The recent past has observed a rise in awareness regarding Pharmacovigilance among stakeholders as a result of which there is a significant increase in data volumes and data complexity. Despite growing awareness, underreporting is widely recognized as a major limitation. Nevertheless, Windward is the sure-shot solution to all PV documentation and reporting needs.
What started as a pilot project in the early 1960s due to Thalidomide disaster now has more than 130 member countries participating in Pharmacovigilance. Pharmacovigilance, the process of detecting, assessing, understanding, and preventing adverse outcomes from drug therapies, has seen significant growth in recent years. According to a report by Global Market Insights, the PV market is predicted to exceed USD8 billion by the year 2024.
With regulatory bodies urging doctors to report more incidences and patients sharing their adverse event stories on different social media channels, there has been a steady rise in the number of PV cases registered. Moreover, regulatory requirements by Health Authority (HA) states that pharma companies need to consider the AE data from multiple data sources – chatbots, public forums, social media, and other channels. With due diligence to this requirement, there has been extensive growth in the number of data channels. Thus, working with tons of data poses a great challenge to PV industries.
Estimates put that large pharmaceutical industries receive around 300,000 to 500,000 Adverse Events per year. With a spectrum of adverse event data and the need to analyze it, the PV processes have turned complex. Amidst this data surge, segregating the AE cases from false alarms, designing documents, and generating reports consume a lot of time and human resources. PV experts relying on programmers, who lack the understanding in developing PV data-powered documents, end up landing into troubles.
This is why Pharmacovigilance highly needs a solution to handle the vast clutter of data and document generation efficiently. Thus, Pharmacovigilance adopts next-generation technology by leveraging the benefits of a document automation system.
Windward, a document automation solution, is bringing about a revolution in the document generation process in Pharmacovigilance.
As data is the cornerstone of pharmacovigilance activities, it is crucial to keep a tab on all the data sources.
To beat the ever-expanding data challenge in pharmacovigilance, Windward offers seamless integration with multiple data sources. Thus, it reduces the disruption caused by disparate data sources and results in increased efficiency through automated document generation.
To ensure the data-driven documents to be sent to regulatory authorities are accurate and as per the standard, Windward facilitates PV experts design documents the way they want. It helps them add value to their data by easily incorporating visuals, charts, tables, and more to make document generation more straightforward and faster.
Windward’s document automation capabilities empower PV experts to tailor their documents for a specific niche. This helps them decrease the time and cost spent on segmenting the reports for different audiences. Thus, document and report generation is just a matter of few minutes with Windward.
With Windward’s Document Automation solution, PV experts need not rely on programmers to create documents. With its easy-to-use interface, non-programmers can take ownership of their templates and allow development to stay on task so they are able to meet internal demands and avoid IT bottlenecks.
As integration is the need of the hour in this rapidly growing data challenge, Windward proves to be the best by delivering integration capabilities. PV experts can integrate their existing and new systems with Windward and enhance efficiency.
Let Windward be your partner to address the data challenges of Pharmacovigilance. Download a free, 30-day trial of Windward Designer and learn more about how Windward works.
The recent past has observed a rise in awareness regarding Pharmacovigilance among stakeholders as a result of which there is a significant increase in data volumes and data complexity. Despite growing awareness, underreporting is widely recognized as a major limitation. Nevertheless, Windward is the sure-shot solution to all PV documentation and reporting needs.
What started as a pilot project in the early 1960s due to Thalidomide disaster now has more than 130 member countries participating in Pharmacovigilance. Pharmacovigilance, the process of detecting, assessing, understanding, and preventing adverse outcomes from drug therapies, has seen significant growth in recent years. According to a report by Global Market Insights, the PV market is predicted to exceed USD8 billion by the year 2024.
With regulatory bodies urging doctors to report more incidences and patients sharing their adverse event stories on different social media channels, there has been a steady rise in the number of PV cases registered. Moreover, regulatory requirements by Health Authority (HA) states that pharma companies need to consider the AE data from multiple data sources – chatbots, public forums, social media, and other channels. With due diligence to this requirement, there has been extensive growth in the number of data channels. Thus, working with tons of data poses a great challenge to PV industries.
Estimates put that large pharmaceutical industries receive around 300,000 to 500,000 Adverse Events per year. With a spectrum of adverse event data and the need to analyze it, the PV processes have turned complex. Amidst this data surge, segregating the AE cases from false alarms, designing documents, and generating reports consume a lot of time and human resources. PV experts relying on programmers, who lack the understanding in developing PV data-powered documents, end up landing into troubles.
