Leden van de ACRON

Op dit moment zijn 44 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

    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.

    Contactpersonen:
    Dhr. E. Oosting eoosting@abl.nl
    Dhr. K. de Jonge kdejonge@abl.nl
    Website: www.abl.nl

  • 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.

    Contactpersonen:
    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

  • Auxiliis – Pharma
    Auxiliis – Pharma

    Auxiliis is a full service Contract Research Organisation (CRO), dedicated exclusively to paediatric clinical trials. We understand the ethics of care for this vulnerable population and have wide experience of paediatric trial design and execution. As a result, we can ensure that the young participants benefit from medical progress without being exposed to unnecessary risks. With more than 50 paediatricians in-house and a Central East Eurpean network of 200 paediatricians we can call upon at any time, our paediatric expertise is extensive and highly varied.

    We offer a new approach to paediatric clinical trials. We use our experience to manage all aspects of your proposed paediatric trials – designing the research, implementing the trials, and submitting the final research reports for review by regulatory authorities.

    Contactpersonen:
    Dhr. W. Wijker wouter.wijker@auxiliis-pharma.com
    Dhr. O. Skoran otto.skoran@auxiliis-pharma.com
    Website: http://www.auxiliis-pharma.com

  • BiKE
    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.

    Contactpersonen:
    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

     

  • 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.

    Contactpersonen:
    Dhr. Prof.dr. A.F. Cohen ac@chdr.nl
    Dhr. Prof.dr. J.M.A. van Gerven jvangerven@chdr.nl
    Mw. R. Kroon rk@chdr.nl
    Dhr. Dr. P. Peeters rk@chdr.nl
    Website:
    http://www.chdr.nl

  • Chiltern International BV
    Chiltern International BV

    Contactpersonen:
    Mw. W. Wuyster winnifred.wuyster@chiltern.com
    Mw. H.A. Boering hellen.boering@chiltern.com
    Website: http://www.chiltern.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.

    Contactpersonen:
    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 (CTS) optimaliseert medisch wetenschappelijk onderzoek op strategisch en operationeel niveau binnen de life science industrie en gezondheidszorg. We zijn een innovatief en dynamisch bedrijf, waarbij toegewijde professionals de basis vormen voor onze diensten en producten. Wij bieden oplossingen gericht op het verhogen van efficientie en kwaliteit.

    Contactpersonen:
    Mw. M.J.P. Bruggink mirjam.bruggink@clinicaltrialservice.com
    Dhr. M. Hagmanns marcel.hagmanns@clinicaltrialservice.com
    Website: http://www.clinicaltrialservice.com

  • ClinTec International ltd
    ClinTec International ltd

    ClinTec International is a full service clinical research organisation, operating in 40 countries. we offer a broad range of services. Operating in the Netherlands for over 15 years, ClinTec International has vast clinical experience in the country.

    KEY SERVICES IN THE NETHERLANDS:

    Clinical monitoring and site management Large-scale functional resourcing Project management Patient enrolment and retention services Consulting

    Contactpersonen:
    Mw. M. de Jong-de Haan mdjong@clintec.com
    Website: http://www.clintec.com/locations/europe/netherlands

  • Curve Clinical B.V.
    Curve Clinical B.V.

    Curce Clinical B.V. conducts early stage clinical studies, as well as specialized later stage studies, across a broad range of therapeutic areas with a particular focus in oncology, vaccines, cancer immunotherapy, personalized medicine and autoimmune disorders.

    Contactpersonen:
    Dhr. N. van den Bulk nick.vandenbulk@curveclinical.com
    Dhr. R. Helmich rob.helmich@curveclinical.com
    Website: www.curveclinical.com

  • Diagram B.V.
    Diagram B.V.

     

    Diagram (Diagnostic Research and Management) is een ISO 9001 gecertificeerde research organisatie, bestaande uit twee bedrijfseenheden: Contract Research Organisatie/Corelab (CRO/Corelab) en Site Management Organisatie (SMO)

    Diagram is een full service CRO voor de ontwikkeling en organisatie van klinisch wetenschappelijk onderzoek. Onze teams faciliteren het gehele traject van onderzoeksopzet tot en met eindrapportage.

