Leden van de ACRON

Op dit moment zijn 45 bedrijven lid van de ACRON. Hiermee vertegenwoordigen wij ongeveer 1200 medewerkers in de CRO branche in Nederland.

Het doel van de ACRON is om zoveel mogelijk CRO’s in Nederland te vertegenwoordigen, van ZZP’er tot mutlinational. Wilt u zich ook bij ons aansluiten? Het secretariaat stuurt u graag en vrijblijvend een informatiepakket. Bekijk hieronder het actuele ledenoverzicht van de ACRON.

Ledenoverzicht ACRON

  • ABL

    ABL is an independent contract bioanalytical laboratory since 1969, located in Assen. ABL is specialized in the analysis of endogenous and exogenous compouns in biological matrices derived from humans and animals.

    Mw. M.J. Dröge melloney.droge@ardena.com
    Dhr. A. Muntendam alex.muntendam@ardena.com
    Website: http://www.ardena.com

  • Alimentiv BV
    Alimentiv BV

    Alimentiv is headquartered in London (Canada) with offices in San Diego (California, USA) and Amsterdam, (The Netherlands) providing global coverage for our services. Our capabilities include a comprehensive range of clinical research services, from program evaluation and design to trial implementation, site monitoring, datamanagement and the analysis, interpretation and reporting of results.

    A recognized leader in clinical trial research, Alimentiv is well connected to science and discovery with our global network of IBD specialists and key opinion leaders.

    Dhr. H. Hoogeveen hans.hoogeveen@alimentiv.com
    Website: https://www.alimentiv.com/

  • AUTHOR! Et al B.V.
    AUTHOR! Et al B.V.

    Founded in 1998, AUTHOR! has gained extensive experience in providing expert medical writing services and data analysis support for a large number of pharmaceutical and biotechnical companies throughout Europe and the USA.

    Mw. A. te Velde atevelde@author.nl
    Mw. A. van Hest avhest@author.nl
    Dhr. P. van Ewijk pvewijk@author.nl
    Website: http://www.author.nl

  • BiKE

    The UMCG has over 50 years of biobanking research experience, both clinical as well as population studies. The oldest (Vlagtwedde-Vlaardingen, 1965) and largest population-based studies (LifeLines) originate from the UMCG, and all leading clinical research groups have organized clinical biobanks, like COPD, renal failure, transplantation, several cancers, gastro-intestinal diseases, etc. UMCG biobanking researchers are involved, often in a leading position, in all major European biobanking initiatives, as well as in the national biobanking structures (BBMRI-NL, PSI).

    Knowledge on the logistics of biobanking research is not found in textbooks, neither on dedicated statistical analyses or laboratory procedures for large scale data and samples. Because of the long-lasting experience, scientists and policy makers with plans or problems on biobanking increasingly contact UMCG/LifeLines. These questions come from local colleagues and (inter)national researchers.

    To embed this knowledge and expertise in the UMCG and LifeLines, BiKE has been established: the Biobanking and cohort studies Knowledge and Expertise Center. BiKE provides a range of services for biobank researchers: notably teaching, large scale data handling & storage, bio sample handling & long term storage, Biobanking ICT infrastructures.

    Dhr. B. Scheerder b.scheerder@umcg.nl
    Dhr. J. Sikkema j.sikkema@umcg.nl
    Dhr. J.M. Wijbenga j.m.wijbenga@umcg.nl
    Website: www.biobank.bike


  • Casahombre

    Casahombre is the Life Science Consultancy company that can make a difference for everyone trying to Create Value from Science. Casahombre is owned by Arnoud Huisman, a highly skilled Senior Executive in the Life Sciences industry with more than 25 years of success spanning pharmaceuticals, biotech, diagnostics and food & nutrition. His broad areas of expertise include innovation, leadership in performance, focus and strategy, M&A, P&L, marketing and product development.

    Throughout his executive career, Arnoud has held several leadership positions, amongst others at Biotrial, NIZO, PRA Health Sciences, and Pharma Industry (Wyeth and Solvay). During his time at PRA, he served as Vice President of Clinic, Senior Vice President of Global Business Development and Senior Vice President of Alliance Management, where he succeeded in winning projects worth approximately $750 million and establishing preferred provider contracts with both Large Pharma as Biotech.

    Arnoud holds an MSc in Human Movement Sciences from the Free University, Amsterdam. As a seasoned board member, he has held board positions with ACRON, EUCROF, Dutch Clinical Trial Foundation and Delphi BioScience. He speaks both English and Dutch fluently.

