Pharmacovigilance

Abiozen is a U.S.-based life sciences platform and B2B supplier of specialty chemicals, building blocks, intermediates, reference standards, and generic and GMP APIs for licensed pharmaceutical manufacturers, biotech, and research institutions worldwide. Founded in 2024, it operates as a technology-driven intermediary connecting suppliers, laboratories, and research teams, with orders routed through its Buffalo Grove, Illinois facility.

biostatistics and SAS programmingcustom synthesisDMF filing supportFDA submission preparationGMP compliance consultingprocess development and scale-upQC testing (HPLC, GC-MS, FT-IR, dissolution)supply chain and distribution

Company / About Us / History History Putting the Spotlight on Biotech Innovation How Can We Help? SCROLL Company Origins In the spring of 2022, Allucent came into being with the merger of several high-performance companies serving the specialized needs of small and mid-size biopharma. Derived from the Latin verb alluceo, Allucent means to shine a light upon something or to create an opportunity. With a new name and bold branding, Allucent united the company and its employees under one purpose: putting the spotlight on biotech innovators and helping them deliver treatments to patients with unmet needs. OUR CORPORATE TIMELINE Partner With the A-Team Let us know how we can help you bring new therapies to light. Get in touch to get started. Schedule a Consultation Join the A-Team Want to help small and mid-size biopharma companies change the therapeutic landscape? View Open Jobs Subscribe.

AI-enabled clinical development (LucentAI)biostatistics and statistical programmingclinical development operationsclinical pharmacologydata managementGxP consultingmedical monitoringmodeling and simulationpatient recruitment and retentionregulatory strategyregulatory submissionsstudy start-up and site feasibility

Ennov provides an AI-powered Unified Compliance Platform for Life Sciences, supporting the entire product life cycle across Regulatory, Quality, Clinical, Pharmacovigilance, and Commercial domains. Its solutions eliminate silos and reduce complexity across regulated processes, and are used by more than 650 Life Sciences companies worldwide. Ennov also offers expert services including hosting, implementation, migration, training, support, and customer success.

AI-powered unified compliance platformclinical data managementcloud or on-premises deploymentcustomer supportimplementationmigrationprivate cloud hostingQuality Managementregulatory information managementtraining

CCS Associates (CCSA) is a small business providing leading-edge scientific services in product discovery and development to government agencies and the pharmaceutical and biotech industries. It is a full-service CRO offering services from discovery to approval, with more than 40 years of client success. CCSA was founded by Caroline C. Sigman, PhD, and its projects have led to 5300+ IND, NDA, CTA, DMF, IDE, and INAD submissions.

Bioinformaticsclinical trial monitoringeCTD publishingpharmacologyRegulatory Affairsscientific and medical writingstrategic-planningtoxicology

Cloudbyz provides a unified AI-enabled eClinical trial management platform natively built on the Salesforce platform. Its products cover clinical trial management (CTMS), clinical trial financial management (CTFM), electronic trial master file (eTMF), electronic data capture (EDC), safety and pharmacovigilance, randomization and trial supply management (RTSM), patient recruitment, eConsent, and project portfolio management, along with AI agents for life sciences workflows.

AI agentsBusiness consultingclinical trial managementelectronic data capturepatient recruitmentprofessional servicesregulatory submissionsREST API integrationsSalesforce platform development

CRS is a Women-Owned Small Business founded and run by physicians with decades of clinical research experience. It provides clinical research support services to government, companies, and other organizations, with a focus on efficiency, quality, and customer satisfaction. Its leadership team includes physicians with extensive NIH clinical research experience.

Audit preparationclinical data managementclinical informaticsclinical monitoringdata extractiondata verificationEDC developmentRegulatory Compliancesite coordination

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 monitoringmedical writingquality assuranceregulatory submissionssite contracting and paymentstranslations

Cycle Pharmaceuticals is a pharmaceutical company established in 2012 that provides treatments and support services for patients with rare and life-changing conditions in oncology, neurology, metabolics, and immunology. It focuses on improving medication forms and offering individualised patient support, including a Free Goods Programme for patients unable to pay for rare disease medication.

improving medication forms (smaller tablets, temperature stable, dissolvable tablets)patient support servicesproduct launchRegulatory Affairs

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 managementmedical writingmonitoringproject managementRegulatory Affairs

Global Bridge Pharmaceutical Pharmaceutical Supply Chain Resilience Partner ​ Global Bridge Pharmaceutical is a pharmacist-led pharmaceutical distribution and consulting company committed to improving access to safe, affordable, and high-quality medicines. Headquartered in Charlotte, North Carolina, our core operations focus on supporting healthcare providers, pharmacies, hospitals, specialty practices, and public health organizations across the United States through compliant sourcing, supply chain support, and strategic pharmaceutical services. Learn More OUR IMPACT LEARN MORE Learn More OUR MISSION And vision Support healthcare providers with pharmaceutical sourcing solutions.Combine pharmacist expertise with strategic industry partnership Assist with procurement, access, and medication support services.Focus on compliance, responsiveness, and continuity of care Why Global Bridge.

consulting servicesdrug donation programsdrug safetymanaged access programsnamed patient supply coordinationpharmaceutical distributionpharmaceutical exportpharmaceutical procurementsupply-chain support

Guosa Life Sciences is an integrated clinical development enterprise and the Network Coordinating Center of the Clinical Development Network. It helps sponsors, biotechnology companies, governments, academic institutions and global health organizations accelerate development of innovative medicines through four integrated platforms: GLS Institute, GLS Academy, the Clinical Development Network and Solutions. It operates across the US, Sub-Saharan Africa, Asia, Europe and MENA, with 35+ countries of reach and 60+ research-ready sites.

biomarker analysisbiospecimen managementCapacity developmentclinical developmentcold chain logisticsGCP audits and inspection readinessIMP distributionregulatory strategy and submissionsstatistical analysis

L'Institut Pasteur du Maroc (IPM) est un établissement pharmaceutique industriel public, placé sous la tutelle du Ministère de la santé. Il a pour missions la fabrication, l'importation et la commercialisation des sérums, vaccins et produits biologiques, ainsi que la recherche scientifique, la santé publique et la formation.

Analyses de biologie médicaleContrôle de la qualité des vaccins et produits biotechnologiquesformationProduction de milieux de culture et réactifs de laboratoireProduction de vaccins, sérums et produits biotechnologiquesRecherchevaccination

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 automationbiostatisticsclinical data managementEDC buildFSP resourcingmedical writingreal-world evidencerisk-based monitoringsite monitoringstatistical programming