    Diagram richt zich op individuele onderzoekers (Principal Investigators) in topklinische en universitaire ziekenhuizen in binnen- en buitenland en op de farmaceutische-, medical device- en eHealth industrie.

    Diagram heeft in de afgelopen jaren veel expertise opgebouwd op het gebied van cardiovasculaire ziekten en longziekten. Daarnaast speelt zij een voortrekkersrol bij projecten die nieuwe technologische ontwikkelingen, zoals eHealth, in een wetenschappelijk setting onderzoeken.

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

  • Dinox
    Dinox

    Dinox is een CRO op het gebied van de gynaecologische endocrinologie en houdt zich bezig met klinisch geneesmiddelenonderzoek.

    De artsen bij dinox zijn al meer dan 25 jaar werkzaam in dit vakgebied. Dinox wordt in Europa gezien als een uniek expertisecentrum. Het team heeft lange tijd uitsluitend uit vrouwelijke artsen, verpleegkundigen en doktersassistenten bestaan, maar in de laatste jaren zijn er twee mannelijke collegaǯs bijgekomen.

    Dinox is gevestigd in de voormalige kliniek interne geneeskunde op het UMCG terrein in Groningen en heeft daar eigen bedrijfsruimten: spreekkamers, onderzoekkamers met echoapparatuur, ruimtes voor bloedafname, verwerking en opslag van bloedmonsters en opslag van onderzoeksmedicatie. Voor de meeste onderzoeken bij dinox zijn slechts korte bezoeken noodzakelijk en is het niet nodig dat je blijft overnachten. Voor onderzoeken waarbij wel overnachtingen nodig zijn, wordt samengewerkt met “collega” CRO’s.

    Contactpersonen:
    Dhr. A. Beynon a.c.beynon@dinox.umcg.nl
    Mw. I. Duijkers i.j.m.duijkers@dinox.umcg.nl
    Mw. C. Klipping c.klipping@dinox.umcg.nl
    Mw. A. Remmers a.remmers@dinox.umcg.nl
    Website: http://www.dinox.nl/

  • 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.

    Contactpersonen:
    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.

    Contactpersonen:
    Mw. I. van Welsen I.vanWelsen@emotionalbrain.nl
    Mw. A. Boersen A.Boersen@emotionalbrain.nl
    Website: https://www.flevoresearch.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.

    Contactpersonen:
    Mw. M.A. Meulemans marieke@gcpcentral.com
    Mw. I. Boddeke ingeborg@gcpcentral.com
    Website: http://www.gcpcentral.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.

    Contactpersonen:
    Mw. M. Faber marije.faber@iconplc.com
    Mw. D. Portocarero Diana.Portocarero@iconplc.com
    Dhr. T. Huizenga theo.huizenga@iconplc.com

    Website: http://www.iconplc.com

  • INC Research
    INC Research

    INC Research is een toonaangevende wereldwijde contract research organisatie (CRO) die het volledige scala van fase I tot fase IV klinische onderzoeksdiensten levert voor de biofarmaceutische en medische industrie sinds 1998. De CRO heeft haar hoofdkantoor in Raleigh, North Carolina en heeft ongeveer 6.400 medewerkers verspreid over zes continenten met ervaring in meer dan 100 landen.

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

  • InterEuropa Clinical Research BV
    InterEuropa Clinical Research BV

    InterEuropa Clinical Research BV 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.

    Contactpersonen:
    Dhr. S. Bergheanu sandrin.bergheanu@intereuropa.org
    Website: http://www.intereuropa.org/

  • InVentiv Health Clinical
    InVentiv Health Clinical

    inVentiv Health offers best practices, processes and systems to enable biopharmaceutical clients to successfully navigate an increasingly complex operating environment. We have more than 14,000 healthcare professionals servicing clients in 90 countries. We’ve directly supported nearly 60 percent of all drugs approved by the FDA in recent years. This includes about 70 percent of all approved new molecular entities – more than two-thirds of truly novel drugs. So, we have the proven model to help drive your product successfully from lab to life.

