Features
Key Features
Digital Documentation
Go paperless with digiEC's advanced document management system, ensuring secure access, review, and approval of crucial documents.
Online EC Submission and Approval
Researchers can submit proposals online, and committee members can review and approve submissions within the user-friendly digiEC platform, reducing processing times.
Document Management
Ensure data integrity and compliance. With digiEC, securely store and organize documents, meeting archival requirements for regulatory compliance.
Finance Management
Take control of your budget. digiEC includes finance management tools to track and manage project budgets, providing transparency and accuracy in financial oversight.
Security and Compliance
Your data, our priority. digiEC is built with the highest standards of security and compliance, safeguarding sensitive information and aligning with industry regulations.
SOP Management
Enforce consistency in procedures. digiEC centralizes Standard Operating Procedures (SoPs), making it easy to manage and adhere to established protocols.
Audit Ready
Be prepared for audits at all times. digiEC's robust features and secure infrastructure guarantee that your committee is audit-ready, providing confidence in the face of regulatory scrutiny.
ICH GCP and NDCT Compliant
Align with global standards. digiEC complies with ICH GCP and New Drugs and Clinical Trials Rules (NDCT) standards. Data based on ICMR Guidelines
Free Good Clinical Practice Training
Access free GCP training through digiEC, ensuring that your committee members are up-to-date with the latest regulatory requirements and ethical standards.
About digiEC
What’s Unique?
The reason around half of all clinical trials are conducted on paper is that until now there has been no really viable alternative for the smaller to mid-sized trial. Existing systems are complex, slow to set up and expensive. DigiEC is a system built from the ground up with the sole purpose of providing a system that’s quick to set up, simple to use and allows flexible, mobile access. Fundamental to the design was to provide all the key functionality you are likely to need; the ability to interrogate and report you require; and offer the security and compliance you know is a necessity… in a package that makes it all cost-effective.
In DigiEC, we believe we have succeeded in creating a complete solution that’s accessible to all, and that
gives trial managers greater control of their trials.
Elevate your clinical research ethics committee's capabilities with digiEC.
Registration/Re-registration Services
EC Management Consulting
EC Coordinator/ Staffing Solutions
EC Trainings on ICH-GCP, ICMR Guidelines,
etc.
Key Features
- Streamline your submission and review processes
- Reduce paper, packets and mailings
- Cut time wasted on redundant and clerical work.
- Reduce administrative tasks to allow staff to focus on complex issues and support your research community.
- Facilitate clear, coordinated communications and track correspondence.
- Enable Members, Researchers and Administrators to access data anytime, anywhere.
- Manage your meetings and committees.
- Increase process transparency.
- Increase data security.
- Maintain a clear audit trail with appropriate documentation and versioning.
- Increase control and reinforce guidance and consistency throughout the process.
- Share information seamlessly and securely in real time, wherever your research community may be.
- Improve the quality of documentation and study design.
- Security and Compliance
- Independently assessed against GXP & FDA 21 CFR 11 standards every year.
- Member of the Clinical Data Interchange Standards consortium (CDISC)
- Latest encryption technologies
- Secure servers
- User-Friendly Interface, Platform Independent
- No installation is required, All you need is a browser.
Contact
Contact Us
Our Address
38, Laghuvetan Society, Near Kachore Lawn, Somalwada Road, Manish Nagar, Nagpur Pincode: 440015 (Maharashtra)
Email Us
info@digiec.in
Call Us
+91 94048 26895