Deliver innovative, effective
and safe products
with finance and operations software
tailor-made for life science manufacturers.
Merit for Life Science advances
the finance and manufacturing (ERP)
capabilities of Microsoft Dynamics 365
Delivering an industry-tailored solution that meets the
rigorous requirements of pharma and biotech companies.
With Merit for Life Science, you can drive increased process efficiencies, ready for and support rapid growth, and drive
valuation while maintaining FDA CFR 21 part 11, EMA Annex 11, and other country-specific regulatory compliance.
Finance
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.
Procurement
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.
Material Management and Control
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.
Production/Manufacturing
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.
Regulatory Compliance
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.
Quality (QMS)
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.
Finance
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.
Procurement
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.
Materials Management and Control
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.
Production/Manufacturing
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.
Regulatory Compliance
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.
Quality (QMS)
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.
Discover all the ways life science organizations
succeed with Merit Solutions.
Merit provides our organization with value we couldn’t match elsewhere: a strong implementation process and the ability to serve as our sole partner for our end-to-end digital technology needs.
Merit developed an elastic and powerful architecture from scratch by leveraging cutting-edge Microsoft technology like Azure and the cross-platform mobile platform Xamarin…effectively making the solution “future proof.”
When evaluating system integrators in the Life Sciences space, we found that only Merit had the depth of Life Science industry experience we expected, references that were rock solid, and a string of account “saves” that were undeniable. It made for an easy choice – Merit Solutions.
The Merit Team didn’t just get the job done, they got it done on time and provided quality deliverables which were critical in ensuring efficiency, effectiveness, and compliance.