    Dhr. A. Huisman arnoud@casahombre.nl
    Website: http://casahombre.nl

  • Castor EDC
    Castor EDC

    Founded in 2012 by healthcare and research professionals who experienced problems with data management and a lack of user-friendly tools, Castor EDC is an easy-to-use cloud solution for securely capturing clinical research data and running clinical trials. We have a suite of solutions that can support CRO’s by delivering a modern, well designed, user friendly and capable EDC system with top rated customer support and services.Our goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which we maximize the impact of data through reuse.

    Dhr. F. Morang floris.morang@castoredc.com

  • Centre for Human Drug Research
    Centre for Human Drug Research

    Centre for Human Drug Research (CHDR) provides a full range of early stage clinical pharmacology services. CHDR specializes in early proof of pharmacology and in the complex process of drug development, we offer an efficient route towards proof of concept in patients. By conducting highly informative early-phase clinical studies, development risks can be minimized and costs can be reduced.

    Dhr. Prof. J. Burggraaf KB@chdr.nl
    Dhr. Dr. P. Peeters PPeeters@chdr.nl
    Dhr. Dr. R. Zuiker RZuiker@chdr.nl
    Website: http://www.chdr.nl

  • Clinfidence B.V.
    Clinfidence B.V.

    Clinfidence provides high quality clinical data management and pharmacovigilance services for clinical trials since 2016. Our highly experienced and dedicated people take a client-oriented approach to provide clients with the best solutions that fit their clinical trial.

    Mw. Nicole Spelier-Claessens nicole.spelier@clinfidence.com
    Website: https://www.clinfidence.com/

  • Clinical Trial Center Maastricht (CTCM)
    Clinical Trial Center Maastricht (CTCM)

    Clinical Trial Center Maastricht is de professionele ondersteuner van mensgebonden onderzoek. Samen met haar partners tracht het, om als toonaangevende Academische Research Organisatie, een waardevol wetenschappelijk resultaat na te streven.

    CTCM kan als partner fungeren voor iedere individuele onderzoeker, onderzoeksinstelling, of firma, op het gebied van mensgebonden onderzoek, variërend van monocenter tot multicenter onderzoek in heel Europa.

    Het uitgebreide pakket aan diensten omvat alle aspecten van ondersteuning voor mensgebonden onderzoek. Deze dienstverlening voldoet aan de hoogste kwaliteitsnormen en richtlijnen.

    Mw. V. van Wegberg v.van.wegberg@mumc.nl
    Website: http://www.ctcm.nl

  • Clinical Trial Service BV (CTS)
    Clinical Trial Service BV (CTS)

    Clinical Trial Service BV (CTS), founded in 1993, optimizes medical scientific research at strategic and operational level in the life science industry and healthcare. We are an innovative and dynamic CRO where dedicated research professionals are the basis for our services and products. We offer solutions focused on  increasing efficiency and quality. Our International Home Care Service where research nurses visit patients at home to perform clinical trial visits, results that patients stay longer in the trial and are more compliant. This service is unique and rated as excellent by the sponsors, sites and patients.

    Clinical Trial Service BV  is a full-service provider in medical scientific research in Europe:

    Submit clinical trials to Medical Ethics Committee and Competent Authorities for obtaining approval;
    Set up – execute – manage and monitor your clinical trials;
    Advice and Consultancy in setting up and carrying out your clinical trials;
    Training for investigators, research staff and teams in legislation and regulations such as ICH-GCP E6, ISO 14155: 2011, focusing on daily practice;
    Managing and Conducting of International Home Care Visits by research nurses;  nursing / medical procedures for clinical trials at patients’ home, in all European countries.

    Mrs. Mirjam J.P. Bruggink, founder and CEO mirjam.bruggink@clinicaltrialservice.com
    General company email address : contact@clinicaltrialservice.com
    Website: http://www.clinicaltrialservice.com

  • CR2O

    With headquarters in Amsterdam and Rotterdam, CR2O has built extensive experience managing and implementing phase I-IV clinical trials in over 30 countries and accumulated expertise through >400 studies over the last decade. We also have access to Ph-I units in Rotterdam and Nijmegen, where we are conducting our early stage work.
    Our therapeutic focus is oncology, vaccines, cancer immunotherapy, immunology, and autoimmune disorders. Through our network with several leading clinics and research centers in Europe we gain access to world-class scientific expertise and subject populations.
    Our experience and expertise includes scientific advice planning, clinical development consulting, feasibility studies, and the entire management of clinical trials, including data management, biostatistics, pharmacovigilance, quality management, medical writing. We could also support you with IMP handling and Central Laboratory management.
    Our unique combination of scientific expertise, operational efficiency and access to subjects make us an attractive partner for pharma, biotech and public organizations.
    To our customers, we are ‘the right size’ full service CRO. Our experience will save you valuable time and budget, allowing you to focus on what you do best.

