PharmaPendiumElsevier
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eProtocolKey Solutions
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About
PharmaPendium is a comprehensive resource that provides access to FDA and EMA drug approval documents, including pharmacokinetic, pharmacodynamic, and safety profiles. It offers detailed information on drug-drug interactions, adverse effects, and clinical study outcomes, facilitating informed decision-making in drug development and regulatory submissions. The platform's extensive data supports researchers and healthcare professionals in evaluating drug efficacy and safety, contributing to the advancement of pharmaceutical research and patient care. Find information about previous regulatory submissions and profit from precedents to predict agencies’ requirements. Seamlessly move from table view to interactive charts, graphs, and visual aids to easily interrogate and interpret data. Find information by adverse events (MedDRA), targets, indications, drug,s and endpoints using normalized data. Result pages bridge the preclinical to clinical divide.
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About
eProtocol is a web-based research compliance platform for institutions that manage human-subjects, animal, biosafety, and other regulated research. It supports protocol development and electronic submission, committee review and approval workflows, amendments, renewals, adverse-event reporting, automated routing and reminders, version control, meeting agendas and minutes, audit trails, and reporting. Investigators, coordinators, reviewers, and compliance administrators can track protocol status and access records through a shared system. eProtocol includes modules for IRB, IACUC, IBC, stem-cell, chemical-safety, radiation-safety, controlled-substance, and post-approval monitoring workflows. It is designed for universities, research institutions, hospitals and academic medical centers, biotech and pharmaceutical organizations, and government research agencies.
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Platforms Supported
Windows
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Mac
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Linux
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Cloud
Supported
On-Premises
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iPhone
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iPad
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Android
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Chromebook
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Platforms Supported
Windows
Not Supported
Mac
Not Supported
Linux
Not Supported
Cloud
Supported
On-Premises
Supported
iPhone
Not Supported
iPad
Not Supported
Android
Not Supported
Chromebook
Not Supported
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Audience
Pharmaceutical researchers and regulatory professionals interested in a tool to manage their drug approval data to inform development strategies and ensure compliance
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Audience
Research compliance offices, IRB/IACUC committees, investigators, vivarium teams and research administrators at universities, research institutions, hospitals, biotech, pharma and federal agencies.
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Support
Phone Support
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24/7 Live Support
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Online
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Support
Phone Support
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24/7 Live Support
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Online
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API
Offers API
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API
Offers API
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Screenshots and Videos |
Screenshots and VideosNo images available
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Pricing
No information available.
Free Version
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Free Trial
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Pricing
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Free Version
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Free Trial
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Reviews/
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Training
Documentation
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Webinars
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Live Online
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In Person
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Training
Documentation
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Webinars
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Live Online
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In Person
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Company InformationElsevier
Founded: 1880
Netherlands
www.elsevier.com/products/pharmapendium
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Company InformationKey Solutions
Founded: 1991
United States
www.keyusa.com
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Integrations
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Integrations
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