biostatistics

mission is to advance healthcare & life sciences through collaboration and innovation. Founded in 2015, Adeco LLC is a Black-owned Small Business located in Houston, Texas — the World’s Largest Medical Center, Energy Capitol of the World, and Space City. We provide analytical, clinical, managerial, and technical solutions for the optimum performance of healthcare and other organizations. We were a Centers for Disease Control and Prevention (CDC) COVID-19 Vaccination Program Provider Site; now an ARPA-H CX Hub Member with CDC One Lab VR Coordination, and ongoing Pharmaceuticals & Therapeutics Research. We previously partnered with NVIDIA, “the engine of modern artificial Intelligence (AI) and generative AI.” This collaboration, which positioned us at the forefront of generative AI, concluded on August 13, 2026. We are a United Nations Vendor. We are a Google Cloud Partner. We are a Razer.

3D printing4D printingclinical data managementcloud computing servicesEpidemiologyPharmacometricsVR/ARweb design

Advanced Clinical is a global research services and strategic resourcing organization providing Contract Research Organization (CRO), Functional Service Provider (FSP), and Strategic Resourcing solutions across North America, Europe, LATAM, and APAC. Established in 1994, it partners with pharmaceutical, biotechnology, and medical device clients to deliver a better clinical experience across the drug development journey.

clinical monitoringdata managementmedical writingpharmacovigilance and safetyquality infrastructure and auditingSAS programmingsite feasibility, identification and selectionvalidation: CSV, GMP, GCP, GLP

Alethium is a full-service CRO that runs every service on its own digital-first Clinical Data Platform (CDP). Since 2008 it has supported more than 250,000 participants in complex U.S. and international decentralized and hybrid trials for emerging and mid-sized biopharma companies and CROs.

Advanced analyticsautomation engineBehavior-Driven Development (BDD)data managementeCOAeConsentencryption at restevent-driven audit logmedical writingRisk-Based Quality Management (RBQM)site monitoringtelevisitstrial logistics

Altasciences is a mid-size early phase contract research organization (CRO/CDMO) in Canada and the U.S., offering biopharmaceutical companies a flexible approach to early drug development, including preclinical safety testing, clinical pharmacology (Phase I to Phase II), bioanalysis (preclinical to Phase IV), research services, and manufacturing and analytical services. Founded as a CRO in 1995, it became Altasciences in 2013.

analytical servicesbioanalysisclinical monitoringclinical pharmacology trialsdata managementformulation developmentGLP and non-GLP preclinical evaluation studiesICH stability testingmanufacturingmedical writingpreclinical safety testingprogram management

AltraBio is a contract research company specializing in advanced biological data analysis and bioinformatics services, helping biopharma, cosmetic, and clinical R&D organizations extract insights from cytometry, omics, and medical data using AI, machine learning, and biostatistics. It serves pharmaceutical companies, biotech startups, dermo-cosmetic leaders, and university hospitals worldwide.

automated gatingbioinformatics pipeline developmentbiomarker discoverybulk transcriptomicscytometry data analysishigh-dimensional panel analysismachine learningpatient stratificationproteomicsreal-world data miningsingle-cell RNA-seq analysisstatistical modelingtarget identification

ASG provides decision insight for leaders in the national security and commercial spaces. The company offers advanced data analytics and visualization, operations research, decision science, resource allocation expertise, budget and financial analytics, and intelligence analysis to government clients, and biostatistics and industrial process optimization to commercial clients. Its analysts support strategic planning and operational mission execution.

budget and financial analyticsData AnalyticsDecision scienceindustrial process optimizationintelligence analysisoperations researchresource allocationVisualization

Annovis Bio is a Phase 3 clinical-stage biotechnology company developing transformative therapies for neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. Its goal is to develop effective treatments by restoring nerve cell function and improving cognitive and motor abilities in patients. The company was founded in 2008 by Dr. Maria Maccecchini and is listed on the NYSE under ANVS.

clinical developmentclinical trial operationsdrug discoveryGMP operationspilot plant productionprocess chemistry R&Dregulatory strategy and FDA submissions

Arroyo Research, Inc. (ARI) provides quality customized Phase I-Phase-IV clinical trial services, connecting sponsors with experienced, prescreened investigators and sites, and offering site feasibility and patient recruitment tools.

