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Description

By fostering robust partnerships with top Contract Research Organizations (CROs), we provide an innovative approach to the secure onboarding and evaluation of research studies. Our exceptional user experience in study management and image analysis, combined with integrated artificial intelligence, greatly enhances the productivity of our pathologists. The cutting-edge cloud-based system facilitates immediate collaboration between pharmaceutical companies and CRO partners globally, regardless of location. Users maintain comprehensive control over the configuration of their studies, accommodating various types of associated data, study sizes, and formats from Whole Slide Imaging (WSI) vendors, including capabilities for SEND data representation and LIMS integration, all presented through an easy-to-navigate interface. We combine efficient workflow design, outstanding viewing performance, and user-friendliness to create a distinctly superior digital pathology experience. Patholytix Preclinical stands as a fully scalable solution that adapts to the evolving needs of your organization, ensuring seamless access to studies whether in the office or working remotely. This adaptability not only enhances operational efficiency but also empowers teams to collaborate more effectively in a rapidly changing research landscape.

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 No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

No details available.

Integrations

No details available.

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) Yes 
Online Support Yes 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) Yes 
In Person Yes 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) Yes 
In Person Yes 

Vendor Details

Company Name

Patholytix

Country

Ireland

Website

www.patholytix.com

Vendor Details

Company Name

Elsevier

Founded

1880

Country

Netherlands

Website

www.elsevier.com/products/pharmapendium

Product Features

Product Features

Alternatives

Alternatives

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