Partners

Cmed is developing key partnerships with selected consultants, CROs and technology vendors to provide our customers with the best level of service and product capabilities available. Our partners are established players in their respective fields and together we offer solutions that will both streamline and enhance the end-to-end clinical development process.

To visit partner websites please click on the logos below.

ACRO

ACRO (African Clinical Research Organisation) is based in South Africa and was established to meet the ever-increasing demands of the global biotechnology sector, donor-funded organisations, non-governmental organisations, research institutions, pharmaceutical and medical device companies and government institutions, who are looking for a clinical research organisation that is cost-effective, and able to offer locally priced solutions to international standards, whilst assuring the highest standard of ethics and quality across all service offerings.

ACRO and Cmed have partnered to deliver full service offerings in Africa.

Argint International

Argint International Clinical Research and Development Services (Argint) is a privately owned, regional CRO based in Central and South Eastern Europe (CEE/SEE). Argint provides cost-effective clinical research and regulatory outsourcing solutions to pharmaceutical and biotech companies. Argint combines personal service, flexibility and local expertise with the knowledge of what is required to effectively manage global clinical trials.

Argint and Cmed have partnered to deliver full service offerings in Eastern Europe.

Berry Consultants

Berry Consultants is a statistical consulting group specializing in adaptive clinical trial design in pharmaceutical and medical device research and development. They are leaders in the Bayesian approach to medical statistics. This approach is radically changing the way research is done throughout the medical industry (device and drug development). They employ world renowned experts in Bayesian statistics and strive to set the standard for Bayesian design and analysis in the statistical and medical communities.

Charité Research Organisation

The Charité Research Organisation (CRO) is a Contract Research Organization that has been established with one objective in mind – to better serve the unique needs of the early clinical development community than any organization before it. Based in Berlin, the CRO was founded in collaboration with Berlin’s famous Charité University Hospital. This relationship fosters a level of cooperation with centres of clinical excellence that we think is unique in the industry.

Charité Research Organisation and Cmed have partnered to deliver full service offerings in an early phase setting.

Formedix

Formedix is a leading provider of software and consultancy services based on emerging data standards developed by CDISC, (Clinical Data Interchange Standards Consortium). Formedix delivers CDISC software and services that have resulted in time and cost savings in every key area of the clinical trial process from study set-up through to submission.

Formedix’s technology suite is fully integrated with Timaeus, facilitating rapid study set-up and CDISC implementation.

IBM

Today’s healthcare and life sciences industries face unprecedented demands: reducing clinical and administrative costs – meeting tighter compliance and security mandates – harnessing an explosion of data – accelerating drug discovery and development – creating targeted treatments -improving the quality of diagnostic decisions.

IBM is the premier Clinical Development system integrator and business consulting, help desk and hosting partner. It can provide the technology, services, consulting and e-business experience needed to meet these demands and realise new opportunities in an ever-changing environment.

Tessella

For over 25 years Tessella has worked with some of the biggest names in the pharmaceutical industry. It helps clients address a wide range of business goals, including, improving efficiency and productivity in drug discovery, delivering the business benefits of translational medicine, and faster more effective clinical trials.

Biosoteria

Cmed and BioSoteria have partnered to provide our clients with the broadest range of drug safety services in the biopharmaceutical industry. BioSoteria is a full-service Pharmacovigilance Services Provider with an experienced team of practitioners who can help clients monitor and risk manage the safety of their products with a regulatory-compliant, best pharmacovigilance practices approach. With an experienced management team, each more than 20 years or more of relevant experience, they have an established record of regulatory compliance and are seen as leaders in the industry, contributing to industry best practices in clinical safety surveillance, post marketing pharmacovigilance and therapeutic risk management. BioSoteria’s integrated pharmacovigilance solutions and individually tailored services for clients provide our clients with the best breadth of services and leadership in the pharmaceutical industry.

CMED Associations