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What is eProtocol?

eProtocol is an all-encompassing online platform designed for research compliance, catering to various institutions that manage studies involving human subjects, animals, biosafety, and other regulated areas. This system streamlines the creation and electronic submission of research protocols while managing the workflows needed for committee review, approval, amendments, renewals, and reporting of adverse events, along with features like automated routing, reminders, version control, meeting agendas, minutes, audit trails, and detailed reporting. Investigators, coordinators, reviewers, and compliance administrators benefit from a collaborative interface that allows them to effectively track protocol statuses and access essential records. The platform includes specialized modules for Institutional Review Boards (IRB), Institutional Animal Care and Use Committees (IACUC), Institutional Biosafety Committees (IBC), as well as for stem-cell research, chemical safety, radiation safety, controlled substances, and post-approval monitoring. eProtocol is meticulously designed to cater to the specific needs of universities, research institutions, hospitals, academic medical centers, biotech and pharmaceutical firms, and governmental research entities, ensuring an efficient compliance process across a variety of research landscapes. Furthermore, it not only boosts the efficiency of regulatory processes but also plays a crucial role in enhancing the overall integrity and safety of research activities, fostering a culture of accountability and transparency in scientific inquiry.

What is PharmaPendium?

PharmaPendium is a comprehensive resource that provides users with access to a wide range of drug approval documents from the FDA and EMA, covering crucial elements such as pharmacokinetics, pharmacodynamics, and safety assessments. This platform offers valuable insights into drug interactions, adverse effects, and clinical trial outcomes, enabling stakeholders to make informed decisions in both drug development and regulatory submissions. Its extensive database supports researchers and healthcare professionals in evaluating the safety and effectiveness of various medications, thereby playing a critical role in advancing pharmaceutical research and improving patient care. Users can also investigate historical regulatory submissions and utilize previous cases to gain a clearer insight into agency expectations. The user-friendly interface facilitates an easy transition from raw data to engaging visual representations like charts and graphs, enhancing the analysis and interpretation of results. Furthermore, the platform allows users to search for information on adverse events (MedDRA), therapeutic targets, drug indications, and endpoints through standardized data. Result pages effectively link preclinical research with clinical applications, offering a holistic view of the drug development ecosystem. Overall, PharmaPendium not only simplifies the research process but also encourages collaboration and knowledge exchange among professionals in the industry, ultimately contributing to better health outcomes. The array of features offered by this platform makes it an invaluable tool for those involved in the pharmaceutical field.

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Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

Pricing not provided

Supported Platforms

SaaS
On-Prem

Supported Platforms

SaaS

Customer Service / Support

Not specified

Customer Service / Support

Standard Support
Web-Based Support

Training Options

Not specified

Training Options

Documentation Hub
Online Training
On-Site Training

Company Facts

Organization Name

Key Solutions

Date Founded

1991

Company Location

United States

Company Website

www.keyusa.com

Company Facts

Organization Name

Elsevier

Date Founded

1880

Company Location

Netherlands

Company Website

www.elsevier.com/products/pharmapendium

Categories and Features

Research Management

Not specified

Categories and Features

Pharmacovigilance

Not specified

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