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description=Global contract research organization delivering CRO services, regulatory support, and clinical development solutions for biopharma.;

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contract research organization for biopharma allucent solutions solutions small and mid sized biotech companies have distinct development challenges from therapeutic innovations through the clinical process to approval solutions overview schedule a consultation therapeutic expertise clinical development study start up site feasibility ignite site network patient recruitment retention data management biostatistics statistical programming medical monitoring clinical pharmacology drug development strategy regulatory modeling simulation end to end pharmacokinetics embedded pharmacologist regulatory strategy cmc preclinical clinical strategy biostatistical consulting regulatory submissions gxp consulting drug safety pharmacovigilance clinical trial safety post marketing pharmacovigilance government public health services blogs empowering small biotechs conquering clinical trial challenges with data management champions podcasts podcast artificial intelligence gcp compliance inspection readiness in clinical trials therapeutic expertise therapeutic expertise as a small or mid sized biotech company your organization expands the boundaries of scientific innovation to treat the most complex and challenging diseases therapeutic expertise overview schedule a consultation solutions therapeutic areas oncology hematology infectious disease vaccine neuroscience immunology inflammation cardiometabolic disease cross over therapeutics cell gene therapy rare diseases pediatrics industry featured articles harnessing antibody drug conjugates adcs in oncology pathways to clinical success blogs common disease mechanisms in neurodegenerative disorders insights for the development of disease modifying therapies company company today allucent delivers innovative strategies and robust solutions based on over 30 years of background in regulatory trends therapeutic experience and operational expertise company overview schedule a consultation about us history news events leadership team mission vision and values press release allucent names paula brown stafford as ceo industry veteran to lead next phase of global cro s expansion press release allucent recognized with two cro leadership awards resources resources explore educational resources from allucent cro including webinars and expert insights designed to help small and mid size biotech companies address clinical research and development challenges all topics types schedule a consultation blogs case studies podcasts webinars white papers expert conversations brochures guides industry featured articles posters infographics blogs cell therapy manufacturing analytical testing validation and regulatory considerations blogs understanding the integrated summary of immunogenicity careers careers our mission is to help bring new therapies to light when you work at allucent that means rolling up your sleeves and applying your unique skill set expertise and knowledge to build partnerships with our clients in their pursuit to develop new life improving treatments careers overview contact us job listings internship and fellows programs watch our corporate video contact us contact us the full service cro partner for biopharma clinical development schedule a consultation accelerate your clinical trials with expert oncology cro services read more maximize your clinical research potential with the leading neuroscience cro learn more ceo paula brown stafford interview with onyx read more full service cro solutions accelerating biopharma innovation from early stage to post approval at allucent we are a global full service cro partnering with small and mid size biopharma to advance therapies through every phase of drug development and clinical trials from early stage to post approval combining deep therapeutic expertise with a nimble collaborative approach we specialize in oncology neuroscience and infectious diseases with cross therapeutic experience in rare diseases and advanced therapies through flexible regulatory solutions and scientific insight we help biopharma accelerate development overcome complexity and deliver innovative treatments to patients worldwide your purpose is our purpose at allucent we are as vested in your goals and success as you are we re not just a service provider but a dedicated partner helping you solve your toughest challenges with a personal and flexible style tailored for you request a proposal therapeutic expertise allucent focuses on supporting breakthrough science from small and mid sized biotechs because you address the most complex and challenging disease states learn more how can we support your drug development journey a team expertise discovery discovery early phase early phase late phase late phase post marketing approval post marketing approval at allucent our a team experts are spotlight focused on your needs and uniquely adept at foreseeing and overcoming the challenges that routinely appear in complex therapeutic areas indications and modalities we help guide your science through the complexities of drug development to bring needed therapies to light for patients around the world click through the path above to see how our experts support your distinct needs with deep experience in critical areas that are often hard to source for smaller companies therapeutic expertise in complex categories where specialized