    Dhr. N. van den Bulk nick.vandenbulk@cr2o.nl
    Dhr. R. Helmich rob.helmich@cr2o.nl
    Website: www.cr2o.nl

  • Diagram B.V.
    Diagram B.V.

    Diagram is a globally operating independent full service CRO able to support with the development, organisation and execution of clinical scientific research.

    The company was founded in 1996 in the Netherlands. In the past years, Diagram has acquired considerable expertise in supporting cardiovascular research, including trials performed in the ambulance (pre-hospital phase) and e-Health projects.

    Diagram’s quality management (NEN-EN-ISO 9001:2015 certified), strongly developed integrated ehealth and information management team, data management and statistics team, project management team and international focus, makes them different from other CRO’s.

    Diagram primarily focuses on Principal Investigators (so-called “investigator initiated studies”), start-up’s both in the Netherlands and abroad and the pharmaceutical-, medical device- and e-Health industries.

    Diagram deems a high quality level, including compliance and monitor timelines. In addition, the CRO plays a leading role in projects investigating new technological developments, such as e-Health, in a scientific setting.

    Mw. L. van den Brink-Drok: l.vdbrink@diagram-zwolle.nl
    Mw. S. Postma: s.postma@diagram-zwolle.nl
    Website: https://www.diagramresearch.com/

  • EAU Research Foundation
    EAU Research Foundation

    The EAU Research Foundation (EAU RF) was established in 2007, as an independent foundation.

    The EAU Executive Board acts as the foundationǯs Board of Trustees – this ensures close ties between the two organisations. The European Association of Urology currently provides most of the EAU-RF funding, enabling the foundation to perform independent research. Furthermore, this tight cooperation helps to align goals and to be consistent in the implementation of projects in the field of urology research.

    Dhr. dr. W.P.J. Witjes w.witjes@curatrial.com
    Mw. C. Caris c.caris@curatrial.com
    Website: https://uroweb.org/research/

  • EB Medical Research
    EB Medical Research

    EB Medical Research bestaat uit onze sites EB FlevoResearch in Almere en EBUtrechtResearch in Utrecht. Wij zijn een onafhankelijke medische onderzoekscentra welke geneesmiddelenonderzoek uitvoeren in opdracht van farmaceutische of andere bedrijven, ziekenhuizen of andere onderzoeksinstellingen. Bij EB Medical Research werken zo’n 10 professionals.

    Mw. B. Dormans b.dormans@flevoresearch.com
    Website: https://www.flevoresearch.com/

  • Emsere

    With offices in the Netherlands and in the United States, Emsere understands the needs of a clinical trial and delivers clinical trial equipment solutions to ensure their customers a full-service equipment experience. Emsere provides customers with proactive trial equipment solutions and manages those solutions with a single point of contact for all questions and support. Their global coverage with customs clearance and personalized study tracking of budget, inventory and delivery details provide exceptional, personalized service from study startup to study completion and all phases in between. Emsere’s equipment, supplies and software solutions extend to thousands of products, a rental fleet with over ten thousand devices and serving over 9,000 investigator sites to customers all over the world.


    Mw. C. Eilering caroline.eilering@emsere.com

  • GCP Central B.V.
    GCP Central B.V.

    GCP Central biedt online WMO/GCP trainingen aan farma, CRO, biotech en ziekenhuizen. We hebben de nieuwste inzichten over “mobile learning“ gecombineerd met onze kennis van wetenschappelijk onderzoek. Het resultaat? Modulaire, praktijkgerichte elearning in een modern en gebruiksvriendelijk design. Welke altijd en overal beschikbaar voor de cursist: via smartphone, tablet en PC. Of je nou CRA, onderzoeker, arts, verpleegkundige of een ander type research professional bent: Onze volledig online WMO/GCP training legt de Nederlandse wetgeving uit op een op jou toegespitste manier.

    Mw. M.A. Meulemans marieke@gcpcentral.com
    Website: http://www.gcpcentral.com

  • iClusion

    Clinical trials don’t just advance science; they also serve as in-the-moment treatment alternatives for patients.  iClusion aims to make trials more accessible for patients and their care-givers, and the clinical trial start-up process faster and more effective. Rather than each group remaining siloed, iClusion’s clinical study portal “Trial Eye” invites various stakeholders (study sponsors, research professionals in hospitals and their patients) to connect in a closed loop ecosystem. The footprint iClusion wants to leave on this planet is changing the lives of patients.


