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Company description

Sierra Labs develops compliance automation software for healthcare and life science companies. The platform is designed to help regulated organizations accelerate product development, reduce the cost and effort of meeting regulatory requirements, and maintain continuous audit readiness. Sierra Labs serves medical device manufacturers, pharmaceutical and biotech companies, and healthcare organizations, offering a unified compliance stack built to work alongside agile development workflows.

The company's team includes regulatory experts, engineers, DevOps specialists, and quality assurance professionals. Its stated mission is to simplify and automate compliance and quality management processes, and to decrease the cost and effort required to meet regulatory standards in the life science industry.

Core Platform Capabilities

• Automation: Reduces the time and effort required for compliance activities, with the goal of increasing productivity and supporting faster innovation.
• Traceability: Provides full traceability across the organization and generates compliance reports quickly to support certification efforts.
• Audit Readiness: Keeps organizations continuously compliant and prepared for audits at any time.
• Natural Language Processing (NLP): Uses NLP to suggest, process, and transform existing data into auditable compliance and regulatory documents.
• Integration: Connects with tools organizations already use to automate the publishing of compliance and regulatory documentation.

Key Products and Modules

• Sierra QMS (Quality Management System): A QMS tightly integrated with Atlassian Jira and other workflow tools, designed to maintain compliance throughout the agile development lifecycle. Conforms to 21 CFR Part 11 requirements, including electronic signatures and document export.
• Sierra Policies (Policy and Procedure Generator): A policy generator and regulatory database containing documentation templates for medical devices, ISO standards, HIPAA, sample SOPs, FDA requirements, EU regulations, and more.
• GxP Cloud Application and Infrastructure Validation: A cloud validation product that automates policy configuration and testing of Amazon Web Services (AWS) cloud infrastructure.

Regulatory Standards Supported

• 510(k): Medical device approval workflows and supporting documentation.
• ISO 13485: Quality management system requirements for medical devices.
• IEC 62304: Software as a Medical Device (SaMD) compliance.
• 21 CFR Part 820: Good Manufacturing Practice (GMP) for medical devices.
• 21 CFR Part 11: Electronic records and signatures for pharmaceutical and biotech workflows.
• GLP and GCP: Good Laboratory Practice and Good Clinical Practice standards.
• HIPAA / HITRUST: Digital health certification and patient data management.
• SOC 2: System and Organization Controls compliance.
• MDR: European Medical Device Regulation.
• GDPR: General Data Protection Regulation.

Industry Verticals and Use Cases

• Medical Device: Workflows for 510(k) submission preparation and quality records required for 21 CFR Part 820, ISO 13485, and IEC 62304.
• Pharmaceutical and BioTech: SOP tracking, GxP system inventories, and system/device lifecycle management aligned with 21 CFR Part 11, GLP, and GCP.
• Healthcare: Electronic patient data management in a HIPAA-compliant environment, with tracking of non-conformances, deviations, and CAPAs, and reporting to support HITRUST and SOC 2 certification.

Customer Examples

• Transparency Life Sciences: Used Sierra Labs to streamline quality documentation process automation and establish traceability within their QMS.
• Force Impact Technologies: A digital health company that used Sierra Labs to implement a QMS and automate compliance workflows in support of FDA approval.
• Rabble Health: Sierra Labs configured and deployed a HIPAA-compliant AWS cloud environment, drafted policies and procedures, and aligned processes with HIPAA standards within approximately two months.
• HZB Pharmaceuticals: Sierra Labs automated compliance workflows for GMP manufacturing and laboratory operations, reportedly reducing costs and expediting production by three times.

Deployment and Cost Reduction

• Cloud infrastructure validation is delivered on AWS, with automated policy configuration and testing.
• Sierra Labs states that companies typically spend more than 50% of their budget on GxP validation, and that its solutions can reduce that cost by a factor of three.
• Automation covers validation testing for devices, applications, web platforms, and custom off-the-shelf software, reducing the time and resources needed for testing, reporting, and approvals.
• The platform is designed to bridge the gap between IT, operations, compliance, and regulatory teams.

Sierra Labs is designed for healthcare and life science organizations of varying sizes, from early-stage companies seeking initial regulatory certification to established manufacturers managing ongoing GxP compliance programs.

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Software attributed to Sierra Labs

• Sierra Policies & ProceduresView
• Sierra Document AutomationView
• Sierra GxP Cloud ValidationView

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