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 InsightsOleksandra Bystrova2025-04-21T10:53:03+01:00

WEP Insights

The WEP team is made up of industry leaders with expert knowledge and experience working in clinical trials, access programs, and market access strategies. Learn more from our Subject Matter Experts (SMEs) on important topics relevant to the successful design, delivery, and execution of projects across the clinical development pipeline. 

  • All Post
  • WEP Insights
Expanded Access in 2025: What the FDA’s New Q&A Guidance Document Means for Sponsors
11th November 2025/

Expanded Access in 2025: What the FDA’s New Q&A Guidance Document Means for Sponsors

Read More
Best Practices: Tips for Successful Site Initiation Visits
5th November 2025/

Best Practices: Tips for Successful Site Initiation Visits

Read More
Access Program Rescue:  Ensuring Continuity, Compliance, and Patient Care
8th October 2025/

Access Program Rescue: Ensuring Continuity, Compliance, and Patient Care

Read More
Partnering with a Strategic Expanded Access & Post-Trial Access Program Vendor
24th September 2025/

Partnering with a Strategic Expanded Access & Post-Trial Access Program Vendor

Read More
Real-World Data in Expanded Access Programs: How to Align with FDA Expectations
14th August 2025/

Real-World Data in Expanded Access Programs: How to Align with FDA Expectations

Read More
Named Patient Programs vs Compassionate Use Programs in the European Union
7th August 2025/

Named Patient Programs vs Compassionate Use Programs in the European Union

Read More
Balancing Cost and Quality: Why a Low-Cost Vendor Isn’t Always the Best Option
21st July 2025/

Balancing Cost and Quality: Why a Low-Cost Vendor Isn’t Always the Best Option

Read More
Why a Mobile Nursing Model with Full-Time, In-House Nurses is a Game-Changer for your Clinical Trials
13th June 2025/

Why a Mobile Nursing Model with Full-Time, In-House Nurses is a Game-Changer for your Clinical Trials

Read More
Redefining Clinical Trial Access: How Mobile Research Nursing is Solving Some of Industry’s Biggest Challenges
29th May 2025/

Redefining Clinical Trial Access: How Mobile Research Nursing is Solving Some of Industry’s Biggest Challenges

Read More
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logo WEP Clinical | Treatment Access Solutions | With Every Patient