RPA Consulting Services | Microsoft & UiPath Certified | Sunflower Lab
RPA Consulting Services USA

RPA for Pharma Compliance

Automate Regulatory Reporting, Batch Records, and Clinical Data Workflows. Ensure compliance, eliminate manual errors, and automate FDA/EMA reporting in validated environments.

96%
Client Retention
300+
Projects Delivered
15+
Years Experience
80%
Avg. Time Saved
Certified Partners: UiPath Microsoft Solution Partner RoboCorp
Free Consultation
Get Your FDA Compliance Automation Assessment
Tell us what you want to automate. We'll map out a plan in 30 minutes. ✓ Response within 2 business hours
No commitment required. We respond within 2 business hours.
UiPath Certified Microsoft Partner 96% Retention
You're All Set!
A Sunflower Lab RPA consultant will reach out within 2 business hours.

We'll review your process and come prepared with automation options, timeline, and estimated ROI.
80–90%
Time saved in customer onboarding — Hoganas
1,200 hrs
Annual hours saved on shift data entry — MAI
70%
Reduction in PO processing time — IONM
15%
Admin time cut with patient letter automation

Reduce Risks and Errors in Pharma

Manufacturing — Power Automate
80%
Employee hours saved
Hoganas automated customer onboarding and credit approval workflows. Delivery report creation dropped from 5 hours to under 1 hour. Real-time updates eliminated manual follow-up entirely.
Hoganas
Manufacturing — Power Apps
1,200
Hours saved annually
MAI replaced plant-by-plant spreadsheets with a centralized Power Apps data entry system, eliminating errors and redundant effort across all facilities.
Modular Assembly Innovations
Manufacturing- Power Platform
90%
Increase in Efficiency
Dominion Engineering automated Product Inspection Workflow with Microsoft Power Platform & eliminated need for a person to spend 10-15 hours a week emailing the inspection personnel.
Dominion Engineering

From first call to
live bots in 4–8 weeks.

01
Free Assessment
We audit your workflows in a 30-minute call, identify high-ROI automation candidates, and give you a written recommendation — at no cost.
02
Solution Design
Our team maps the bot logic, exception handling, and integration points. You approve the design before we write a single line of code.
03
Build & Test
We develop, test, and validate the automation in your environment. Most clients see their first bot live within 3–4 weeks.
04
Go Live + Support
We deploy, monitor, and support your bots post-launch. 24/7 managed services available to keep your automation running at peak performance.

End-to-End RPA for Compliance Pharma Use Cases
We handle everything.

🔐
Regulatory Compliance Automation
  • Automate regulatory submissions and documentation workflows
  • Extract and compile data for FDA/EMA reporting
  • Maintain audit-ready records across systems
  • Automate regulatory reporting for pharma compliance teams
  • 📊
    Batch Record Automation
  • Automate batch record data collection and validation
  • Review electronic batch records across systems
  • Flag discrepancies automatically before submission
  • Automate batch record processing for GMP compliance
  • Data Validation Automation
  • Validate clinical and production data across systems
  • Cross-check data against compliance rules
  • Identify inconsistencies in real time
  • Enable clinical data automation with rule-based validation
  • 📈
    FDA / EMA Reporting Workflows
  • Automate report generation for regulatory authorities
  • Consolidate data from multiple systems into submission-ready formats
  • Trigger alerts for compliance gaps
  • Accelerate FDA and EMA reporting workflows with RPA
  • "Repetitive and time-consuming tasks that used to take up a significant portion of the team's workday are now handled seamlessly by the RPA system. Your team's support throughout development and implementation was exceptional."
    GB
    Gene Boucher
    Operations — ZinniaX
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