    Mw. H. Janssen hanneke.janssen@iclusion.com
    Dhr. R. Divendal roel.divendal@iclusion.com

  • ICON Clinical Research (UK) Ltd.
    ICON Clinical Research (UK) Ltd.

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I-IV clinical studies.

    In a highly fragmented industry, we are one of a small group of organisations with the capability and expertise to conduct clinical trials and development projects on either a local or global basis. We have the operational flexibility to provide development services on a stand-alone basis or as part of an integrated “full serviced” solution.

    We offer a full range of consulting, development and commercialisation services from a global network of offices in 37 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality –and our global team of experts has unparalleled experience in a broad range of therapeutic areas.

    Mw. M. Faber marije.faber@iconplc.com
    Mw. I. Boddeke ingeborg.boddeke@iconplc.com

    Website: http://www.iconplc.com

  • Intermark Technology ECG Research
    Intermark Technology ECG Research

    Intermark Technology ECG Research entered the market in 2015. The company is a spin-off from Intermark Technology that has over 25 years experience in Holter analyses for Dutch hospitals. Intermark Technology ECG Research is an independent GCP-compliant research organization. We specialize in quality Holter and ECG analyses services (e.g. HRV, thorough QT/QTc) to support pharmaceutical companies and Contract Research Organizations.

    Dhr. R.P. Steenbrink ronald@ecgresearch.com
    Website: https://www.ecgresearch.com/


    Quintiles en IMS Health zijn samengegaan en zijn vanaf november 2017 IQVIA, the #HumanDataScience Company™. Gedreven door de zorgsector die we helpen, zijn we gecommiteerd oplossingen te bieden die stakeholders in de zorg helpen vol vertrouwen te innoveren en het maximale uit opportuniteiten te halen. Met als ultieme doel bij te dragen aan betere uitkomsten voor de volksgezondheid. #WeAreIQVIA

    Mw. A. Boersen annette.boersen@iqvia.com
    Mw. A. Horn Arlette.Horn@iqvia.com
    Website: http://www.iqvia.com

  • Julius Clinical
    Julius Clinical

    Julius Clinical is a unique academic research organization (ARO) that combines strong scientific leadership and operational excellence to conduct innovative national and global clinical trials.

    Our partners include leading pharmaceutical, biotech, medical device, and food companies, as well as academic investigators. We focus on clinical trials that are likely to have a major impact on medicine and on peopleǯs lives. This type of demanding research requires more than a ‘one-size-fits-all’ approach, and our fusion of scientific and operational expertise enables to deliver results efficiently, on time and budget.

    Dhr. A. Bonefaas anton.bonefaas@juliusclinical.com
    Website: https://www.juliusclinical.com/


    KLIFO BV, formally MediServ, is a contract research organization, established in 1980 as the first of its kind in the Netherlands. KLIFO BV is part of the KLIFO group having its head office in Demark and another subsidiary in Germany. KLIFO BV covers The Benelux. Via the KLIFO group and PSN Research it has access to all European countries, North America and Canada. KLIFO is the service organization for the health industry: the one-stop contractor in clinical research.

    Contact person:
    Mw. Dr. O.B. Jochems info@mediserv.nl
    Website: http://www.mediserv.nl/

  • Labcorp

    Covance by Labcorp is a leading global life sciences company, which provides contract research services to the drug, medical device and diagnostics, crop protection and chemical industries.

    COVANCE is a registered trademark and the marketing name for Covance Inc. and its subsidiaries around the world.

    Covance by Labcorp is a leading contract research organization (CRO) that provides contract research services to the drug, medical device and diagnostics. Employing over 26,000 people worldwide, we provide comprehensive drug development solutions and are on a mission to advance health and power clear, confident decisions.

    Covance by Labcorp is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical, and regulatory expertise. Together with our clients, we support the development of innovative, life-changing treatments.

    Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions.

    Through our unparalleled diagnostics and research development capabilities, we provide insights and accelerate innovations to improve health and improve lives.

    With more than 75,000 employees, we serve clients in more than 100 countries.

    follow us on LinkedIn and Twitter @Labcorp.

    Our Mission

    To improve health and improve lives.

