Menu Close

Exhibitor List

Exhibitor and Sponsor List

All exhibitors and sponsors of the 2018 ACDM Annual Conference will have their description, contact details and logo displayed in the format shown below. 


Brookwood is in its 32nd year and is well known as a provider of global clinical research training, both online and face to face. At this conference we will be showcasing our brand new online, on demand data management training module together with our new book, A Guide to GCP for Clinical Data Management. The book and training cover the key ICH GCP E6(R2) requirements relevant to members of the data management team. They also provides valuable practical advice gained from the author’s extensive experience in this field. Come and see us and find out more at our exhibition stand. You can even ask for online access to evaluate the course.

Brookwood’s well known online narrated Essential GCP training for both sponsors and investigators  is available in 11 languages – it meets TransCelerate minimum requirements for the mutual recognition of GCP training for investigators and has been passed by over 30,000 users globally.

Canary specialises in producing books, newsletters and teaching aids to facilitate global regulatory compliance, particularly good clinical practice (GCP) and Pharmacovigilance (PV).


Find us at Stand Number: 1


PRA Health Sciences

PRA Health Sciences is an award winning CRO.

We are proud to have won Pharma Times ‘Clinical Research Company of the Year’ in 2017 for the fourth consecutive year. We aren’t winning these awards by chance; PRA is being recognised industry-wide for our dedication to the future of clinical development. Most importantly for you, at PRA we recognise that our success is down to our people.

At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do.  We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.


Find us at Stand Number: 3




Established for more than 26 years, IDDI (International Drug Development Institute) provides quality clinical data ready for submission, thanks to a unique combination of methodological excellence and operational efficiency.


Increase efficiency and mitigate risks throughout your clinical development by using IDDI, your CDISC Registered Solutions Provider.



IDDI has a broad expertise in various therapeutic areas and a special focus in oncology, ophthalmology, CNS, metabolic, cardiovascular, auto-immune, infectious diseases and rare diseases.

Our experience spans 26+ years with 900+ trials and 17 FDA/EMA approvals to-date.

IDDI is based in Belgium – EU, with offices in Cambridge MA, Raleigh NC, San Francisco CA, USA. .


Find us at Stand Number: 2



Viedoc by PCG Solutions is a global EDC and ePRO vendor with offices in Sweden (Uppsala), Japan (Tokyo) and China (Shanghai). Viedoc is a modern and future-proof EDC that allows clinical trial sponsors and study sites to easily and securely collect, validate, transmit and analyze clinical study data.  

Viedoc is a proven software since 2003 which meets or surpasses all regulatory benchmarks. Designed to be as intuitive as possible, Viedoc saves time and frustration from users at every level, allowing clinical trial organizations to have more focus on their own innovation and leadership.


Find us at Stand Number: 4


Keyrus Biopharma

Keyrus Biopharma is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.

At Keyrus Biopharma we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better

From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.


Find us at Stand Number: 5



Excelya is a Contract Research Organisation (CRO) that provides services for biotechnology  and pharmaceutical companies,  medical devices and cosmetics firms. Our scope of intervention concerns trials from Phases I to IV. We are working for most of the ten top largest pharmaceutical companies in the world. At Excelya, we do consider that retaining our employees ensures their professional development and provides the best service level to our clients. These are key factors for our success, and our company values.


Find us at Stand Number: 6



EDGE provides an innovative cloud-based clinical management system that empowers frontline clinicians to make the most of their research data. EDGE is specifically designed to give a real-time view of clinical research activity within a single hospital or network within the UK, Canada and beyond. EDGE was developed by the Clinical Informatics Research Unit (CIRU) within the Faculty of Medicine at the University of Southampton. CIRU operates as an applied research and enterprise unit working nationally and internationally with the core aim and vision to transform clinical research and practice through novel approaches to information and software management.

E: Twitter: @EDGEclinical

Find us at Stand Number: 7



PHASTAR is a specialist CRO offering statistical consulting and clinical trial reporting services to the pharmaceutical industry. Our number one priority is to ensure the work we produce is of the highest quality: every project PHASTAR undertakes is supervised on methodology and utilises unique internal processes designed to ensure the best quality. Our aim is to provide a service that is ahead of our competitors: in the last 2 years, we have been involved in the design and reporting of over 200 studies, and each has delivered on-time and with no quality issues. We can provide data collection as a MEDRIO partner. Talk to us about using MEDRIO for your study – MEDRIO is fully functional, easy to use, and sensibly priced.


Find us at Stand Number: 8



CluePoints® is a Risk-Based Monitoring and Central Statistical Monitoring solution that has been designed and perfected over the last 15 years. It employs unique statistical algorithms to determine the quality, accuracy, and integrity of clinical trial data both during and after study conduct. Aligned with guidance from the ICH, FDA and EMA, CluePoints® is deployed to support traditional on-site monitoring, medical review and to drive a Risk-Based Monitoring strategy.


Find us at Stand Number: 10



Quanticate is a leading global Data-focused Clinical Research Organization (CRO) primarily focused on the management, analysis and reporting of data from clinical trials and post-marketing surveillance. As Experts in Clinical Data, Quanticate provides high quality teams that offer efficient outsourcing solutions for clinical data management, biostatistics, SAS programming, statistical monitoring medical writing and pharmacovigilance.  Quanticate can offer study level support, functional service provision (FSP), strategic full data-services solutions or technical consultancy to meet the needs of pharmaceutical, biotechnology and device companies across the globe.  By offering high quality, value-add client specific solutions to meet current and future development needs, Quanticate has become the supplier of choice for many companies from Top tier pharmaceutical giants through to niche biotechnology and device companies


Find us at Stand Number: 9


Arithmos srl

Arithmos is an ISO 9001 and ISO 270001 certified IT company focused on Life Sciences industry.

Our solutions support multiple clinical trial processes enhancing efficiency and global alignment:

  • Electronic Data Capture: Symphony EDC is an intuitive SaaS EDC solution designed by investigators and developed by Arithmos to allow a quick and autonomous study set up and management, fully in compliance with international standards;
  • Clinical Trial Management: SYNClevy is and Extended Project and Portfolio Management system developed to support clinical project managers in their daily activities’ planning and management, increasing collaboration among all company’s departments and enhancing Clinical Trial Oversight, as required by ICH GCP E6(R2);
  • Pharmacovigilance: Argus Blueprint is a pre-configured, fully validated pharmacovigilance platform for the fast deployment of Argus Blueprint.


Come meet our experts at Arithmos Booth


Find us at Stand Number: 11


Castor EDC

Castor EDC is making medical research faster and smarter with their user-friendly data capture platform. They provide a mobile-friendly EDC for clinical trials, built by researchers, for researchers. Features include self service eCRF creation (form building), randomization, ePro (patient surveys), monitoring, easy import and export of data, EHR data importer (HL7 FHIR based), audit trails, user management, and much more. We are fully ISO 27001 certified, GCP, 21 CFR & GDPR compliant and provide servers in the US (HIPAA compliant), the Netherlands and the United Kingdom.


Find us at Stand Number: 12