Annual Conference 2017 Exhibitors Information


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ACDM Sponsors/Exhibitors 2017

The ACDM gratefully acknowledges the support of our sponsors and exhibitors


Covance Inc.
As the drug development business of Laboratory Corporation of America Holdings (LabCorp) and the world’s most comprehensive drug development service company, we have helped pharmaceutical and biotech companies develop each of the top 50 prescription drugs in the marketplace today. Because of our broad experience and specialized expertise, we’re in a unique position to supply insights that go above and beyond testing. Together with our clients, we create solutions that transform potential into reality.

Kubo Recruitment

Kubo Recruitment 
Kubo Recruitment is a global recruitment company focused on sourcing talent in the Life Sciences sector. We only match candidates that fit the job requirements and the work environment. Our areas of recruitment focus are clinical research, clinical data management, statistics and programming, pharmacovigilance, medical affairs, clinical monitoring and IT.


Lambda-Plus sa nv
Through fully integrated Data Management, Biostatistical and Medical services Lambda-Plus offers eClinical Trial services guaranteeing the highest quality of clinical trials data and outputs resulting from a streamlined process from protocol to clinical study report.

Using FLeX+ proprietary eClinical system Lambda-Plus eClinical experts build intuitive e-Platforms integrating eCRF, IWRS and ePRO intuitive solutions to support interventional trials and non-interventional studies.

Linical is a Silver Partner of Oracle, the market leader in EDC technology, for the Enterprise adoption of its EDC (InForm) Solution. All operational and build activities are conducted by Linical's experienced EDC personnel. Moreover, Linical has become an industry Partner of the American Society for Clinical Data Management (SCDM).


Medsharing, created in 2000, is headquartered in France and provides EOL©, a 100% internet SaaS eClinical eCRF software solution for clinical trials, epidemiology, surveys and AEs management across Europe and beyond. EOL© is 21 CFR Part 11 validated, and the company is ISO 9001 certified. EOL© is hosted in France by a Healthcare French Ministry agreed hosting company.

Oracle Health Sciences
Oracle Health Sciences is a leading strategic software solutions provider to pharmaceutical, biotechnology, medical device and healthcare organizations. We are transforming clinical R&D from pipeline to patient, helping organizations improve patient outcomes by providing actionable insights from aggregated clinical and healthcare data while optimizing clinical trial efficiency and productivity.
phastar Phastar
PHASTAR is a specialist CRO offering statistical consultancy, clinical trial reporting and data management services, by providing expert consultants and delivering in-house projects. Our number one priority is to ensure that the work we produce is of the highest quality: every project PHASTAR undertakes is supervised on methodology and utilises internal processes designed to ensure optimal quality. Services include production of clinical study reports including generating tables, figures and listings; study design and protocol writing; modelling and simulation; and advice on handling missing data across phase I to IV trials. Our headquarters is in Chiswick, London (UK) with additional offices across four continents. We partner with pharmaceutical and biotech companies globally. 
PRA Health Sciences
At PRA Health Sciences, providing innovative solutions for our clients is what we do. Side-by-side with our clients, we strive to move drug discovery forward, helping them to develop life-saving and life-improving drugs. With our unique blend of expertise, we provide comprehensive clinical development services across all phases. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.
As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 60+ such drugs.
The XClinical Software Solution Marvin comprises a CDISC-certified EDC system that integrates with numerous modules such as Randomization, Patient Reported Outcomes, Double Data Entry, Clinical Trial Management, CDISC Tabulation, Reporting, Coding and more to manage the complete lifecycle of a clinical study in one single integrated solution.