    Our Vision

    To be recognized by clients as:

    The undisputed leader in providing drug development services

    A trusted partner whose hallmarks are

    Great people

    High-quality data

    A proven track record of integrating and streamlining the development process

    Michiel Koeijvoets
    Senior Director Portfolio Oversight  Michiel.Koeijvoets@covance.com

    Maarten van Wieringen
    Senior Manager Global Quality Control  Maarten.VanWieringen@covance.com

    Ana Mercedes Valencia-Larrea
    Manager Clin Ops AnaMercedes.ValenciaLarrea@covance.com

  • LAP&P Consultants B.V.
    LAP&P Consultants B.V.

    Leiden Experts on Advanced Pharmacokinetics & Pharmacodynamics (LAP&P) is a consulting company offering Modelling and Simulation (M&S) Services to support decision making in Drug Discovery and Drug Development for pharmaceutical and biotechnological companies.

    We strive for further development and application of these techniques by actively participating in scientific research and contributing to education programmes. We also offer tailor-made courses.

    Dhr. H.J. Drenth, PhD h.drenth@lapp.nl
    Website: http://www.lapp.nl/

  • Link2Trials

    Link2trials is the independent website where volunteers (healthy volunteers and patients) can register to take part in medical research, pharmaceutical research, psychological research, nutritional research or the testing of medical devices and products. Researchers, from all over the world, can use this website to find and select suitable healthy subjects or patients for their research. At the same time they are able to place an advertisement of a clinical trial. Subjects (patients or healthy volunteers) are able to participate in different research projects.

    Dhr. S. Klaasen simonklaasen@link2trials.com
    Website: https://www.link2trials.com/

  • Medpace

    As a global leader in research-based drug and medical device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to approval. As a therapeutically-focused Contract Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents.

    Mw. A.M. Saarloos
    Mw. R. Lila
    Website: http://www.medpace.com/

  • MRI Centrum (St. MRI Diagnostiek)
    MRI Centrum (St. MRI Diagnostiek)

    Conducting research in the MRI Center

    The MRI Center conducts MRI research at one of its own locations according to the established protocol for the trial concerned by order of the researcher / CRO, for instance for the benefit of Alzheimer and MS research. We offer a fast trial startup and short lines of communication. We have ample experience as a partner in researchprojects and have been collaborating with various researchers, pharmaceutical companies and CROs for years. Our radiologists are very experienced and they ensure that they remain up to date, initiate research and stimulate the sharing of knowledge and information.

    Dhr. C.H. Falkenström chehsin.falkenstrom@mricentrum.nl
    Mw. N. Schuur nelleke.schuur@mricentrum.nl
    Website: http://www.mricentrum.nl/

  • OCS Life Sciences
    OCS Life Sciences

    OCS Consulting’s specialist business unit OCS Life Sciences has been supporting clients with data analysis and reporting, business intelligence, data management and data integration since 1998. Clients are diverse ranging from pre-clinical, vaccines, medical devices, nutrition, academia and, of course, traditional pharmaceutical companies.

    The core competencies of our OCS Life Sciences practice are based on the needs in clinical research for (Bio) Statistics, Statistical Programming, CDISC standardisation, Data Science and Clinical Data Management support.

    OCS Life Sciences consists of a multidisciplinary team of data specialists with an academic background in science or IT. Our consultants are very keen on working with scientific data and we share this passion with our clients.

    Yves Poriau
    Melanie Schopp
    Jules van der Zalm
    Website: http://www.ocs-lifesciences.com

  • Parexel Nederland B.V.
    Parexel Nederland B.V.

    For over 30 years, PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. Weǯre also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly.Headquartered near Boston, Massachusetts, PAREXEL operates in 82 locations in 51 countries around the world, and has 18,450 employees.

    We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, integrated eClinical technologies, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.

    Mw. E. De Raeve mailto:els.deraeve@parexel.com
    Dhr. P. Rietman peter.rietman@parexel.com>

  • Pharmacokinetic Consultancy Services (Erelid)
    Pharmacokinetic Consultancy Services (Erelid)

    Pharmacokinetic Consultancy Services (PCS) is an independent consultancy company, located in the Netherlands with extended experiences and active in the following areas:

    Pharmacokinetic advise
    Project management
    Special formulation advise
    QA audits and management
    Medical writing and publications
    Training courses
    Regulatory advice

    Dhr. P.J.M. Guelen pharmacokinetics@home.nl
    Website: http://www.pharmaconsultancy.nl/

  • PPD (Netherlands) B.V.
    PPD (Netherlands) B.V.

    PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 15,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health.

