Since 1997 CROMSOURCE has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting quality and client focus at the heart of everything we do.
At CROMSOURCE we live by our motto – Advise, Agree, Deliver. This means we leverage our experience and expertise at the early stages of discussions with our clients to freely advise them on the optimal project plan. We then reach agreement with each client on the scope of service, timelines and budget.
CROMSOURCE then commits to delivering those services on-time and within budget – according to our End-to-End Guarantee. Our commitment to guaranteed delivery is unique in the clinical research environment which is otherwise notable for the routine occurrence of delays and cost overruns.
Acting through our expert 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 program, through to provision of full services to a pharmaceutical company performing an international trial 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 within the agreed timelines.
CROMSOURCE is committed to providing flexible services to support every aspect of our clients’ needs. To learn more about our comprehensive services and problem solving approach please visit our website and select a service area: ttps://www.cromsource.com/services/
CROMSOURCE has embraced, developed, and invested heavily in technology relating to clinical research. This resulted in the formation of our associated company and wholly-owned subsidiary, Techorizon Srl (www.th-clinical.com).
We believe that technological innovation is essential to streamlining workflow, enhancing decision making, and improving the quality and efficiency of clinical trials. By remaining at the forefront of creating and developing ground-breaking technological solutions, our experts help us deliver faster, efficient services and allow our teams to work smarter and faster on your projects.
The new TheClinical 3.0. delivers enhanced functionality in a fully-integrated environment. From the feasibility study to the final study report, this platform offers many solutions for each stage of a clinical trial.
By means of PC, tablet or smartphone, all services are securely accessed with the use of the most advanced encryption standards available today.
Through our TalentSource Life Sciences division, CROMSOURCE continues to lead the way in providing flexible staffing solutions. With more than 22 years of experience 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 organization.
CROMSOURCE has been active in the Central Eastern European area since its inception in 1994, and has enormous experience in these regions. CROMSOURCE has an extensive European infrastructure and operates subsidiaries in Germany, Spain, Belgium, Poland, Ukraine, Russia, the UK, the Netherlands and the USA. These subsidiaries, and our field-based staff located in many other European countries provide an established infrastructure where CROMSOURCE is active across all of Europe and the USA.
Offices in: Belgium, Germany, Italy, Poland, The Netherlands, Spain, UK, Russia, Ukraine
Los Angeles, CA
Put simply, One Trial One Price is our unique pledge that the price agreed at contract signature is the only price that the client will pay. CROMSOURCE provides our clients with a concrete budget which contrasts markedly with the change order culture prevalent in today’s CRO industry. It is the embodiment of the CROMSOURCE commitment to deliver high quality data to our clients on time and on budget.
CROMSOURCE believes that a rigorous assessment of country and site level feasibility is critical to trial success and must be implemented early in trial planning. Without detailed and accurate feasibility data on which to base country and site selection, a reliable prediction of enrollments rate and therefore successful planning of trial milestones is impossible. If your last trial was delayed by recruitment issues, you may wish to consider the level of detail you were provided with in the feasibility assessment.
Working closely with our sponsors, CROMSOURCE identifies those geographic areas well known for their prevalence of the targeted indication. All regulatory requirements are then reviewed and timeliness developed for each country to ensure fast regulatory approvals.
CROMSOURCE then works directly with the most professional and productive sites in every area of the world. Sites are only considered if they have proven they can deliver a combination of high enrollment, high retention, and quality data. Each site is requested to identify potential patients far in advance of study start-up, thus assuring there are no surprises during the enrollment phase.
Quality data. On time. On Budget. Guaranteed.
At CROMSOURCE we believe experts should keep their word. After 18 years of success in supporting our clients to meet their clinical research goals we have a solid history and experience with highly productive geographies, sites, investigators and regulators. We are so confident in our abilities to deliver your study on time and on budget that we are able to offer the industry’s only End-to-End Guarantee.
Starting at the RFP stage with our uniquely detailed Feasibility PlusTM process (delivered free and without obligation) we ensure that we provide realistic predictions of enrollment and timelines, and recommend the right mix of countries and sites. Our End-to-End Guarantee then covers the following areas:
Furthermore, we know that budgets must be competitive, and you can rest assured that our End-to-End guarantee does not come with a premium price. Don’t you owe it to your project to learn more? Contact us here to request more information.
Is your current trial is running behind schedule, or you would like support from a CRO who are experts in rescuing such studies? If so, CROMSOURCE can help!
We know where the patients are and how to enroll them. We know which countries have the highest prevalence of various diseases and the sites that consistently deliver the highest volume of qualified patients.
And because we monitor competing studies in all major markets we help our sponsors understand the competitive landscape. We then advise them to avoid those countries and re-direct them to markets with the patients needed to finish their study on-time.
Finally, a sponsor’s rescue study may qualify for our End-to-End Guarantee. If your study meets certain requirements we will guarantee not only the specified number of patients but also the date of database lock.
To ask how we can help bring your study in on-time, click here.