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Limited Time Offer: Full Feature Access. Plans start @$13 for 11 users Get Started Now
Streamline your R&D processes with Orangescrum’s comprehensive project management tools. Track research progress, manage experiments, and collaborate seamlessly with cross-functional teams to accelerate drug discovery and development. Use custom templates and workflows to standardize processes, ensuring consistency and reducing errors.
Ensure adherence to stringent regulatory requirements with Orangescrum’s compliance tracking features. Maintain accurate records, manage documentation, and generate reports to demonstrate compliance with industry standards and regulations. Automate the management of compliance tasks and deadlines to avoid regulatory penalties and ensure timely submissions to authorities like the FDA and EMA.
Efficiently manage clinical trials from planning to execution. Use Orangescrum to schedule trials, monitor participant progress, manage data collection, and ensure compliance with regulatory protocols. Track patient recruitment, manage informed consent documents, and oversee trial sites with integrated communication tools. Ensure data integrity and streamline reporting to regulatory bodies.
Maintain high standards of quality with Orangescrum’s QA/QC management tools. Track quality control processes, manage inspections, and ensure that all pharmaceutical products meet the required specifications and safety standards. Implement corrective and preventive actions (CAPA) and monitor their effectiveness. Automate quality audits and manage compliance with GMP (Good Manufacturing Practices).
25% Improvement in R&D Efficiency
Top Pharmaceuticals optimized resource allocation, enhanced collaboration, and automated routine tasks, the company saw a 25% improvement in R&D efficiency.
35% Increase in Compliance Accuracy
A Large pharma utilized comprehensive compliance tracking and automated documentation management, to achieve a 35% increase in compliance accuracy.
40+ Hours Saved Per Week in Clinical Trial Management
Global Pharma saved over 40 hours per week in managing clinical trials by leveraging trial management features.
Access Google Drive, Dropbox, Slack, GitHub, Zoom, SSO, Zapier, Google Calendar and OneDrive bringing them all together within Orangescrum.
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Designed to meet your unique project management needs, our templates streamline R&D, clinical trials, and compliance processes.
Gain control over your research and development processes with Orangescrum’s tailored templates. Enhance collaboration, streamline workflows, and track progress to drive successful drug development.
Monitor research activities, track milestones, and manage experiment data to ensure timely progress.
Facilitate communication and coordination among researchers, scientists, and project managers for efficient.
Automate routine tasks and approvals to accelerate R&D processes and reduce manual effort.
Optimize the management of clinical trials with Orangescrum’s dedicated templates. Streamline trial scheduling, participant tracking, and regulatory compliance to enhance trial efficiency and effectiveness.
Plan and manage trial phases, recruit participants, and coordinate with trial sites to ensure smooth execution.
Track participant progress, manage consent forms, and monitor data collection to maintain trial integrity.
Ensure compliance with regulatory requirements by automating documentation and reporting processes.
Ensure adherence to industry regulations and maintain high-quality standards with Orangescrum’s compliance and QA templates. Monitor quality control, manage documentation, and streamline compliance efforts.
Track regulatory requirements, manage compliance documentation, and automate reporting.
Monitor quality assurance processes, conduct inspections, and manage corrective actions to ensure product safety.
Organize and manage critical documentation related to quality and compliance, ensuring accessibility.
You have completed the onboarding process and are now ready to start managing your projects with our application.