    Mw. J. Soer janet.soer@ppdi.com
    Mw. M. Eppens marjolein.eppens@ppdi.com
    Mw. N. Oesterholt nicole.oesterholt@ppdi.com
    Website: http://www.ppdi.com/

  • PRA Health Sciences
    PRA Health Sciences

    The story of PRA Health Sciences would naturally talk about how weǯve become one of the worldǯs largest CROs. It would talk about our innovation and growth and would speak to our operational efficiencies and transparency. It would highlight our expertise and customization. And it would touch on the incredible differences we’ve made, over our more than 30 years, in helping to bring to market everything from niche treatments and therapies to blockbuster drugs.

    More than anything else, our story would be about people. Not only our over 11,000 employees operating in more than 80 countries, though theyǯd certainly be a big part of it, but also the people that inspire them. The heroes of any PRA Health Sciences story are the clients we serve and the people whose lives we help improve, all over the world. And our story has only just begun.

    View Our 2015 Sustainability Report

    Dhr. L. van den Broek vandenbroekluc@prahs.com
    Dhr. H. van der Meulen vandermeulenhans@prahs.com
    Website: http://prahs.com/

  • PT&R

    PreCare Trial & Recruitment (PT&R) is een onafhankelijke medisch onderzoekscentrum dat onafhankelijk klinisch wetenschappelijk onderzoek uitvoert. Dit betreft meestal onderzoek met nieuwe geneesmiddelen of voedingssupplementen die nog in een ontwikkelings- en onderzoeksfase zijn of onderzoek naar nieuwe toepassingsgebieden van bestaande middelen. De onderzoeken worden uitgevoerd in opdracht van farmaceutische of voedingsmiddelenbedrijven, andere onderzoeksinstellingen, (academische)ziekenhuizen of overheden.

    PT&R werkt bij het uitvoeren van wetenschappelijk onderzoek samen met huisartsen, patiënten en vrijwilligers. Teneinde u van de juiste informatie te voorzien, kunt u een keuze maken uit een van bovenstaande opties.

    Mw. V.E.K.M. van de Walle vivienne.vandewalle@ptr.nu
    Website: http://www.ptr.nu/Home/

  • QPS Netherlands
    QPS Netherlands

    Founded in 1995, QPS is a GLP/GCP-compliant contract research organization (CRO) supporting discovery, preclinical and clinical drug development. We provide quality services to pharmaceutical and biotechnology clients worldwide.

    Dhr. Dr. R. Schwietert reinier.schwietert@qps.com
    Dhr. Dr. W.J. Tamminga wim.tamminga@qps.com
    Dhr. Dr. J. Wieling jaap.wieling@qps.com
    Dhr. I. den Daas

  • Research drive B.V.
    Research drive B.V.

    Research Drive BV is a CRO located in the northern part of the Netherlands. Our team of clinical research professionals and monitors are dedicated to ensure the best outcome of our clients’ clinical trials. In the past two decades, we have managed studies on behalf of more than 80 different clients, which include  Pharma, Biotech, Medical Device, and Nutritional companies, Clinical Pharmacology Units, and University/ Top Clinical Hospitals.

    Our expertise includes management and monitoring of complex first in human, feasibility, and Phase I and II studies. We have built knowledge and expertise in a wide variety of therapeutic areas and our team is widely trained to adapt quickly to new innovative areas.

    We provide services in the Netherlands and Belgium, and we have also team with field-based staff throughout Europe.

    Mw. J. Beukema j.beukema@researchdrive.com
    Website: http://www.researchdrive.com

  • Saberg Clinical Research
    Saberg Clinical Research

    Saberg Clinical Research is a full service CRO which combines exceptional scientific knowledge with innovative research techniques. We focus our collaboration on start-up and small-medium size biotech and pharmaceutical companies which develop novel compounds or medical devices. Our aim is to become an “extension” of our Sponsors’ teams through a highly pro-active approach of their needs and our outstanding availability. We cover a wide range of therapeutic areas and development phases with a focus on cardiovascular, diabetes, neurology and hematology.

    Dhr. S. Bergheanu sandrin.bergheanu@saberg.org
    Website: www.saberg.org

  • Siron Clinical BV
    Siron Clinical BV

    Siron Clinical: Because experience matters

    We’ve set our brand expectations high.

    We aim to be the highest quality and most experienced expert CRO of choice for small and medium-sized biotechs navigating complex European clinical research.

    How do we do it? Our business focuses on 3 core values: Quality, Reliability,  and No-nonsense.

    1. Quality

    It always has, and always will be a top priority for the business and brand. We believe in nothing less, and it lays the foundations for our whole organization.

    2. Reliability

    We know we can make a difference and bring new medicines faster to those in need. That’s why trust and transparency are paramount to the success of our patients, trials, investigators, clients, and partners.

