Activate your scientific communication platform with

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:

• 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.

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.

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:

• 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.