support is essential the operational prowess needed to help you move forward efficiently and effectively an integrated cross discipline expert approach customized to your needs partnership and collaboration at the center of all we do allucent provides comprehensive support in the identification and validation of your potential drug candidates enabling you to make informed decisions and advance promising compounds to the next stages of development regulatory strategy and product development we help you navigate the complex regulatory landscape and ensure successful development and approval of drugs expertise includes regulatory intelligence therapeutic knowledge global strategy ind and nda submissions orphan drug designation and pediatric investigation plans clinical pharmacology our deep experience delivers drug development insights through designing and conducting studies to assess pk pd first in human studies poppk simulation and modeling and clinical trial simulation learn more at allucent we deliver expert knowledge the right global network across more than sixty countries and innovative data driven solutions to set a strong foundation for complex early studies and for your subsequent trials we deliver a comprehensive set of services to help drive your drug development program strong preclinical capabilities including in vitro and in vivo studies clinical trial design including first in human dose escalation and proof of concept data management and analysis allucent delivers accurate and timely data to support decision making and regulatory submissions biostatistical programming full time statistical consultants provide in depth support for complex needs and become part of your core team to ensure proper study design and planning collaboration and communication regular updates transparency and a collaborative approach help ensure great working relationships and success learn more across phase ii iii trials and through regulatory submissions our global experts work as your partners applying our insights and customized services to help ensure the highest quality research and improve outcomes we work with you to gather comprehensive data on the safety and efficacy of your investigational drugs large scale clinical trial expertise we have a strong track record of managing large scale phase iii clinical trials global footprint with hundreds of years of experience across allucent we have the expertise to conduct multi center and multinational trials to ensure diverse patient populations are represented study start up efficient study start up is crucial to meet project timelines we pride ourselves on timeliness and speed site selection and feasibility risk mitigation adaptability and integration of systems and technology patient recruitment and retention allucent understands the patient journey and how to ensure enrollment targets are met in a timely manner learn more once approved allucent consulting applies our post marketing study expertise to help you demonstrate the real world value of your products and collect insights to help make the regulatory case for patients around the world post marketing surveillance and pharmacovigilance we design and implement post marketing surveillance programs including post approval safety studies pass to monitor the long term safety and effectiveness of the drug learn more study experience 1 100 clinical trials conducted 70 countries worldwide 825 regulatory submissions per year 105 approved and marketed products clinical pharmacology experience 650 drugs supported all modalities routes of administration and therapeutic areas 6 650 pk pd tk qtc translational analyses 400 poppk and e r modeling dose and trial simulations regulatory submissions and experience 12 former regulators 6 regulatory agencies 825 annual regulatory submissions 105 successful marketing applications welcome to a whole new journey where breakthrough innovation from small and mid size biopharmas has a go to partner to light the way through complexities of clinical development we are allucent our focus is on you therapeutic expertise the allucent centers of expertise aces are designed structured and resourced to deliver comprehensive trial and regulatory strategy effective patient focused recruitment plans and solutions that meet your specific needs oncology hematology immunology inflammation neuroscience cell gene therapy cardiometabolic disease rare disease infectious disease featured content industry featured articles digital technologies transforming neurodegenerative trials learn more webinar proactive cohort management for mastering dose escalation in early phase oncology development watch now whitepaper advancing neurodegenerative disease trials with digital health technologies a regulatory aligned approach learn more view all resources 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 request a proposal or speak with one of our experts contact us solutions clinical development clinical pharmacology regulatory strategy drug safety pharmacovigilance government public health services therapeutic expertise oncology hematology infectious disease vaccine neuroscience immunology inflammation cardiometabolic disease company about us news events industry recognition north american headquarters 2000 centregreen way suite 300 cary north carolina 27513 united kingdom headquarters 1st floor one station square bracknell berkshire rg12 1qb united kingdom european headquarters stationsplein noord oost 438 1117 cl schiphol the netherlands allucent all rights reserved privacy policy modern slavery english francais