    3. No-nonsense

    For the last 20 years, we’ve been operating a systematic, no-nonsense approach to clinical operations, because we know time is of the essence when it comes to saving lives. We act with compassion, respect, and care. We nurture relationships and projects to build brighter, healthier futures.

    Siron Clinical offers expertise for clinical trials throughout Europe, Israel and Turkey.

    Dhr. J.A.M. Balemans         j.balemans@sironclinical.com
    Mevr. W. Meijst                    w.meijst@sironclinical.com
    Website:                                 https://www.sironclinical.com/

  • SMS-oncology

    Clinical trials are all about obtaining valuable data to show proof of concept, protecting patients and compiling the regulatory dossier, but developing anticancer drugs is a complex business. The right expertise is required to navigate the best way forward. Imagine availing of in-depth knowhow and receiving proactive guidance from oncology trial design to full execution. This will not only give you a head start, but will also allow you to be on top of your data, make informed decisions, mitigate risks and identify opportunities during study conduct.

    Offering an integrated approach of clinical operations with expert advice, SMS-oncology sets itself apart from typical CROs by providing Direction during the entire Drug-Data-Dossier path. With our unique “4D” service we are able to give you meaningful insights that will contribute to the successful development of your oncology compound.


    Mevrouw E. Verheijen e.verheijen@sms-oncology.com
    Mevrouw J.P.  van den Tol p.vandentol@sms-oncology.com
    Mevrouw C. de Jong-Evegaars officemanager@sms-oncology.com

  • Syneos Health
    Syneos Health

    Syneos Health™ (Nasdaq:SYNH) is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies – INC Research and inVentiv Health – we bring together more than 23,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. To learn more about how we are shortening the distance from lab to life® visit syneoshealth.com.

    Dhr. G. Veerman gveerman@syneoshealth.com
    Mw. A. Claessens Angela.Bodewes-Claessens@syneoshealth.com
    Mw. T. van der Galiën trea.vandergalien@syneoshealth.com
    Website: https://www.syneoshealth.com/

  • TAPAS Group B.V.
    TAPAS Group B.V.

    The TAPAS Group is a team of 5 highly experienced experts in the field of clinical research. Each member has over 20 years experience in all aspects of research including freelance consulting. We believe that Clinical Research can be best facilitated by managing studies according to clear, relevant and standardised processes by using transparent communications and by the employment of adequately trained personell. This belief is reflected in our way of working.

    Mw. T. Lemmens tooslemmens@tapasgroup.com
    Dhr. N. Riegman nicoriegman@tapasgroup.com
    Website: http://www.tapasgroup.com/?lang=nl

  • TFS Trial Form Support B.V.
    TFS Trial Form Support B.V.

    TFS is the leading global mid-size clinical Contract Research Organization. For comprehensive, clinical development services, TFS offers the highest level of competence, experience and personal attention to ensure we achieve the best results for our customers. With our suite of offerings, our customers’ clinical trials will be handled with care and expertise.

    TFS is in the business of improving and refining the delivery of better healthcare outcomes to ensure our customers’ successes. We genuinely believe that being GLOBAL IN MIND AND LOCAL AT HEART is the core of our success; our customers know TFS’ in-depth knowledge about regulatory and clinical trial requirements in every country, ensures a global trial will move faster to market and result in shorter timelines to get treatments to the patients who need them.

    Mw. L. Brugmans Linda.Brugmans@tfscro.com
    Dhr. R. Dijkerman rembrandt.dijkerman@tfscro.com
    Website: http://www.tfscro.com/

  • The Clinical Company
    The Clinical Company

    The Clinical Company specializes in delivering Clinical Services in The Benelux to our (Bio)Pharmaceutical, Medical Devices and CRO Clients. We are known for our skilled and motivated clinical professionals and the quality of our services. Our Clinical Services include Project Services, Contract Staffing and Recruitment Services.

    Our Clients include global top 30 pharma companies as well as small and midsized CRO, Medical Devices and Biotech organisations.

    Founded in 2002, The Clinical Company became known under its current name in 2010, opening offices in Amstelveen, The Netherlands and Brussels, Belgium in 2011. With a current staff of close to 40 clinical professionals based in The Benelux, The Clinical Company will remain focused on the quality and stability of its services by ensuring the quality of its staff, its procedures and the work enjoyment of all of its employees.

    Mw. A. Kleemans mailto:a.kleemans@theclinicalcompany.com
    Website: http://www.theclinicalcompany.com/

  • Up Strong
    Up Strong

    Up Strong aims to facilitate Business Strategy & Management in Life Sciences, to truly innovate and work for what really matters … the patient needs!

