At Specimens Inc., we provide specialized specimen collection and logistics tailored for clinical trials, research studies, and healthcare applications. With expertise in Good Clinical Practice (GCP) compliance, strict chain of custody handling, and nationwide mobile collection services, we ensure sample integrity and regulatory adherence for pharmaceutical companies, Contract Research Organizations (CROs), biotech firms, and healthcare providers.
Our services support decentralized clinical trials (DCTs), facilitating in-home and remote collections to enhance patient participation and improve retention rates. Whether collecting blood, urine, saliva, or tissue, our highly trained collectors ensure accurate, reproducible results that meet FDA, ICH, and industry regulatory standards.
🔹 Nationwide Coverage – Mobile specimen collection wherever and whenever it’s needed.
🔹 Regulatory Compliance – Strict adherence to GCP, FDA, HIPAA, and research protocols.
🔹 Sample Integrity – Secure handling and chain of custody for legally defensible research.
🔹 Industry Expertise – Trusted by CROs, biopharma, and research institutions for high-quality specimen services.
We offer nationwide specimen collection for decentralized and site-based clinical trials, ensuring sample accuracy and regulatory compliance.
✔ In-Home & Mobile Collections – Expanding access for participants who cannot visit traditional study sites.
✔ Site-Based Specimen Collection – Partnering with trial sites for standardized, protocol-driven specimen handling.
✔ Biofluid & Tissue Sample Collection – Blood draws, urine collection, buccal swabs, and more for clinical trials.
✔ Regulatory Compliance – Full adherence to FDA, ICH-GCP, HIPAA, and study-specific protocols.
Efficient handling of research specimens from collection to laboratory processing ensures accuracy and compliance.
✔ Centrifugation, Aliquoting, & Sample Preparation – Lab-ready processing following protocol-specific requirements.
✔ Sample Storage & Transport – Cold chain management, time-sensitive handling, and compliance with IATA shipping regulations.
✔ Study-Specific Documentation – Customized labeling, Chain of Custody (CoC) tracking, and compliance reporting.
✔ Collaboration with CROs & Biopharma – Supporting clinical trials, bioanalysis, and drug development research.
Strict adherence to clinical and regulatory standards ensures that specimens are handled accurately, securely, and legally.
✔ GCP-Compliant Handling – Adhering to ICH-GCP and FDA guidelines for clinical research specimens.
✔ Legally Defensible Chain of Custody – Secure documentation ensuring sample authenticity and trial integrity.
✔ HIPAA & GDPR Compliance – Protecting patient data through secure collection, transmission, and reporting.
We bridge accessibility gaps in clinical research by bringing specimen collection directly to study participants.
✔ Mobile & In-Home Specimen Collection – Expanding patient access beyond traditional sites.
✔ Enhanced Retention & Compliance – Reducing participant burden, improving adherence, and maintaining study engagement.
✔ Remote & Hybrid Clinical Trial Support – Supporting hybrid trial models with site-based and remote collections.
✅ Pharmaceutical Companies & Biotech Firms – Supporting drug development, diagnostics, and therapeutic research.
✅ Contract Research Organizations (CROs) – Providing end-to-end collection, processing, and logistics for research studies.
✅ Academic & Medical Research Institutions – Assisting with specimen-based clinical studies and epidemiological research.
✅ Healthcare & Diagnostic Companies – Offering specimen collection for biomarker discovery, disease screening, and molecular research.
Specimens Inc.
235 Peachtree Street NE, Suite 400, Atlanta GA 30303
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