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Electronic data capture system

for any type of clinical investigation

Are you looking for
a preconfigured EDC system?

Simply provide us
with study Protocol and CRF and

you will receive
a ready-to-go system
to collect clinical data

OnlineCRF provides as
a protocol-
base
preconfigured tool

We know that no two projects are alike. Significant variability of study designs puts a high pressure on the person who is responsible for selecting a proper data collection tool. Software development companies strive to create very flexible tools for clinical investigations. However, the more flexible they become, the more challenging such system is to implement. Our team has found an elegant solution: to use your protocol and CRF and provide you with a fully configured EDC system.
Read more

Expert opinion
The Fastest
Growing Business
Apps Discovery Platform

OnlineCRF is an intelligent and efficient EDC system purpose-built for small and medium teams to assist them in managing simple and complex projects. It is equipped with tools for real-time project tracking that are accessible from the dashboard to allow the swift and live monitoring of trial dynamics. This also enables researchers to avoid bottlenecks in the study.

With OnlineCRF, you also have access to real-time validation of inputted values. The system automatically initiates the checking function as soon as numbers are entered. If it encounters an error, the user is notified immediately for the prompt rectification of the data. As such, you are assured of the quality of information you have for the success of your trials.

Moreover, OnlineCRF provides unparalleled flexibility. You can have a wide range of variations and modifications in the program, especially when you have a particular functionality that you need. OnlineCRF works with you in that regard to ensure that the software adapts to your needs.

https://reviews.financesonline.com/p/
onlinecrf/

OnlineCRF fits
a variety of trial and study designs
Clinical Trials
I-IV phase
  • Randomized/non- randomized;
  • Blinded/unblinded;
  • Stratified;
  • Comparative, crossover;
  • Single or multi-country
Postmarketing studies
Non-interventional
  • Observational, epidemiologic, retrospective;
  • Large-scale: up to 300 sites, up to 50 000 subjects;
  • PAES, PASS, DUS;
  • Single or multi-country
Registries
Long term projects
  • Disease registries;
  • Product registries;
  • Medical device registries
Need more details?
We will conduct a tour and give you advice of how to design a project and what aspects should be taken into account before the study begins
References

"Pharmaxi LLC maintains the high professional level of personnel and clear processes aimed at goals achievement. We recognize Pharmaxi LLC as a trustworthy partner with a responsible attitude to their obligations and consider them to be a team of experts in the profile activity. We recommend Pharmaxi LLC as a reliable and stable business partner."

Alla Gontar,
Medical Head

"We’ve been working with Pharmaxi since 2014 in frame of epidemiological multicentre study in Ukraine and the Baltic countries in the field of hepatitis C. We are satisfied with the work of the team that demonstrates the high level of professionalism and quality in the design and management of clinical databases.”

Galyna Bryn,
Ukraine & CIS Medical manager

Our Company has been collaborating with Pharmaxi team since February 2017. During this period Pharmaxi has been providing us with a wide range of services related to maintenance and update of information in corporate electronic systems within a company’s clinical operations. Our projects require a good organization and a high level of communication skills, as well as attention to the details and respect of agreed timelines. A dedicated Pharmaxi team is assembled according to our specific needs and ensure adequate quality with the implementation of internal quality checks performance. We feel a high engagement, professionalism, accuracy and client orientation that is critically required for the success of every particular project.

We are pleased to recommend Pharmaxi as a qualified, well-managed and reliable partner for the tasks performance related to the electronic systems and data collection management.

Serhiy Mykhaylov, M.D., MBA
CRD Ukraine, Georgia & CIS
OnlineCRF features
Secured access
Only authorized person has access to data
Data
pre-validation
Before data is saved to the database, it is checked against applicable ranges. Invalid data will not be saved to DB
Digital Signature
Principal investigator can sign CRFs which have been populated and checked
OnlineCRF complies
with the industry standards
Immediate advice from
our expert

A free 30-minutes consultation with our data managers, project managers or statisticians. You will get an efficient advice on how to create your study design or clinical data collection approach and where to focus your efforts today.

No cost or obligations.
Answer all relevant questions

Our beloved clients
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