    We assist with challenges in the following areas with a strong focus on the human side of the drug development cycle:

    • Training & coaching (communication, feedback & conflict resolution high-performance teams; change management; Lean-based solutions implementation; Golden Circle implementation)
    • Business Strategy (business case development/strategy; vendor selection process; business development support)
    • Patient Engagement (patient landscape mapping, co-creation clinical trials/recruitment strategies, online pre-screening/patient companion service)
    • (Interim-)Management (business operations, business development, executive management & project management)

    Towards true innovation to make our industry more societally acceptable and sustainable!

    Dhr. R.J. Legtenberg
    Website: http://www.up-strong.com

  • Venn Life Sciences
    Venn Life Sciences

    Venn Life Sciences is an Integrated Drug Development Partner offering a unique combination of drug development expertise and clinical trial design and execution. This enables us to create, plan and execute drug and medical device development programs effectively and seamlessly for our clients.
    We have dedicated operations in Ireland, France, Germany, the Netherlands, the UK, the US, and Europe-wide representation.


    Mw. M.E.A. van den Dobbelsteen
    Website: www.vennlifesciences.com

  • WCN

    WCN (Werkgroep Cardiologische centra Nederland) network is a dedicated group of experienced cardiologists and well-trained research professionals from nearly 60 non-academic hospitals across the Netherlands. Since the network’s foundation in 1988, WCN has collaborated with many pharmaceutical and medical partners in a variety of clinical trials. The network is a reliable partner, with a proven track record and experts in our field. Quality is one of our priorities and our effective processes allow for an efficient enrolment. WCN positions itself as a key player in the field of clinical research and as the representative of all associated cardiovascular institutes in the Netherlands.

    At WCN we are driven by heart.


    Mw. A. Schut
    Website: www.wcn.life

  • Your Research
    Your Research

    Your Research is an innovative digital platform that enables researchers via apps to remotely involve patients interactively in research, to carry out appointments with patients digitally and remotely and to communicate with researchers and study sites. The platform was created in collaboration with UMC Utrecht and now supports more than 25,000 patients in dozens of studies.

    Your Research is een innovatief digitaal platform waarmee onderzoekers via apps op afstand patiënten interactief kunnen betrekken bij onderzoek, afspraken met patiënten digitaal en op afstand kunnen uitvoeren en kunnen communiceren met onderzoekers en studie sites. Het platform is tot stand gekomen in samenwerking met het UMC Utrecht en ondersteunt inmiddels meer dan 25.000 patiënten in tientallen onderzoeken.

    Kees van Ooik
    Website: www.yourresearch.com

Lid worden van de Acron?

Mocht u lid willen worden van de ACRON, dient u zich te registreren. Sinds 1 december 2014 verplicht de ACRON alle leden zich te registreren via de “toetsing en registratieprocedure” van de ACRON. Onderdeel van deze procedure zijn een vragenlijst en de acceptatie van de Code of Conduct van de ACRON. Het doel dat de ACRON nastreeft met deze zorgvuldige
procedure is om als branchevereniging toonaangevend te zijn op het gebied van kwaliteit van medisch wetenschappelijk onderzoek en daarmee de ideale gesprekspartner te zijn voor beleidmakers binnen onze branche.

Wanneer u zich wilt registreren, dient u het formulier compleet in te vullen. U ontvangt dan op korte termijn, mits uw aanvraag gehonoreerd wordt, een e-mail met login gegevens voor het afgeschermde ACRON registratie domein. Binnen dit domein zijn alle benodigde documenten en de vragenlijst en toetsingscriteria beschikbaar. Uw definitieve aanvraag dient vervolgens binnen 4 weken compleet te zijn ontvangen door de ACRON. De toetsing- en registratiecommissie van de ACRON beoordeelt vervolgens uw aanvraag, waarna het bestuur u hopelijk mag verwelkomen als nieuw lid. Mocht U vragen hebben dan kunt U contact opnemen met het ACRON secretariaat.


De klachtencommissie is een onafhankelijke commissie binnen de ACRON. Noch het bestuur, noch de ALV is gemachtigd invloed uit te oefenen op de commissie.  Het bestuur is niet betrokken in de klachtenprocedure. Alleen klachten binnen Nederland en anders dan fraude worden behandeld door de klachtencommissie.

De uitslag van de klachtencommissie is bindend, er is geen beroepsmogelijkheid.

Meldingen kunnen gestuurd worden naar klachtencommissie@acron.nl


Heb je vragen over ACRON? Neem eenvoudig contact met ons op.