    Contactpersonen:
    Dhr. T. van Exsel twan.vanexsel@inventivhealth.com
    Mw. M. Kappert marion.kappert@inventivhealth.com
    Website: http://www.inventivhealth.com/

  • JPMB Consulting
    JPMB Consulting

    JPMB Consulting verricht ontwikkelingswerk voor klinisch onderzoek.

    Contactpersonen:
    Dhr. J.P.M. Blank john@jpmbconsulting.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.

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

  • Kinesis Pharma B.V.
    Kinesis Pharma B.V.

    Kinesis Pharma B.V. is an international operating consultancy and contract research organization (CRO) with headquarters in Breda (1997), the Netherlands and a regional office in Singapore (2010).

    Since October 2015 Kinesis Pharma B.V. is a member of Venn Life Sciences, a European Clinical Research Organisation providing clinical trial management and resourcing solutions to pharmaceutical, biotechnology, medical device and academic organisations. With dedicated operations in France, Germany, the Netherlands, the UK and Ireland and Europe wide representation –Venn specialises in multi-site cross cultural clinical trials with unique knowledge of local and EU regulations.

    Contactpersonen:
    Dhr. K. Groen Kees.Groen@kinesis-pharma.com
    Mw. S. Broekhoven simone.van.broekhoven@kinesis-pharma.com
    Website: http://www.kinesis-pharma.com/venn.html

  • 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.

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

  • Link2Trials
    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.

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

  • MediServ
    MediServ

    MediServ is an independent contract organization, established in 1980 as the first of its kind in the Netherlands. Today MediServ covers The Benelux and via PSN Research, all European countries, North America and Canada. MediServ is the service organisation for the health industry The one-stop contractor in clinical research.

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

  • Medpace
    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.

    Contactpersonen:
    Mw. A.M. Saarloos
    Dhr. R.H.A. Lohmann
    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.

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

  • OCS Life Science Solutions
    OCS Life Science Solutions

    OCS Consulting’s specialist business unit OCS Life Science Solutions 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 Science Solutions 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 Science Solutions 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.

    Contactpersonen:
    Yves Poriau
    yves.poriau@ocs-consulting.com
    Yasemin Atil
    yasemin.atil@ocs-consulting.com
    Melanie Schopp
    melanie.schopp@ocs-consulting.com
    Jules van der Zalm
    jules.vanderzalm@ocs-consulting.com
    Website: http://www.ocs-consulting.com/nl

  • 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.

    Contactpersonen:
    Mw. C. Vermeulen corien.vermeulen@parexel.com
    Dhr. P. Rietman peter.rietman@parexel.com>
    Website:
    https://www.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

    Contactpersonen:
    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.

    Contactpersonen:
    Mw. J. Soer janet.soer@ppdi.com
    Dhr. J.M. Kroodsma jan-maarten.kroodsma@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

    Contactpersonen:
    Dhr. R. Koning Koning Ronald@prahs.com
    Dhr. R. Nijssen NijssenRick@prahs.com
    Website: http://prahs.com/

  • PSR Group B.V.
    PSR Group B.V.

    PSR provides staffing solutions (PSR Pharma Resource) as well as Regulatory & Clinical Consultancy and Clinical Study Execution (PSR Orphan Experts). PSR is a leading expert in orphan drug development and are specialized in complex development clinical programs requiring innovative regulatory and clinical approaches. In the end we are about making a positive impact on the lives of people with rare diseases!

    Contactpersonen:
    Dhr. R. Legtenberg roger.legtenberg@psr-group.com
    Website: http://www.psr-group.com/

  • PT&R
    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.

    Contactpersonen:
    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.

    Contactpersonen:
    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
    Website:
    https://www.qps.com/

  • QuintilesIMS
    QuintilesIMS

    QuintilesIMS (QI) is a leading global healthcare provider of integrated information and technology-enabled services. QI is dedicated to helping its clients improve their clinical, scientific and commercial results. Formed through the merger of Quintiles and IMS Health, QI’s approximately 50,000 employees conduct operations in more than 100 countries. QI develops and implements solutions to help its clients maximize innovation and drive healthcare forward. To learn more, visit www.quintilesims.com

    Contactpersonen:
    Mw. C. Eilering Caroline.Eilering@Quintiles.com
    Mw. A. Horn Arlette.Horn@quintiles.com
    Website: https://www.quintilesims.com/

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

    Since its founding in 2004, Research Drive has been providing clinical trial services to pharmaceutical, biotech and medical device companies. Our dedicated team can manage your clinical trials efficiently throughout Europe, supported by our qualified assurance staff. Our flexible organizational structure and customer focus allow us to respond quickly to your project needs, ensuring a fast study start-up.

