PureCDM specialises in the provision of Clinical Data Management services and deployment of eClinical solutions to Biopharmaceutical and MedTech companies with products in of all phases clinical development.
We are a software neutral service provider guaranteeing that our clients get a truly tailored solution that fits with product development goals and budget.
Our mission is to maximize the value of clinical trial data and to support faster "Go/No-Go" decisions by making data accessible when required.
We have a flexible approach to clinical data management services and can provide the full suite of data management services and oversight, or act as consultants supporting various data management functions as required.
The team have an average of 20 years of cross-functional expertise and 'know-how' to manage all data management aspects of a trial.
PureCDM team members have extensive experience in clinical development across several therapeutic areas including;
In addition we have extensive experience in phase 1 dose escalation and expansion safety studies and understand the flexibility and data accessibility that is required during the execution of these studies.
Our team members and strategic partners have considerable experience with many industry leading EDC systems.
PureCDM has been a great partner in developing useful clinical data for our Phase 1b/2a trial. The experts at PureCDM have core expertise that was instrumental in constructing the right database from our clinical trial design. They are a critical piece in our accelerating US based drug development program and an important part of our success to date. I highly recommend them.
The PureCDM team demonstrated seamless data management skills, customer-focus and flexibility. The team was a joy to work with (even under difficult circumstances!)
The team at PureCDM have tremendous in depth knowledge of the data management field, and a great ability to understand what best meets the needs of different companies and different projects. Additionally, their broad knowledge and experience of other functional areas involved in drug development is a major asset. I would have no hesitation in recommending the team at PureCDM to anyone looking for efficient and cost-effective data management solutions.
I have had the pleasure of working with PureCDM on several projects. The PureCDM team are very aware of client needs and keeping those in line with project budget and time expectations.
I had the pleasure of working with PureCDM over a two-year period. I was working at a small start up with no in-house data management, and PureCDM functioned as our virtual data management team. They understand the needs of start-up companies very well, and form an excellent partnership. We took their advice on the database platform to use and we were not disappointed. Their project management team is efficient, excellent with communication, and met every timeline.
I highly recommend PureCDM!
Pure CDM is Easington's preferred data management service provider. Helen and her experienced team consistently establish user friendly systems, produce high quality results on time and on budget in compliance with client requirements and regulatory guidelines. They are proactive, responsive, flexible and always willing to help if issues arise. It's a pleasure working with them.
M2M has worked with PureCDM for the last 5 years across a variety of clinical trials where they have provided data management services to the studies we manage. The knowledge, experience, flexibility and enthusiasm they bring to the table has facilitated each of our studies to be completed on time, on budget and to the highest quality. Our shared values of honesty and integrity, coupled with their dependability and professionalism make PureCDM a great asset to the conduct of a successful clinical trial.
Helen Poliviou, Managing Director at PureCDM, has over 24 years of experience in pharmaceutical development gained through working with academic research institutions, global Clinical Research Organisations (CROs), Pharmaceutical Companies as well as the smaller entrepreneurial business sector across various functions.
As Director of Operations, Rachel Greaney is responsible for overseeing all operational activities within the company. She has over 22 years of data management and clinical research experience working within Clinical Research Organizations (CROs), Pharmaceutical Companies and within the not for profit hospital system.