Improve your decision-making process with reliable, auditable accounting practices. Establish financial reporting standards for acquired entities or to prepare for acquisition. Ensure compliance with GAAP, IFRS, SOC1-3 Sarbanes-Oxley and the Sunshine Act.

Audit and qualify vendors with precision based on industry protocols. Digitally control and oversee orders without interrupting production. Manage materials with advanced retest capabilities, automated label printing, and a streamlined overview of key inventory data.

Electronically manage and document everything from materials evaluation and potency to equipment calibration and device/batch history records, across multiple modes of manufacturing. Track the handling of raw materials throughout their preparation stage, capturing information about the process digitally and ensuring everything is auditable and done according to SOPs and specific batch requirements.

Leverage an extensible digital framework that simplifies your process of meeting FHIR, HIPAA, and GxP requirements, as well as ensures 21 CFR Part 820 and 21 CFR Part 11 compliance. Provide functionality to address: compliance, quality, shelf life and retest, CAPA, controlled labels, electronic batch records, audit management, weighing and dispensing, and instrument calibration.

Improve your decision-making process with reliable, auditable accounting practices. Establish financial reporting standards for acquired entities or to prepare for acquisition. Ensure compliance with GAAP, IFRS, SOC1-3 Sarbanes-Oxley and the Sunshine Act.

Audit and qualify vendors with precision based on industry protocols. Digitally control and oversee orders without interrupting production. Manage materials with advanced retest capabilities, automated label printing, and a streamlined overview of key inventory data.

Track and store inventory in multiple units of measure, and identify the amount of active ingredient each unit contains. Identify the location of every component wherever it is—in stock, in finished goods, or at a customer’s site—with serial and lot numbers. Track the handling of raw materials throughout their preparation stage, capturing and storing information about the process and ensuring everything is auditable and done according to SOPs and specific batch requirements.

Leverage an extensible digital framework that simplifies your process of meeting FHIR, HIPAA, and GxP requirements, as well as ensures 21 CFR Part 820 and 21 CFR Part 11 compliance. Provide functionality to address: compliance, quality, shelf life and retest, CAPA, controlled labels, electronic batch records, audit management, weighing and dispensing, and instrument calibration.

Manage various quality test points throughout the materials and production process. Track and manage all complaints, incidents, significant deviations, adverse events and material or process non-conformances, including alerts and notifications on stages. Prove a validated environment by establishing documented evidence of system and process consistency for intended use.