medical writing

Acumen provides medical communications, medical writing and clinical development services to the biopharmaceutical industry, from strategy through regulatory submission. The company offers clinical and nonclinical medical writing, quality control and editorial services, narratives, document-level publishing, publications, project and submission management, medical consulting, and transparency and disclosure services.

clinical regulatory writingclinical trial disclosure and redactiondocument pre-publishinggraphic designmedical consultingmedical reviewproject managementpublicationsquality control and editorialsubmission managementtransparency and disclosure

AdMed creates industry-leading training for global leaders in the pharmaceutical and biotech sectors. Its in-house team includes doctorate-level medical directors and writers, project managers, designers, animators, and video producers. AdMed uses AI to simplify complex medical topics and offers solutions for training needs.

AI videoanimationaugmented realityinteractive videomicrolearning video productionpodcastsvideo productionvirtual classroomsworkshops

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.

biostatisticsclinical monitoringdata managementPharmacovigilance and safetyquality infrastructure and auditingSAS programmingsite feasibility, identification and selectionvalidation: CSV, GMP, GCP, GLP

AIM Biomedical Communications is a medical publications agency founded in 2012 by Agnella Izzo Matic, PhD, CMPP. It helps small-to-mid-sized pharmaceutical and medical device companies clearly explain their data to healthcare professionals, producing scientific and medical communications across the publication lifecycle.

copyeditingData Visualizationgraphic designjournal selectionliterature surveillance and gap analysismedical illustrationpublication planning

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)biostatisticsdata managementeCOAeConsentencryption at restevent-driven audit logRisk-Based Quality Management (RBQM)site monitoringtelevisitstrial logistics

AlphaLife Sciences provides AuroraPrime, an AI-powered pharmaceutical document authoring platform built for regulated life sciences. It supports end-to-end regulatory and medical authoring across the drug development lifecycle, including clinical, CMC, nonclinical, safety, labeling, and post-market documents. The company also offers AuroraPrime DocMind enterprise AI engine and AI-accelerated expert authoring services.

AI-powered regulatory authoringaudit trailsautomated QCcontent reuseeCTD document automationMicrosoft Word 365 add-inREST and Direct Data APIsVeeva Vault RIM integration

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 servicesbioanalysisbiostatisticsclinical monitoringclinical pharmacology trialsdata managementformulation developmentGLP and non-GLP preclinical evaluation studiesICH stability testingmanufacturingpreclinical safety testingProgram Management

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.

biostatisticsclinical operationsdata managementfeasibility assessmentIND preparation and submissionmonitoringpre-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.

biostatisticsclinical monitoringclinical trial designclinical trial managementdata managementpatient 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.

biostatisticsclinical trial designclinical trial executiondata managementpre-clinical and bench design and executionregulatory support

Columbia Data Analytics, LLC (CDA) is a consortium of economists, statisticians, epidemiologists, pharmacists, mathematicians, clinician scientists, and medical writers based in New York City (headquarters) and Ann Arbor, Michigan. CDA provides insights and interdisciplinary support using retrospective and prospective data, aiming to improve the efficiency of health care through rigorous research and interdisciplinary collaboration.

AI/machine learning algorithmsclinical trial data analysiseconomic modelingevidence synthesisexternal control arm studieshealthcare policy impact analysisliterature reviewmeta-analysismicrosimulationobservational study designoutcomes researchstatistical analysis

Confidence Pharmaceutical Research is a private, global full-service Contract Research Organization (CRO) providing tailored, end-to-end clinical trial management. It operates in the USA, Eastern and Western Europe, MENA, Latin America and APAC, with an active presence in 35+ countries and experience across diverse therapeutic areas.

clinical monitoringclinical trial managementdata management and biostatisticsfeasibility and site selectionmedical monitoringpharmacovigilancequality assuranceregulatory submissionssite contracting and paymentstranslations

Core Content Network connects writers and clients with immediate writing needs. Its dedicated team consists of experienced writing professionals, led by Dr. Sharon Rogers, PhD, ELS, who has 30 years of experience as a medical communicator in the pharmaceutical/biotechnology industries and 5 years as a freelance writer. The company provides regulatory writing and related medical writing and project management services.

document revieweditingformattingGrant Writingmeeting facilitationproject managementquality controlregulatory writingsummarizing scientific data

Cota Enterprises is a Kansas-based clinical research support company founded in 1995 by Rebecca Hoagland. It provides biostatistical analysis, clinical programming and data management, medical writing and regulatory support, CDISC specialization, and clinical design services to pharmaceutical, biotech, government, and research organizations, with a focus on data integrity, regulatory compliance, and scientific excellence.

Biostatistical analysisCDISC complianceClinical design servicesClinical programming (SAS)data managementregulatory support

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.

biostatisticsclinical research supportdata management

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.

biostatisticsclinical trial monitoringdata managementPharmacovigilance and safetyproject managementquality assuranceRegulatory Affairs

Dr. Vince Clinical Research is a full-service CRO built specifically for early phase drug development, specializing in Phase I-III clinical trials across a wide range of study designs, therapeutic areas and drug classes. Studies are conducted at its 80,000 square-foot research campus in Overland Park, Kansas, which houses a 100-bed Phase I clinical pharmacology unit, an in-house clinical laboratory and a cGMP-compliant pharmacy. The company was founded by Bradley D. Vince, DO, CEO and Chief Medical Officer.

biostatistics and programmingcGMP-compliant pharmacyclinical monitoringclinical trialsCTMSdata managementEDCeSourcein-house clinical laboratorymedical monitoringPhase I clinical pharmacology unitPK modeling and simulationPK/PD analysisproject management

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.

biostatisticsData Visualizationmedical translationsquality 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 trialsbiostatisticsclinical trial managementdatabase designdata managementmonitoringpharmacovigilanceproject managementRegulatory Affairs

Essential Data Corporation (EDC) is a nationwide provider of technical writing and documentation services, with 40 years of expertise and 500+ clients served. EDC's technical writers interview subject matter experts, streamline complex workflows, and deliver publication-ready documentation tailored to industries including healthcare, finance, technology, telecommunications, government, and manufacturing. Each project is overseen by a dedicated Engagement Manager at no additional cost.

documentationproposal writingregulatory writingscientific writingSOP writingtechnical writingtraining and eLearning content developmentwhite paper writing

ExecQuest is an executive search firm servicing the Pharmaceutical, Biotech, Medical Device and Diagnostics Industries. Lisa FitzGerald is Founder and President. ExecQuest sources, recruits, and places talent in full-time and contract positions, and also provides Medical Writing services to clients.

executive searchmedical communicationsrecruitingtalent placement