clinical monitoringclinical operationsconsultingdata managementInvestigator Selectionmedical devicesproject managementquality assuranceRegulatory AffairsTechnology

Axella Research is a full-service clinical research organization for emerging biopharma, device and diagnostic companies. It combines FDA regulatory strategy, biostatistics, a community-based physician network and technology-integrated trial operations, with deep experience in oncology and urology. The company offers fee-for-service or shared-risk partnerships, and its operations run on Ecosera, an open clinical research platform.

clinical operationsdata managementfeasibility assessmentIND preparation and submissionmedical writingmonitoringpre-IND meetingsproject managementregulatory strategysite start-upSMO servicesstatistical programming

Beaufort is a MedTech-specialized contract research organization (CRO) that transforms MedTech possibilities into realities through precise, agile solutions that accelerate innovations to market. With 20+ years of MedTech experience, 1000+ global clinical trials, and 500+ global regulatory submissions, Beaufort provides clinical trial and regulatory support for medical devices, IVD, and digital health.

clinical monitoringclinical trial designclinical trial managementdata managementmedical writingpatient recruitmentquality assuranceregulatory strategyregulatory submissionssafety managementsite management

Boulder Clinical Science is a CRO specializing in clinical trial protocol design and execution across all phases (1-4) of the drug/device development cycle. It combines academic and industry expertise with PhD-trained Clinical Scientists and Biostatisticians with a minimum of 20 years of clinical trial industry experience, plus seasoned Clinical Trial Managers and Monitors.

clinical trial designclinical trial executiondata managementmedical writingpre-clinical and bench design and executionregulatory support

ClineEpi Partners is a physician-led global consulting firm specializing in epidemiology, biostatistics, real-world evidence (RWE), health economics, clinical trial strategy, and global health security. Its team includes U.S. and European-based experts with experience leading NIH-, FDA-, CDC-, and DOD-funded studies, serving pharmaceutical, biotechnology, and public health sectors with a presence in North America and Europe and partnerships in Africa and Latin America.

clinical trial strategyEpidemiologyglobal health securityhealth economicsHEOR supportimplementation science consultingmanuscript writingreal-world evidence (RWE)scientific communicationsstakeholder engagement

Data Solutions, LLC provides biometric services and clinical research support to pharmaceutical and biotechnology industries. Established in 1997, the company offers biostatistics services for phase I-IV clinical trials, data management, and medical writing. Most statisticians hold a PhD in statistics or biostatistics.

clinical research supportdata managementmedical writing

DCN Dx is an immunoassay CDMO and IVD CRO based in Carlsbad, CA. It provides contract development and manufacturing services, including lateral flow assay development, consumable and cassette design, custom readers, contract manufacturing, aseptic filling, and reagent lyophilization, along with clinical research services such as trial management, site development, biostatistics, data management, and regulatory consulting. Its 35,000+ sq. ft. facility is ISO 13485- and ISO 9001-compliant.

aseptic fillingbiospecimen collectionsclinical trial managementconsumable and cassette designcontract manufacturingcustom reader designdata managementELISA developmentlateral flow assay developmentreagent lyophilizationRegulatory consulting

Homeadmin2025-05-07T17:04:32+00:00 DP Clinical Has Been Providing CRO Services for Over 30 Years!Whether you need a full complement of clinical trial services or only specific service offerings, we will provide the expertise, flexibility, and innovation to meet your study needs. Loading... We are proud to celebrate a major milestone for our client, Spectral AI, following the FDA’s De Novo clearance of its Deep View® System, an innovative AI-powered imaging technology designed to support burn wound assessment and treatment decisions. Learn More We're proud to share that our Director of SCI Programs, Jim Hamer, and Medical Advisor, Dr. Lisa Ruppert, were honored with the FASIA Award at the American Spinal Injury Association (ASIA) Annual Meeting 2026! Learn More Flexible CRO providing full and functional services since 1994. CRO specializing in Critical Care, Dermatology, Infectious.

clinical trial monitoringdata managementmedical writingpharmacovigilance and safetyproject managementquality assuranceRegulatory Affairs

Eminence Clinical Research, Inc. is a full-service clinical trial and research consulting firm that provides clinical data management-EDC and regulatory-quality-compliance consulting services and products. It partners with corporations, physicians, and clinical trial sites to advance medical research and bring new products to market, with expertise grounded in 40+ years of experience in the medical device and hospital-based research industries.

