PharmaPendium

PharmaPendium

Elsevier
eProtocol

eProtocol

Key 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.

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.

Platforms Supported

Windows Not Supported
Mac Not Supported
Linux Not Supported
Cloud Supported
On-Premises Not Supported
iPhone Not Supported
iPad Not Supported
Android Not Supported
Chromebook Not Supported

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

Audience

Pharmaceutical researchers and regulatory professionals interested in a tool to manage their drug approval data to inform development strategies and ensure compliance

Audience

Research compliance offices, IRB/IACUC committees, investigators, vivarium teams and research administrators at universities, research institutions, hospitals, biotech, pharma and federal agencies.

Support

Phone Support Supported
24/7 Live Support Not Supported
Online Supported

Support

Phone Support Not Supported
24/7 Live Support Not Supported
Online Not Supported

API

Offers API Not Supported

API

Offers API Not Supported

Screenshots and Videos

Screenshots and Videos

No images available

Pricing

No information available.
Free Version Not Supported
Free Trial Not Supported

Pricing

No information available.
Free Version Not Supported
Free Trial Not Supported

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

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Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Training

Documentation Supported
Webinars Not Supported
Live Online Supported
In Person Supported

Training

Documentation Not Supported
Webinars Not Supported
Live Online Not Supported
In Person Not Supported

Company Information

Elsevier
Founded: 1880
Netherlands
www.elsevier.com/products/pharmapendium

Company Information

Key Solutions
Founded: 1991
United States
www.keyusa.com

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Categories

Pharmacovigilance Supported

Categories

Integrations

No info available.

Integrations

No info available.
Claim PharmaPendium and update features and information
Claim PharmaPendium and update features and information
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Claim eProtocol and update features and information