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- - Pharmaceutical
    - - Acting through Pharmaceutical, Medical Device and Staffing Solutions teams, and with a comprehensive portfolio of services, we offer a flexible approach to ensure CROMSOURCE optimally support the unique needs of each client. This could mean providing regulatory consultancy to a small company at the early stages of a medical device development programme, through to provision of full services to a pharmaceutical company performing an international megatrial to support registration of their product. Whatever the size and scope of the project, each receives the same level of attention to detail and commitment to delivery of a high quality service within budget and to timelines agreed.
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  - Medical Devices
    - - The CROMSOURCE Medical Device team knows and understands medical device and diagnostics regulations; most of the staff has been through the regulatory process for clinical trial and product approval in the USA and EU many times. Therefore our operational team understands the regulatory implications of its actions and decisions, so your clinical study or regulatory submission is in safe, expert hands. We are also able to offer our clients the benefit of a large collective experience when formulating and implementing regulatory strategies and study designs, and CROMSOURCE’s mid-size and flat management structure means that this experience is not lost within a vast organisation.
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  - Biometrics
    - - CROMSOURCE is an expert partner for Clinical Data Management, Statistics and Medical Writing projects. In the past 15 years the Biometrics group within CROMSOURCE has conducted hundreds of important projects either as part of full-service agreements or as stand-alone assignments. We consistently delight our clients by proactively searching for the most efficient solution to their needs. Since our success is founded on repeat business from satisfied clients, you can also be sure of the highest quality and customer service from CROMSOURCE. We enjoy helping our clients to reach their goals, and hope we have the chance to do the same for you.
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  - Early Phase
    - - When choosing a partner for your early phase clinical projects, you need an expert. For many years the CROMSOURCE Early Phase facility formed the Phase I unit of a top 10 global pharmaceutical company. When this company disinvested in the facility, it moved location to the nearby teaching hospital, taking the expert team and cutting edge equipment with it. In 2012 it became the CROMSOURCE Early Phase facility. Our sponsors can therefore be certain that the quality and expertise of our facility is second to none.
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  - Flexible Resourcing Solutions
    - - Through our TalentSource Life Sciences division, CROMSOURCE continues to lead the way in providing flexible staffing solutions. With over 20 years experience of providing high quality clinical research professionals, we are able to add real value to your work by allowing you to efficiently adjust the size of your team to peaks in workload. We are equally comfortable acting in a functional service provider setting or in simply providing short and long term or permanent staff for your organisation.
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CROMSOURCE Regulatory Newsletter July – September 2018

CROMSOURCE announces publication of its latest Regulatory Newsletter summarising important

CROMSOURCE Appoints Director of Regulatory Services and Expands Regulatory Operations

CROMSOURCE announced today the appointment of its Regulatory Services Department Director,

CROMSOURCE Regulatory Newsletter April – June 2018

CROMSOURCE announces publication of its latest Regulatory Newsletter summarising important

CROMSOURCE Unveils New TalentSource Life Sciences Department Logo

CROMSOURCE announced the formalisation of an expanded Flexible Resourcing Solutions

CROMSOURCE Regulatory Newsletter January – March 2018

CROMSOURCE announces publication of its latest Regulatory Newsletter summarising important

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Via Giorgio De Sandre, 3
37135 Verona – Italy
Phone +39 045 8222811
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309 Waverley Oaks Road, Suite 101
Waltham, MA 02452 – USA
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