This is why Pharmacovigilance highly needs a solution to handle the vast clutter of data and document generation efficiently. Thus, Pharmacovigilance adopts next-generation technology by leveraging the benefits of a document automation system.
Windward, a document automation solution, is bringing about a revolution in the document generation process in Pharmacovigilance.
As data is the cornerstone of pharmacovigilance activities, it is crucial to keep a tab on all the data sources.
To beat the ever-expanding data challenge in pharmacovigilance, Windward offers seamless integration with multiple data sources. Thus, it reduces the disruption caused by disparate data sources and results in increased efficiency through automated document generation.
To ensure the data-driven documents to be sent to regulatory authorities are accurate and as per the standard, Windward facilitates PV experts design documents the way they want. It helps them add value to their data by easily incorporating visuals, charts, tables, and more to make document generation more straightforward and faster.
Windward’s document automation capabilities empower PV experts to tailor their documents for a specific niche. This helps them decrease the time and cost spent on segmenting the reports for different audiences. Thus, document and report generation is just a matter of few minutes with Windward.
With Windward’s Document Automation solution, PV experts need not rely on programmers to create documents. With its easy-to-use interface, non-programmers can take ownership of their templates and allow development to stay on task so they are able to meet internal demands and avoid IT bottlenecks.
As integration is the need of the hour in this rapidly growing data challenge, Windward proves to be the best by delivering integration capabilities. PV experts can integrate their existing and new systems with Windward and enhance efficiency.
Let Windward be your partner to address the data challenges of Pharmacovigilance. Download a free, 30-day trial of Windward Designer and learn more about how Windward works.
The recent past has observed a rise in awareness regarding Pharmacovigilance among stakeholders as a result of which there is a significant increase in data volumes and data complexity. Despite growing awareness, underreporting is widely recognized as a major limitation. Nevertheless, Windward is the sure-shot solution to all PV documentation and reporting needs.
What started as a pilot project in the early 1960s due to Thalidomide disaster now has more than 130 member countries participating in Pharmacovigilance. Pharmacovigilance, the process of detecting, assessing, understanding, and preventing adverse outcomes from drug therapies, has seen significant growth in recent years. According to a report by Global Market Insights, the PV market is predicted to exceed USD8 billion by the year 2024.
With regulatory bodies urging doctors to report more incidences and patients sharing their adverse event stories on different social media channels, there has been a steady rise in the number of PV cases registered. Moreover, regulatory requirements by Health Authority (HA) states that pharma companies need to consider the AE data from multiple data sources – chatbots, public forums, social media, and other channels. With due diligence to this requirement, there has been extensive growth in the number of data channels. Thus, working with tons of data poses a great challenge to PV industries.
Estimates put that large pharmaceutical industries receive around 300,000 to 500,000 Adverse Events per year. With a spectrum of adverse event data and the need to analyze it, the PV processes have turned complex. Amidst this data surge, segregating the AE cases from false alarms, designing documents, and generating reports consume a lot of time and human resources. PV experts relying on programmers, who lack the understanding in developing PV data-powered documents, end up landing into troubles.
This is why Pharmacovigilance highly needs a solution to handle the vast clutter of data and document generation efficiently. Thus, Pharmacovigilance adopts next-generation technology by leveraging the benefits of a document automation system.
Windward, a document automation solution, is bringing about a revolution in the document generation process in Pharmacovigilance.
As data is the cornerstone of pharmacovigilance activities, it is crucial to keep a tab on all the data sources.
To beat the ever-expanding data challenge in pharmacovigilance, Windward offers seamless integration with multiple data sources. Thus, it reduces the disruption caused by disparate data sources and results in increased efficiency through automated document generation.
To ensure the data-driven documents to be sent to regulatory authorities are accurate and as per the standard, Windward facilitates PV experts design documents the way they want. It helps them add value to their data by easily incorporating visuals, charts, tables, and more to make document generation more straightforward and faster.
Windward’s document automation capabilities empower PV experts to tailor their documents for a specific niche. This helps them decrease the time and cost spent on segmenting the reports for different audiences. Thus, document and report generation is just a matter of few minutes with Windward.
With Windward’s Document Automation solution, PV experts need not rely on programmers to create documents. With its easy-to-use interface, non-programmers can take ownership of their templates and allow development to stay on task so they are able to meet internal demands and avoid IT bottlenecks.
As integration is the need of the hour in this rapidly growing data challenge, Windward proves to be the best by delivering integration capabilities. PV experts can integrate their existing and new systems with Windward and enhance efficiency.
Let Windward be your partner to address the data challenges of Pharmacovigilance. Download a free, 30-day trial of Windward Designer and learn more about how Windward works.
