contact@easycr.com.my

Ready to propel your clinical trials with Easy Clinical Research (ECR)

Easy Clinical Research (ECR) provides solutions that include software and services that allow clients/ sponsors to achieve clinical results by streamlining the capture and management of clinical study data.

Clinical Data Management (CDM) is a critical phase in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. The vehicle to support CDM process is a reliable eCRF platform.

Who we are

We have a dedicated consultants and technical support personnel to ensure our commitment to provide quality services to our clients. In addition, we partner with a number of other trusted and qualified companies to support comprehensive service needs of our clients. Our collaboration with our alliances creates dynamic partnerships to serve our clients better by keeping the costs low and relieve of the burdens and overheads of our clients so that they can focus on other aspects of their research.


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How to Apply

How to Apply for a ECR Account ?. You must have a ECR account to register study information. ECR establishes one account for a study. All investigators from that study (who are conducting studies) are typically designated as users of this single ECR account (own user ID). The Study should designate one or more ECR Administrators to manage the account and to create logins for additional users. If an administrator is not designated, ECR may assist in identifying appropriate individuals to act as ECR Administrators for a study. All ECR accounts should have at least one administrator.

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Support

Objective of this platform: is to set up a user-friendly database infrastructure which amalgamates the clinical research needs of the individual / groups of investigator initiated research / study. By utilizing Web-based technology, open source system and the mid-range level of data security will be leveraged to support the research team with access to data that can support current and future clinical research endeavours.




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DATA SECURITY

All information will be stored in linked data tables. Identifying information (name and email address) will be stored in separate (but linked) data tables.

Data transmission: ECR currently utilizes 128‐bit secure socket layer (SSL) protocol which protects all data transmission sent over the internet between the web server and every client machine.

Secure servers: All data is housed on a secure server.

Antivirus software: All servers are protected from viruses using anti‐virus software. This software automatically checks for virus signature file updates once an hour, and if necessary, directly updates itself. All antivirus software is monitored and network personnel notified in the event that the software stops functioning on a server.

Firewall: The network, including all the servers that will store our research data, is behind a secure firewall that does not allow unauthorized access to any research data server.

Disaster recovery: The registry database is backed up regularly to ensure that no data is lost. Our disaster recovery system also follows Standard Operating Procedures to maintain full security of backup data.

Cloud services: In addition to use of our secure servers, we may use your data in conjunction with cloud storage and computing services in order to assist with communication, data collection, storage, and processing. Third‐party vendors will be vetted for their security practices and will meet or exceed privacy and security standards for electronic research health records management.

Pricing

Our pricing is based on the type of sponsor and the number of studies.

Demo Account

Just get familiarize with our system

  • Register
  • Login
  • ECR Screens
  • View Report Formats
RM 0.00
Regsiter

Individual

For research scholors with academic sponsors

  • 1 Study at a time
  • 1 Principal Investigator
  • 1 Researcher
  • Duration: 6 Months
RM 5,000.00
Regsiter

Company

For Companies and Organisations

  • Multiple Studies
  • Multiple Principal Investigators
  • Multiple Researchers
  • Duration: 6 Months
Please
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Get Started

If you have checked out our demo and now want to get started using the Easy Clinical Research (ECR) for your trial / Research, just follow these steps:

1. If this is the first time you are using the Easy Clinical Research (ECR) for a trial / Research, please register your details in ECR. Once you've registered on our production system, you can start exploring the demo version or proceed to the payment gateway to set up your study

2. Once demo duration is expired, you may request for extension from the admin for an extension (for a limited time only)

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