Our powerful medical affairs software accelerates approval workflows and simplifies compliance so you can stay ahead in the life sciences market.
In the ever-changing world of life sciences, medical affairs teams can't afford to fall behind.
Outdated publication management tools and processes can result in delayed approvals, compliance headaches, and missed opportunities that jeopardize market success.
Publication planning and management is only one piece of a time-consuming drug approval process, but as we saw during the pandemic, the ability to move swiftly is a significant competitive advantage for pharmaceutical companies.
PubPro helps increase the agility and speed of your approval process so you can get to market faster without compromising the integrity or safety of your products.
Many publication management tools require medical affairs teams to adapt their unique, proprietary processes to fit the rigid confines of one-size-fits-all technology.
In an effort to adhere to their organization's SOPs, users eventually find themselves performing 30%+ of the process outside of the system. Forcing users to adopt clunky workarounds and switch between multiple applications reduces productivity and process visibility.
PubPro is configured to your unique SOPs, which means you can ensure every step in the process is conducted in a single application.
As the development of pharmaceutical products becomes more specialized and unique, the necessity for rigorous scientific integrity and meticulous regulatory oversight has never been more critical.
There is no room for errors or hiccups when potentially life-saving therapies are on the line.
PubPro helps medical affairs teams ensure their publication management processes are air-tight and constantly adapting to ever-changing regulatory and business requirements.
Other competitors |
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PubPro |
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External users must log in to review | Email deep linking allows external users to review without logging in | |
Leaders must manually update assignments for each publication and after team changes | Automated, role-based reviewer assignments | |
Credential checks manually performed by other departments | Automated, configurable routing of credential check results | |
Complicated dashboards that users must configure themselves | Pre-filtered dashboards, based on user roles assigned at setup | |
Hard or expensive to customize | Designed specifically to be configurable |
|
|
PubPro |
---|---|---|
External users must log in to review | Email deep linking allows external users to review without logging in | |
Leaders must manually update assignments for each publication and after team changes | Automated, role-based reviewer assignments | |
Credential checks manually performed by other departments | Automated, configurable routing of credential check results | |
Complicated dashboards that users must configure themselves | Pre-filtered dashboards, based on user roles assigned at setup | |
Hard or expensive to customize | Designed specifically to be configurable | |
Journals and congresses data obtained separately | Real-time integrations of journals and congresses data |
|
|
PubPro |
---|---|---|
External users must log in to review | Email deep linking allows external users to review without logging in | |
Leaders must manually update assignments for each publication and after team changes | Automated, role-based reviewer assignments | |
Credential checks manually performed by other departments | Automated, configurable routing of credential check results | |
Complicated dashboards that users must configure themselves | Pre-filtered dashboards, based on user roles assigned at setup | |
Hard or expensive to customize | Designed specifically to be configurable | |
Journals and congresses data obtained separately | Real-time integrations of journals and congresses data |
This question is at the heart of Esperion Therapeutics' decision to replace their existing publication software with PubPro.
In this customer story, read about Esperion Therapeutics' journey to a more efficient and effective publication management process.
As the life sciences industry evolves, medical affairs teams are left wondering why software solutions haven't kept pace with their needs. Teams often must choose between expensive, complex systems or inefficient, piecemeal solutions.
In our downloadable guide, we will show you how to identify "happy medium" software solutions that offer robust functionality while remaining user-friendly and adaptable to specific organizational needs.
Extend the functionality of PubPro with modules designed for strategic publication planning and journals and congresses data.
Create and maintain a strategic publication roadmap with PubPro’s Publication Planning Dashboard.
Amplify the influence of your scientific publications so you can drive adoption with providers and patients and secure reimbursement from payers.
Get publications to the right place at the right time with our Journals & Congresses Portal.
Access a vast, curated selection of medical research journals and scientific congress listings to find the most relevant match for your publication.
(Don't need a full publication management solution? PubPro's journals and congresses data is also available to purchase separately. Contact us to learn more.)
Our flexible, scalable process automation solutions empower medical affairs teams at life science organizations to operate better and do their best possible work.
With Process Director, you get a process engine that works every time.
There's endless possibilities for automating and optimizing other processes, whether you use one of our pre-built use cases or create your own.
Enjoy the greatest bang for your buck as you create more new processes.
Get the convenience of SaaS with the added luxury of a consultative business partnership. We’re there to support you every step of the way.
Get the speed and affordability you need, plus powerful customization options not available in competing publication management solutions.
PubPro offers the perfect balance of pre-built functionality and flexibility, with 80% of the solution already built and the remaining 20% configured to your organization's specific requirements.