Clinical Research Phlebotomy: Mobile Specimen Collection for Decentralized Clinical Trials

Enable decentralized and hybrid clinical trials with our nationwide network of protocol-trained phlebotomists. Collect research specimens directly from study participants in their homes, improving retention and expanding geographic reach while maintaining rigorous compliance.

IRB Compliant
Protocol Trained
All 50 States
Real-Time Documentation

Supporting the Future of Clinical Research Through Mobile Specimen Collection

Decentralized clinical trials (DCTs) are transforming pharmaceutical research by bringing studies directly to participants rather than requiring them to travel to distant research sites. MobilePhlebotomy.app provides the critical specimen collection infrastructure that makes DCTs and hybrid trials possible at scale—connecting research organizations with verified, protocol-trained phlebotomists across all 50 states.

Our mobile research specimen collection services support Phase I through Phase IV studies, observational research, biomarker studies, and pharmacokinetic sampling. By enabling in-home specimen collection, we help sponsors and CROs reduce participant burden, improve retention rates, expand into underserved geographic areas, and accelerate enrollment timelines.

Every phlebotomist in our research network receives protocol-specific training before assignment to your study. We understand the critical importance of adherence to collection timing, specimen handling requirements, chain-of-custody documentation, and adverse event reporting. Our quality systems are designed to meet the rigorous standards expected by sponsors, CROs, and institutional review boards.

Clinical Research Specimen Collection Services

Decentralized Trial Support

In-home specimen collection for fully decentralized and hybrid clinical trials. Reduce site visits, improve participant experience, and expand geographic reach.

Protocol-Specific Training

Phlebotomists receive comprehensive training on your study protocol including collection sequences, timing windows, specimen handling, and documentation requirements.

Flexible Participant Scheduling

Convenient scheduling options that accommodate protocol-required visit windows, fasting requirements, and participant preferences to maximize retention.

Real-Time Documentation

Comprehensive collection records with timestamps, specimen condition notes, deviation reports, and chain-of-custody documentation for audit readiness.

Multi-Site Coordination

Nationwide coverage for multi-site studies. Consistent collection quality across all locations with centralized coordination and quality monitoring.

PK & Timed Collections

Support for pharmacokinetic studies and other time-sensitive collection protocols. Multiple draws within required windows with precise timing documentation.

How Research Specimen Collection Works

1

Protocol Review

Review protocol & setup

2

Training

Phlebotomist selection & training

3

Scheduling

Participant scheduling

4

Collection

In-home specimen collection

5

Processing

Specimen processing & shipping

6

Reporting

Documentation & quality reporting

Research Organizations We Support

Pharmaceutical Sponsors
Contract Research Organizations
Academic Medical Centers
Biotech Companies
Central Laboratories
Site Networks
Patient Advocacy Groups
Government Agencies

Frequently Asked Questions

Request a Customized Proposal

Tell us about your research study's specimen collection needs and we'll create a customized proposal.

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Need help? Contact us:

support@mobilephlebotomy.app

Enable Decentralized Clinical Trials with Mobile Specimen Collection

Partner with the Nation's Leading Research Specimen Collection Network