Merit for Life Science with Microsoft Dynamics 365

 

Cloud-first ERP intentionally tailored for life science organizations.

Merit for Life Science is cloud-first ERP purposely built for biotech, pharma, and medical device manufacturers. It advances Dynamics 365 finance and operations to connect your entire organization:

  • Mapping resource qualifications to production requirements
  • Monitoring vendor relationships in procurement to help ensure quality standards are met in manufacturing
  • Providing your life science organization with visibility and transparency to deliver safe, innovative products
  • And much more

Your organization has unique needs and we understand them. Get the full picture of what we offer.

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, biotech, and medical device 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.

Make the Right Start

Get a pre-configured ERP solution that fits your journey.

Are you outgrowing your current accounting package? Struggling to meet investor expectations? You need a system that will let you grow unconstrained and run at peak productivity. You also have a budget to meet.

Get the cloud ERP for life science solution built to meet your needs today and for the days ahead.

Your business processes. Reimagined.

Transformation isn’t easy, but it’s necessary to grow, compete, and stay relevant. Our Catalyst Envisioning Workshops help your organization understand and prepare for disruptive changes that could impact your business and help you realize your most ambitious priorities. Topics include:

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.

-CFO of a Regulated Manufacturer in the Midwest

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.”

-IT Director of a multi-national service organization

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.

-VP and Head of IT of a West Coast Life Sciences Organization

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.

-CEO of a Southeast Life Sciences Organization

We are outcome-driven.

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