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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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Posts

CROMSOURCE Regulatory Newsletter January – March 2016
OmniComm Systems Signs Five-Year, Multi-Million Dollar TrialMaster EDC Agreement with CROMSOURCE
CROMSOURCE Expands Operational Footprint and Management Team
CROMSOURCE Regulatory Newsletter Special US Edition – June 2016
Changes to EU Medical Device legislation – What you need to know – White paper, 2016
CROMSOURCE Expansion Medical Services CMO
TalentSource Article – CRA Perspective of Medical Device Studies
TalentSource Article CRA Perspective on Interviewing
CROMSOURCE Regulatory Newsletter July – September 2016
CROMSOURCE Regulatory Newsletter October – December 2016
CROMSOURCE Continues Strong US Growth with Multiple New Business Awards
CROMSOURCE Regulatory Newsletter January – March 2017
CROMSOURCE Celebrates its 20th Anniversary
CROMSOURCE Regulatory Newsletter April – June 2017
CROMSOURCE EU Medical Device Regulation
CROMSOURCE Regulatory Newsletter July – September 2017
CROMSOURCE Regulatory Team to Present at TOPRA’s Clinical Evaluation of Medical Devices Masterclass
Partnership In Clinical Trials
Outsourcing in Clinical Trials Medical Devices USA 2018
TOPRA Annual Medical Devices Symposium 2017
Outsourcing In Clinical Trials West Coast 2018
Outsourcing In Clinical Trials Medical Devices Europe 2018
CROMSOURCE Regulatory Newsletter October – December 2017
CROMSOURCE Offers Clients One Trial One Price™ Guarantee
CROMSOURCE Regulatory Newsletter January – March 2018
CROMSOURCE Unveils New TalentSource Life Sciences Department Logo
CROMSOURCE Regulatory Newsletter April – June 2018
CROMSOURCE Appoints Director of Regulatory Services and Expands Regulatory Operations
CROMSOURCE Regulatory Newsletter July – September 2018
Partnerships in Clinical Trials Europe
Outsourcing in Clinical Trials: Medical Devices Europe – 6th-7th February 2019
CROMSOURCE Regulatory Newsletter October – December 2018
CROMSOURCE Regulatory Newsletter January – March 2019
CROMSOURCE Regulatory Newsletter April – June 2019
Penta and CROMSOURCE Announce their Partnership to Improve Paediatric Drug Development
CROMSOURCE Continues US Growth with New Office in Research Triangle Park
CROMSOURCE Consolidates its Hybrid Services Model
CROMSOURCE Regulatory Newsletter July – September 2019
CROMSOURCE announces a significant milestone in digital management of its projects in cooperation with TECHORIZON
CROMSOURCE Announces Launch of COVID-19 Clinical Trial
CROMSOURCE Regulatory Newsletter January – March 2020
CROMSOURCE Regulatory Newsletter April – June 2020
CROMSOURCE Regulatory Newsletter July – September 2020

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About CROMSOURCE

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One Trial One Price
End-to-End Guarantee
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European Headquarters:

Via Giorgio De Sandre, 3
37135 Verona – Italy
Phone +39 045 8222811
Fax +39 045 8222812

North America Headquarters:

309 Waverley Oaks Road, Suite 101
Waltham, MA 02452 – USA
Phone +1 617 871 1128
Fax +1 617 871 1129

ISO 9001:2015 multi-site certified quality management system
ISO 14155:2011 conformity confirmed

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