clinical affairs trainingclinical trial design and managementdata managementEDC system design and buildmedical writing and scientific publicationsquality assuranceregulatory submissions

Empive is a service provider offering Information Technology solutions and Healthcare Services across commercial, Non-Profit, and Government sectors. Offerings range from innovative Healthcare solutions to Database Management and Infrastructure support. It is a service-disabled veteran and minority woman-owned small business. Its team includes board-certified, licensed, and experienced professionals with expertise in healthcare, clinical research, data management, database technology, computer networking, systems evaluation, integration, testing, and met

business analysisclinical researchClinical trials site management and monitoringdata analysisdatabase administrationdatabase managementIndividual and group therapyMental health counsellingProject/Program Managementsoftware supportStaff augmentation

Emtex is an independent company founded in 2001 that offers professional medical writing and related services worldwide to the pharmaceutical (human & veterinary), biotech, medical device and other industries, CROs and academic institutions. With over 25 years of experience and involvement in over 1200 projects, it provides regulatory medical writing, research & insights, media & communications, and training services.

data visualizationmedical translationsmedical writingquality controlregulatory medical writingstatistical analysistraining

eRIC SOLUTIONS is a full-service CRO and regulatory affairs partner founded in 2016 and headquartered in Plantation, Florida, with operations in India and partners in Argentina, Hungary, Romania, and Australia. It runs ICH-GCP Phase I–IV clinical trials and the data, biostatistics, safety, and regulatory work behind them for pharma, biotech, and medical-device sponsors in the US, Europe, and Asia.

AI agents for clinical trialsclinical trial managementdatabase designdata managementmedical writingmonitoringPharmacovigilanceproject managementRegulatory Affairs

Frontage Laboratories, Inc. is a global pharmaceutical development organization (PDO) and CRO providing integrated, science-driven product development services throughout the drug discovery and development process. It assists clients in advancing molecules through development to commercial launch, enabling innovators, generic, and consumer health companies to file IND, NDA, ANDA, BLA, and 505(b)(2) submissions in global markets.

analytical servicesbioanalysiscentral lab servicesclinical trial material manufacturingcommercial manufacturingDART servicesdata managementDMPKdrug developmentdrug discoveryformulation developmentgenetic toxicologyGMP routine testingmass spectrometrymethod development and validationsafety pharmacologystability programsstatistical programmingtoxicology

InClin is a full-service Contract Research Organization (CRO) with offices in San Mateo, California, and Sydney, Australia. It partners with biotech and pharmaceutical companies to conduct Phase 1 through Phase 4 clinical trials for developing novel therapies, offering clinical research services as an integrated single-source solution or as standalone services.

clinical data managementclinical monitoringclinical operationsclinical trial managementdrug safetyeTMF managementfeasibility assessmentmedical monitoringmedical writingproject managementquality assurancestatistical programmingstrategic consulting

K3 Innovations is an AI-native, full-service clinical research organization (CRO) providing biostatistics, clinical data management, clinical operations, safety and evidence, and preclinical data science services. Its senior teams run studies end to end, supported by SPARC, its own AI trial automation platform that compresses biometrics timelines from months to days.

AI-driven clinical trial automationclinical data managementEDC buildFSP resourcingmedical writingPharmacovigilancereal-world evidencerisk-based monitoringsite monitoringstatistical programming

genomics pioneer and the preeminent commercial strategist for biotech startups, Patricia has remained at the forefront of bioinformatics for over 40 years Developing the commercial strategy for the Human Genome Project with Dr. J. Craig Venter at NIH early in her career, our CEO & Founder Ms. Patricia Ward was heavily engaged in the infancy of the bioinformatics field and participated in early research with many noted bioinformaticians. Kingston Ward was formed by seasoned senior managers with more than 35 years of experience, including several years in senior positions at Big 4 consultancies. Our team’s professional track record, and integrated network of highly qualified specialists with hands-on expertise in the design and delivery of analytic platforms, allows us to provide custom algorithms that meet the requirements of any project. Kingston Ward Advisory Group, Inc. is a.

AI and processing servicesBioinformaticsbusiness process outsourcingbusiness process re-engineeringCloud migrationdata analytics and visualizationFinancial accounting and reportingloan underwritingManagement consultingnatural language processingSaaS implementationSemantic web technologiesTechnology Modernization