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What is adWATCH?

adWATCH - AE serves as a comprehensive solution for pharmaceutical companies to effectively manage and document adverse events that may occur throughout clinical trials. It offers a rapid and streamlined method for individuals at clinics, hospitals, or research sites to generate and monitor Adverse Event Reports (AERs), ensuring that all necessary information is accurately relayed to regulatory authorities and governmental entities. An adverse event is defined as any harmful or negative reaction a patient experiences as a result of medications or medical devices. The meticulous documentation of these adverse events requires detailed tracking of all medical case specifics, which leads to the production of essential reports such as MedWatch and CIOMS. With the implementation of adWATCH - AE, researchers, physician investigators, Contract Research Organizations (CROs), and various healthcare professionals can efficiently create and submit AERs that comply with FDA standards, following the formats established by both MedWatch and CIOMS. This organized approach not only bolsters adherence to regulatory guidelines but also significantly enhances the oversight of patient safety during the course of clinical trials. Furthermore, the tool's user-friendly interface facilitates collaboration among multiple stakeholders, contributing to a more transparent and accountable research environment.

What is DrugPatentWatch?

In the global biopharmaceutical industry, business intelligence centers around understanding the evolving dynamics of drug patents and the emergence of generic medications. Accurately predicting future financial requirements and actively identifying generic substitutes are crucial for sustained success. By examining the successes of former patent challengers, companies can gain valuable insights into the competitive environment and shape their research trajectories. This kind of analysis is essential for informing portfolio management strategies for upcoming drug development initiatives. Moreover, effectively anticipating when patents for branded medications will expire, identifying likely generic suppliers, and managing the inventory of branded drugs are critical tasks. In addition, obtaining comprehensive data on formulation and manufacturing enables the identification of pivotal formulators, repackagers, and relabelers, which can optimize operations and improve market positioning. Grasping these factors is vital, as it can lead to enhanced strategic decision-making, ultimately driving the biopharmaceutical sector toward innovation and growth. By leveraging this intelligence, companies can better navigate the complexities of the market to stay ahead of the competition.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

$250 per month
Free Version

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Web-Based Support

Customer Service / Support

Web-Based Support

Training Options

Documentation Hub
Online Training

Training Options

Not specified

Company Facts

Organization Name

Atlant Systems

Company Website

atlantsystems.com/atlant/solutions/atwatch-ae/

Company Facts

Organization Name

DrugPatentWatch

Date Founded

2003

Company Location

United States

Company Website

www.drugpatentwatch.com

Categories and Features

CAPA

Not specified

Drug Discovery

Not specified

Categories and Features

Drug Discovery

Not specified

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