    With our headquarter based in the Netherlands, our affiliate in Belgium and field-based staff throughout Europe we cover clinical trial services in:

    • Austria
    • Belgium
    • Denmark
    • France
    • Germany
    • Hungary
    • Italy
    • Poland
    • Spain
    • Sweden
    • Switzerland
    • The Netherlands
    • UK

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

  • Robarts Clinical Trials BV
    Robarts Clinical Trials BV

    Robarts Clinical Trials is headquartered in London (Canada) with offices in La Jolla (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 and the analysis, interpretation and reporting of results.

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

    Contactpersonen:
    Dhr. H. Hoogeveen hans.hoogeveen@robartsinc.com
    Mw. M. Lammers merel.lammers@robartsinc.com
    Website: https://www.robartsclinicaltrials.ca/

  • Siron BV
    Siron BV

    Siron: Your partner in clinical outsourcing services

    SIRON BV is an independent contract research organization (CRO), equipped and organized to support, coordinate and manage clinical research projects in an efficient, solid and cost-effective manner.

    SIRON BV and its partners offers expertise for clinical trials throughout Europe, Israel and Turkey and have been able to serve business partners in the pharmaceutical industry, biotechnology/life sciences and medical devices.

    Since 2000, we have worked on the different phases of studies (proof of concept, phase I to phase IV, observational and registry studies), including regulatory services and in a wide variety of indications. Over the years, we have gained extensive experience in orphan disease studies, pediatric studies, and studies incorporating medical devices.

    Contactpersonen:
    Dhr. J.A.M. Balemans jan@sironeurope.com
    Website: https://www.sironeurope.com/

  • SMS-oncology
    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.

    Contactpersonen:

    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

  • 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.

    Contactpersonen:
    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.

    Contactpersonen:
    Mw. P. Matthijsse Petra.Matthijsse@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.

    Contactpersonen:
    Dhr. C. Jong c.dejong@theclinicalcompany.com
    Website: http://www.theclinicalcompany.com/

  • Venn Life Sciences
    Venn Life Sciences

    Venn Life Sciences is a European Contract Research Organisation providing drug development, clinical trial management and resourcing solutions to pharmaceutical, biotechnology, medical device and academic organisations. With dedicated operations in France, Germany, the Netherlands, the UK and Ireland and Europe wide representation – Venn specialises in rapid deployment and management of multi-site cross cultural clinical trials with unique knowledge of local and EU regulations. Over our 25 year history we have built up substantial therapeutic and study experience, contributing to the efficient management of sites, budgets and communication channels with all parties involved. Venn is renowned for its hands-on approach and consistent delivery of high quality work on time and on budget.

    Contactpersoon:

    Mw. G.A.M. Schutjens gracielle.schutjens@venncro.com
    Website: http://www.vennlifesciences.com/

  • WCN

    The Dutch Network for Cardiovascular Research (WCN) is an independent network of cardiology clinics in the Netherlands. As an established partner for all major pharmaceutical companies, the WCN conducts clinical trials in cardiovascular medicine.

    Founded in 1988, the Working group on Cardiovascular research the Netherlands (WCN) is an independent network organization of 57 cardiac clinics in The Netherlands. The WCN is an established partner to major pharmaceutical companies in the area of clinical research. All WCN clinics have academic research backgrounds and are widely experienced in international trials. As an organization, WCN monitors implementation of Good Clinical Practice and quality control. The WCN aims (1) to perform multi-centre clinical research in cardiovascular medicine for the pharmaceutical industry, non-profit research institutes and clinical research organizations, and (2) to be an associate in these projects from initial trial design up to the final details of execution, including ethics and regulatory affairs.

    Contactpersonen:

    Mw. A. Schut a.schut@wcnnet.nl
    Website: https://www.wcnweb.nl/

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.

Klachtencommissie

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

Contact

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