Transform medical affairs with BP Logix's life sciences automation platform

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Process Director for Life Sciences is a low-code automation platform that helps the life sciences industry:

  • Streamline critical business processes

  • Reduce regulatory compliance risk

  • Enhance operational efficiency with ease

With Process Director for Life Sciences, organizations can innovate faster, achieve greater agility, and accelerate digital transformation.

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Get life-changing products to market faster

Build A+ experiences for providers and patients

Grow and scale without sacrificing efficiency

Enjoy the best of both worlds

Our use cases offer a perfect balance of pre-built functionality and flexibility, with 80% of the solution already built and the remaining 20% configured to your company's specific requirements.

Get the speed and affordability you need, plus powerful customization options not available in competing SaaS solutions.

80% pre-built to 20% configurability

 

Explore our pre-built use cases:

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USE CASE

Publication management

Get new drugs and therapies to market, faster. PubPro helps medical affairs teams cut life sciences publication costs by up to 50% and reduce submission times from hours to minutes. 

Product fact sheet: DOWNLOAD PDF
  • Speed up time-to-market.

    Publication planning and management is only one piece of a time-consuming drug approval process. The ability to move swiftly is a significant competitive advantage for life sciences companies.

    PubPro increases the agility and speed of critical publication workflows so you can get to market faster without compromising the integrity or safety of your products. 

  • Automate according to your unique SOPs.

    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.

    PubPro is configured to your unique SOPs, which prevents your users from adopting clunky workarounds or switching between multiple applications.

  • Reduce errors and compliance risks.

    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.

 

 

"With the ability to have multiple reviewers working on the same document simultaneously, our medical affairs team will be able to save so much time."

— Cecilia Petrella
Director of Medical Affairs at LimFlow

Level up your publications

Extend the functionality of PubPro with powerful modules for strategic publication planning and journals and congresses data.

DASHBOARD MODULE

Publication Planning

Create and maintain a strategic publication roadmap that amplifies the influence of your scientific publications and drives greater adoption by payers, providers, and patients.

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DATA PORTAL

Journals and Congresses

Submit publications to the right place at the right time with access to our vast, curated selection of medical research journals and scientific congress listings.

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Other competitors

 
 

PubPro

Leaders must manually update assignments for each publication and after team changes Automated, role-based reviewer assignments
Debarment checks manually performed by medical affairs and legals department Configurable routing of debarment 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


Other competitors

 
 

PubPro

Leaders must manually update assignments for each publication and after team changes Automated, role-based reviewer assignments
Debarment checks manually performed by medical affairs and legals department Configurable routing of debarment 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


Other competitors

 
 

PubPro

Leaders must manually update assignments for each publication and after team changes Automated, role-based reviewer assignments
Debarment checks manually performed by medical affairs and legals department Configurable routing of debarment 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

 

USE CASE

Regulatory document management

Approvia centralizes cross-departmental document management, ensuring critical regulatory affairs submission processes for INDs and NDAs remain on track.

  • Bundle regulatory documents into dossiers.

    Approvia groups documents, reviewers, and processes into dossiers and then automatically assigns tasks to users based on their pre-configured role in the process.
  • Loop in external reviewers with one click.

    Approvia’s collaborative document editor allows submitters and reviewers to work together in real-time. Need to loop in an external reviewer? Deep linking notifications makes it easy for these users to securely access and contribute to documents with one click — no login required.

  • Reduce errors and compliance risks.

    Regulatory submission processes require coordination across different departments. Without a universal source of truth, companies risk costly delays and rejections. Approvia's granular audit logs ensure your application and regulatory submission documents follow FDA guidelines, eliminating the risk of delays or rejection.

Without Approvia:

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With Approvia:

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USE CASE

Medical information requests

Handling medical information requests can be challenging without the right technology. With MIRador, you can centralize MIRs from internal and external stakeholders, including adverse event recordings to HCP dosage questions.

Product fact sheet: DOWNLOAD PDF
  • Respond quickly to MIRs.

    How long does it take for HCPs and patients to receive a response to their medical information request?

    Our solution improves the user experience of HCPs and patients by helping you process MIRs faster.

  • Speed up report generation.

    Struggling with tedious, time-consuming report generation due to decentralization of information across multiple data sources?

    Compile data from multiple systems and sources so you can quickly generate weekly, quarterly, and yearly reports. 

  • Optimize with predictive analytics.

    Assuring compliance with regulatory guidance and company-specific policies doesn't need to be an overly complex process.

    Our platform's valuable performance insights make it easy to identify bottlenecks, assure compliance, and continuously improve processes. 

Why BP Logix?

Our flexible, scalable process automation solutions empower medical affairs teams at life science organizations to operate better and do their best possible work.

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Built on a powerful low-code platform

With Process Director, you get a process engine that works every time.

 

Easily scale to support new processes

There's endless possibilities for automating and optimizing other processes, whether you use one of our pre-built use cases or create your own.

Cost-effective platform licensing

Enjoy the greatest bang for your buck as you create more new processes.

 

We're more than a SaaS provider

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.

One-size-fits-all technology doesn't work for medical affairs.

Book a call today to learn more about BP Logix's purpose-built life science automation solutions.

Life sciences reads & resources

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WHITE PAPER

How are you adapting to the changing role of medical affairs?

It’s no secret that life science organizations must adapt and harness new technologies in order to stay competitive in the market and comply with regulations. Read more in our exclusive white paper.

Download: The Evolving Role of Medical Affairs

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