Announcements Software for the Biotech & Life Sciences Industry
Improve feature adoption and retention by announcing new features and keeping users informed about key events. Tailored for biotech & life sciences companies to address industry-specific challenges.
Challenges in Biotech & Life Sciences
Biotech and life sciences platforms manage research data, clinical trials, laboratory information, and regulatory submissions. Users are highly educated scientists who demand precision and have zero tolerance for tools that slow down their research workflows.
LIMS platform adoption is low because researchers find manual lab notebooks faster for routine tasks
Clinical trial management system complexity delays study startup and enrollment
Regulatory submission platforms have arcane interfaces that require specialized training
Research data management tools are underutilized, risking data integrity and reproducibility
How Produktly Announcements Helps Biotech & Life Sciences
Everyone loves new features! Announcements are a great way to highlight your new updates and keep customers in the loop.
Announce New Features
- Easily announce new features so users stay up to date.
Rich Text Editor
- Embed videos, images, and GIFs to make announcements engaging.
Targeted Delivery
- Show announcements to the right users at the right time.
Use Cases for Biotech & Life Sciences
LIMS adoption for bench scientists
Guide researchers through logging experiments, recording results, and managing samples in the LIMS with workflows that mirror their existing lab notebook process. Demonstrate that digital data capture is faster and more reliable than manual methods.
Clinical trial management onboarding
Walk clinical operations staff through study setup, site activation, patient enrollment workflows, and monitoring visit preparation in the CTMS. Reduce study startup timelines by ensuring teams use the system efficiently from protocol approval.
Regulatory submission platform training
Provide step-by-step guidance for compiling and submitting regulatory dossiers, including document formatting requirements, cross-reference management, and submission validation. Prevent rejection delays caused by formatting errors or missing components.
Key Metrics to Track
LIMS adoption rate among researchers
Clinical trial startup time
Regulatory submission cycle time
Research data capture compliance rate
Frequently Asked Questions
How do you convince scientists to adopt LIMS over lab notebooks?
Scientists adopt tools that make their work faster, not tools that add bureaucratic overhead. Tours must demonstrate that LIMS entry is as fast as notebook writing, with the added benefits of searchability, data integrity, and regulatory compliance. Start with the most repetitive daily task and show time savings.
Can product tours help with FDA 21 CFR Part 11 compliance?
Yes. Guided workflows ensure electronic records include all required metadata (timestamps, electronic signatures, audit trails). Tours can enforce the correct sequence for data entry, review, and approval that Part 11 requires, reducing the risk of compliance findings during FDA inspections.
How do biotech companies handle onboarding for complex research platforms?
Break the platform into role-specific workflows. A bench scientist needs different tours than a clinical operations manager. Start with the daily bread-and-butter tasks, then progressively introduce advanced analytics and reporting features. Scientists respect tools that respect their time.
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Changelogs
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