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Description
Enhance your biomedical research endeavors through the most extensive database of biomedical literature available globally. By utilizing a thorough and contemporary search process, you can access a wealth of biomedical evidence that is both comprehensive and pertinent. Streamline your systematic searches with automated query generation facilitated by user-friendly search forms. Discover critical insights into drug-disease interactions and drug-drug relationships, meticulously curated through extensive indexing efforts. The rapid evolution of biomedical research and development necessitates access to exhaustive information, allowing you to identify potential risks by evaluating all known data. Furthermore, you can monitor safety standards to ensure compliance with regulations while unveiling connections that foster innovation. Embase stands out as a distinctive medical literature database where depth of content exceeds mere quantity. With Emtree indexing of full-text resources and specialized search terminology, you are empowered to locate all significant and up-to-date information, including data that may elude other databases. Scroll down to understand the compelling reasons why regulatory bodies endorse Embase within their best practice recommendations, ensuring that your research is not only thorough but also aligned with industry standards. This commitment to excellence in biomedical literature further positions Embase as an indispensable tool for researchers and practitioners alike.
Description
PharmaPendium serves as a robust platform that grants users access to a wide array of FDA and EMA drug approval documents, encompassing essential aspects like pharmacokinetics, pharmacodynamics, and safety evaluations. This resource delivers in-depth insights into drug-drug interactions, side effects, and outcomes from clinical studies, thereby empowering stakeholders to make well-informed decisions during the drug development process and when making regulatory submissions. Its rich database aids researchers and healthcare practitioners in assessing both the efficacy and safety of medications, playing a pivotal role in the progression of pharmaceutical research and enhancing patient care. Users can explore historical regulatory submissions and leverage past precedents to better understand and anticipate agency requirements. The interface allows for a seamless transition from tabular data to dynamic charts, graphs, and other visual tools, making it easier to analyze and interpret findings. Additionally, users can search for information related to adverse events (MedDRA), therapeutic targets, drug indications, and endpoints utilizing standardized data. Result pages effectively connect preclinical research with clinical applications, facilitating a comprehensive understanding of the drug development landscape. Overall, this platform not only streamlines the research process but also fosters collaboration and knowledge-sharing among industry professionals.
API Access
Has API
API Access
Has API
Integrations
CoVigilAI
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Elsevier
Country
Netherlands
Website
www.embase.com/landing
Vendor Details
Company Name
Elsevier
Founded
1880
Country
Netherlands
Website
www.elsevier.com/products/pharmapendium