Try the most convenient way of Data-Export!
The main purpose of implementing Clinical Trial is to gathering Safety & Effectiveness Data, and this Dataset means everything for Clinical Trial. Unfortunately, so far conducting parties have had to get through some inconvenience & inefficient way to export Dataset in appropriate format, because no EDC solutions have provided in-house exporting system but cubeCDMS.
cubeCDMS, developed by CRScube Inc. and now in service with highly recognizable status in North-East Asian Clinical Trial society is equipped with powerful Data-Exporting System, and it provides following features;
1. Real-time Dataset Export
2. Various downloadable format(SAS, Access, Excel, CSV)
3. Available to reflect both Domain or Labal to Excel format.
This brings huge convenient point to its users by allowing them to export Clinical Dataset without using any of external programs.
Furthermore, CRScube is now planning to upgrade this exporting system, dramatically cutting SAS file size by reducing unnecessary end spaces. plus, cubeCDMS will support to export in XPT format very soon. For more information, please contact email@example.com
The cubeCONSENT is coming.
We at CRScube would like to introduce our most recent solution soon slated to join our other offerings of eclinical solutions: cubeCONSENT.
As its name suggests, cubeCONSENT is a solution which will enable the informed consent process as well as its oversight to occur electronically.
Specifically, using cubeCONSENT via a smartphone application, patients will be able to review the informed consent and give their consent via an electronic signature; principal investigators will be able to countersign a patient-signed consent form and return its copy to the owner; and sponsors will be able to oversee and manage the entire process with the aid of helpful visual metrics and analytics.
All of this is to ensure a streamlined, well-managed, and transparent informed consent process as well as to contribute to the long term inspection-readiness and overall quality of your clinical trial.
So please stay tuned for more announcements regarding a release date, or contact us today for more information at firstname.lastname@example.org.
WHODrug CRT Japan is now available at cubeSolutions!
As of July 2017, CRScube is now a certified vendor to provide WHODrug Cross Reference Tool Japan(WHODrug CRT Japan), for clients with a valid license with the UMC(Uppsala Monitoring Centre) and Ljoken, the maintenance organization of the Lyakuhinmei Data File(IDF). CRT Japan is a tool developed by UMC and Ljoken that helps easy-conversion of IDF codes to WHODrug codes, and vice versa. As IDF codes are generally used to code clinical and drug safety data by companies in Japan for submission to Japanese Pharmaceuticals and Medical Devices Agency(PMDA), This CRT Japan tool helps eliminating repetitive coding task. For more information, please contact us at email@example.com.
We are looking forward to welcoming you at our booth(#1452) at the 'DIA 2017 Annual Meeting'!
June 18th ~ 22th
McCormick Place | 2301 South King Drive | Chicago, IL 60616, USA
The world's largest exhibition for the multidisciplinary event that brings together a global network of life sciences professionals to foster innovation that will lead to the development of safe and effective medical products and therapies, 'DIA 2017 Annual Meeting' is almost upon us(18th~22th June).
CRScube Inc. is one of the exhibitors this year and we have prepared a booth with dedicated personnel who will be presenting our world-best convenient & qualified eClinical Solutions.
You can join us there for a drink and a friendly chat with the 'CRScube Inc.' team. it is the perfect opportunity to get to know each other better and learn more about what we have to offer you. also, please don't miss this chance to get some souvenirs we prepared for you.
Your presence will do us great honor and we are looking forward to seeing you.
2017 CRScube Annual User Meeting was held at 22nd Mar.
On March 22, CRScube held a User meeting with all customers using cubeSAFETY.
at the very beginning, we were worried about our clients are too busy to attend the meeting, but thankfully this annual meeting end up completed successfully.
The most hot issue in this user meeting was a regulation on the safety of drugs revised on October 28, 2016.
Baek Eun-a, Team manager of boryung Pharma gave a speech on how to use cubeSAFETY along with a summary lecture on the above revised regulations, and it was a very good time for everyone in the meeting.
After that we went over the updated featrues in 2016, and we were able to discuss our opinions based on the results of the "User Survey" that we had previously done.
As a solution provider, it was very good chance for us to listen to the customers' opinions. and we will make every effort to reflect these opinions to our solutions, to become a more friendly CRScube.