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Cmed Clinical Services

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Cmed Clinical Services

Cmed is a full-service, global contract research organisation that specialises in the design and delivery of early Phase I to IIb patient clinical trials. Cmed is increasingly being asked to deliver existing client’s phase III studies, as well as provide standalone solutions across all its services, including biometrics functional services.

Biopharmaceutical support services

Cmed responds to the current challenges faced by the biopharmaceutical industry, with specialist capabilities and expertise, readily available to support the industry through the design and operational delivery of innovative and/or complex early Phase I to IIb clinical trials.

Cmed accomplishes this through deep regulatory and medical insight, superior drug development consulting, robust clinical operations, in-depth biometrics solutions, as well as Timaeus (our in-house eClinical technology).

Cmed’s size allows flexibility, experienced project oversight, innovation, priority, as well as comfort and security.

Cmed has successfully delivered more than 400 traditional and innovative Phase I and II trials:

  • Complex oncology studies and programmes
  • Proof of concept
  • Adaptive designs
  • Complex translational medicine studies
  • Evolutionary CRF designs
  • First in human, patient, PK and dose escalation
  • Wide ranging therapeutic pedigree

Cmed’s reputation of partnership mentality is based on trust, transparency and common goals:

  • Repeat business greater than 90% from more than 30 clients
  • Early phase oncology preferred provider for major pharmaceutical company
  • Translational medicine preferred provider for a biopharmaceutical company
  • Long-term partnerships with numerous pharma and biopharmaceutical companies
  • Design and delivery of award winning innovative projects

Cmed operates from offices in the UK, US and Romania and has been involved in delivering studies in many therapeutic areas across numerous countries worldwide.

Contact details

Cmed Clinical Services
Worldwide Head Office
Holmwood, Broadlands Business Campus,
Langhurstwood Road
Horsham, West Sussex
RH12 4QP
United Kingdom
Phone: +44(0) 1403 755050
Fax: + 44(0) 1403 755051
Email: info@cmedresearch.com
Website: www.cmedresearch.com

Quick Contact Cmed Clinical Services


Biometrics Consulting

Cmed’s biometrics consulting group was created when the need for well-founded advice and senior-level support in the industry arose.

Our cross-functional experts boast between ten to 20 years' experience in many indications, and work with companies of all sizes to help address the biometrics challenges they face on a daily basis.

Biometrics Functional Service Provision

With biometrics core to our business, we are proud to have developed and maintained FSP strategic relationships over the years.

The FSP models we already have in place include:Biometric strategic partners for the early phase (translational medicine)Biometric preferred providers for early phase oncology adaptive trialsBiometric preferred provider for Phase IV trials

Biostatistics

Cmed’s biostatistical team comprises of experts within the pharmaceutical sector and contract research organisations. Our biostatistical team are highly knowledgeable, with senior-level statisticians bearing an overall average of more than 15 years’ experience.

This team provides innovative statistical design and analysis opportunities, with a great understanding of flexibility, as well as the importance of delivering timely and high-quality products.

Clinical Monitoring

Clinical research associates (CRAs) are the vital link between the site and the project team.

Cmed's network of CRAs consists of highly experienced individuals, providing the benefit to our clients of not having junior or inexperienced CRAs monitoring their clinical trials.

Data Management

Cmed’s data management team has delivered cost-effective clinical data management services and solutions using innovative technology for more than 13 years.

Cmed's highly experienced team has the capacity of a large contract research organisation, but with the benefits provided by a mid-sized company, such as client-tailored solutions (e.g. budget, resource, location and systems).

Drug Safety

Cmed offers lifecycle safety management of products, spanning from clinical development all the way through to post-marketing.

With our collective experience, we can provide a fully-inclusive approach to safety reporting on a global-scale. What's more, our experienced safety management experts can be integrated as part of a full-service Cmed or sponsor team.

Medical Affairs and Monitoring

Success of medical affairs during a clinical study can be achieved through a blend of operational excellence, technology and medical oversight.

Cmed's team of medics cover the full range of medical affairs expertise which any clinical project may require.

Medical Affairs & Drug Safety

Cmed's medical affairs and drug safety team are here to assist you during all phases of your product development lifecycle, from drug to device and concept to post market, and here to take the stress and guess work out of safety and risk management.

Medical Device Consulting

Cmed helps medical device companies develop new products through:

Innovating - Cmed formulates the environment for innovation to grow in the face of increased competitionDeveloping - Cmed finely-tunes product and process development as well as marketing and regulatory capabilitiesCommercialising - Cmed accelerates the time-to-market of new and unique productsMaximising value - Cmed increases the market place value of existing and new products

Medical Writing

Cmed’s medical writers work closely with our other in-house disciplines to deliver accurate, suitable, and cost-effective clinical development documents to the highest ethical and scientific standards.

Project Management

Cmed offers clinical project management (PM) services from our North American and European locations.

Project management for clinical trialsEach PM is assigned to a project by closely aligning their experience and knowledge with the project requirement.Although Cmed's area of expertise is Phase I to IIb patient clinical trials, our PM expertise extends to Phase III to IV, across the majority of therapeutic areas.

Regulatory Affairs

Cmed's global regulatory services are organised into two categories: operations and strategic consulting.

OperationsCmed's global regulatory team provides continual support to start-up clinical projects quickly and efficiently, in accordance with regulatory conditions.Strategic consultingStrategic consulting consists of a combination of regulatory knowledge, experience as well as a strong understanding of business and industry practices, in order to support and improve the complete product development cycle, from R&D and proof-of-concept,…

Risk Based Monitoring

With every clinical trial unique, Cmed works alongside with each of our clients to assign a specific clinical monitoring strategy to their study.

The eClinical technologies we have in place offer a complete array of information and metrics which enable the project team to analyse within and across sites for particular trends, outliers and signals.Consequently, key decisions are allowed to be made with regard to ongoing monitoring strategies. Following this, we use a combination of onsite and remote…

Strategic Advice

Cmed’s experts are knowledgeable in all areas of product development, and assist the biopharmaceutical industry through clinical development and regulatory strategies which provide maximum product value, either upon marketing approval or via out-licensing.

Quick Contact Cmed Clinical Services
Quick Contact Cmed Clinical Services
Quick Contact Cmed Clinical Services


Quick Contact Cmed Clinical Services
Quick Contact Cmed Clinical Services
Quick Contact Cmed Clinical Services


Contact Cmed Clinical Services

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