Atlant Systems Incorporated
Atlant Systems, Inc. is a leader in providing software business solutions primarily to the pharmaceutical, biopharmaceutical, and medical device industries worldwide. They develop and deploy systems and procedures that meet the needs of growing biotech companies, helping them conduct clinical trials, track product safety, manage regulatory documents, and more. Their mission is to offer high-quality, technologically advanced, and configurable solutions to accelerate clinical research, management of clinical trials, and regulatory oversight.
Industries
Nr. of Employees
small (1-50)
Atlant Systems Incorporated
Wilmington, Massachusetts, United States, North America
Products
Two-factor authentication and single sign-on solution
Secure access solution providing strong two-factor authentication and single sign-on for server access and collaborative systems.
Electronic Document Management System (EDMS)
Document management system tailored for enterprise and departmental electronic document capture, authoring, distribution, retrieval, and global management.
Adverse event reporting system
Tool for generating and managing adverse event reports from clinical sites to support clinical safety and reporting workflows.
Configurable Clinical Trials Management System (CTMS)
Full-scope, configurable off-the-shelf clinical trials management system for managing global trials, sites, investigators, enrollment, regulatory documents, monitoring, and budget tracking.
Two-factor authentication and single sign-on solution
Secure access solution providing strong two-factor authentication and single sign-on for server access and collaborative systems.
Electronic Document Management System (EDMS)
Document management system tailored for enterprise and departmental electronic document capture, authoring, distribution, retrieval, and global management.
Adverse event reporting system
Tool for generating and managing adverse event reports from clinical sites to support clinical safety and reporting workflows.
Configurable Clinical Trials Management System (CTMS)
Full-scope, configurable off-the-shelf clinical trials management system for managing global trials, sites, investigators, enrollment, regulatory documents, monitoring, and budget tracking.
Services
Two-week consulting engagement to evaluate business needs, document requirements, perform gap analysis, prioritize requirements, and deliver an SRS, deployment plan, budget, and ROI estimate for CTMS implementation.
Assessment and redesign of clinical workflows to align processes with collaborative trial management systems and improve operational efficiency.
Services to bring systems and procedures into alignment with regulatory requirements such as electronic records, privacy, and financial controls.
Online system to track and manage product issues reported by users.
Provision of an evaluation and selection process and whitepaper to guide organizations in selecting scalable CTMS solutions appropriate to their operational model.
Two-week consulting engagement to evaluate business needs, document requirements, perform gap analysis, prioritize requirements, and deliver an SRS, deployment plan, budget, and ROI estimate for CTMS implementation.
Assessment and redesign of clinical workflows to align processes with collaborative trial management systems and improve operational efficiency.
Services to bring systems and procedures into alignment with regulatory requirements such as electronic records, privacy, and financial controls.
Online system to track and manage product issues reported by users.
Provision of an evaluation and selection process and whitepaper to guide organizations in selecting scalable CTMS solutions appropriate to their operational model.
Expertise Areas
- Clinical trial management
- Clinical process re-engineering
- Regulatory compliance consulting
- Electronic document management
Key Technologies
- Clinical Trial Management Systems (CTMS)
- Electronic Document Management Systems (EDMS)
- Cloud-based CRM and cloud platforms
- Two-factor authentication and single sign-on
News & Updates
The global clinical trial management system (CTMS) market is expected to grow 14% over a five-year period hitting an almost $2bn valuation by 2019, according to a new market report.
Protocol Manager - Planning has passed the Security Review process and now available in Appexchange - an online application marketplace by Salesforce. It helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.
adWATCH – AE helps pharmaceutical organizations manage and report adverse events that occur during clinical trials. It provides a fast and effective means of generating and managing Adverse Event Reports (AERs).
MedDRA is a clinically validated international medical terminology dictionary used by regulatory authorities in the pharmaceutical industry during the regulatory process and for data entry, retrieval, evaluation, and presentation. It is now available as a cloud solution in Appexchange.
The global clinical trial management system (CTMS) market is expected to grow 14% over a five-year period hitting an almost $2bn valuation by 2019, according to a new market report.
Protocol Manager - Planning has passed the Security Review process and now available in Appexchange - an online application marketplace by Salesforce. It helps clinical operations manage global trials of drugs, devices, biologics, and vaccines in all phases of development.
adWATCH – AE helps pharmaceutical organizations manage and report adverse events that occur during clinical trials. It provides a fast and effective means of generating and managing Adverse Event Reports (AERs).
MedDRA is a clinically validated international medical terminology dictionary used by regulatory authorities in the pharmaceutical industry during the regulatory process and for data entry, retrieval, evaluation, and presentation. It is now available as a cloud solution in Appexchange.