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Process Director for Life Sciences Logo

Process automation solutions designed for life sciences

DOWNLOAD PRODUCT FACT SHEET

Gain end-to-end visibility.

Conquer compliance gaps.

Speed up approvals.


Process Director for Life Sciences helps automate critical processes so the life sciences industry can:

1. Get life-changing products to market faster.

2. Build great experiences for HCPs and patients.

3. Grow and scale without sacrificing efficiency.

 

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Enjoy the best of both worlds.

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

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.

80% pre-built to 20% configurability

 

Explore pre-built life sciences 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. 

    Features
    • Intelligent routing and approval
    • Real-time integrations of journals and congresses data
    • Automated task escalation

  • 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.

    Features
    • Collaborative document authoring
    • Role-based reviewer assignments​
    • Pre-filtered dashboards, based on user ​
      roles assigned at setup
    • Designed specifically to be configurable​

  • 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.

    Features
    • Configurable debarment check routing
    • Always-on audit tracking
    • Training verification
    • Credential checks

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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

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USE CASE

Medical information requests

Handling medical information requests can be challenging without the right technology. With Process Director, 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.

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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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.

 

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