED PATIENT PROGRAM IN PARTNERSHIP WITH NABRIVA THERAPEUTICS

WEP Clinical (WEP) and Nabriva Therapeutics (Nabriva) are pleased to announce the expansion of the XENLETA® (lefamulin) Named Patient Program (NPP) into Australia, New Zealand, Singapore and South Africa. NPP is designed to ensure [...]

By Wep Clinical|2023-12-12T12:10:49+00:00March 25th, 2021|2021|
Read More

WEP CLINICAL EXTENDS PARTNERSHIP WITH BTG SPECIALTY PHARMACEUTICALS BY GAINING WORLDWIDE (EX-US) DISTRIBUTION RIGHTS FOR DIGIFAB®

WEP Clinical (WEP) announced today that it has extended its partnership with BTG Specialty Pharmaceuticals (BTG), a division of Boston Scientific. Last year, WEP announced it would be partnering with BTG to supply the [...]

By Wep Clinical|2023-12-12T12:10:49+00:00March 1st, 2021|2021|
Read More

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logo WEP Clinical | Treatment Access Solutions | With Every Patient