We bridge pharmaceutical manufacturing, quality, and digital technology through practical, compliant, and scalable MES solutions.

DRIM Systems delivers MES implementation and digital manufacturing solutions for pharmaceutical companies, combining hands-on manufacturing knowledge with deep expertise in MES, electronic batch records, GMP, and pharmaceutical quality systems.

Technology alone does not digitalize a manufacturing process.

Successful pharmaceutical MES implementation requires a deep understanding of the process being digitized, the quality requirements governing it, and the technology executing it.

Manufacturing
Quality
Digital

DRIM connects all three.

What We Do

MES implementation, grounded in manufacturing and quality.

DRIM Systems is a pharmaceutical MES implementation specialist. Our work spans solution architecture, manufacturing process expertise, and the quality and compliance knowledge that makes a digital system defensible.

01

MES Implementation & Architecture

  • MES solution architecture
  • MES implementation
  • EBR / eBR design
  • MBR design and simplification
  • Recipe and workflow design
  • Process digitization
  • Functional specifications
  • Master data design
  • Testing and implementation support
  • Deployment and go-live support
  • MES optimization
02

Pharmaceutical Manufacturing

  • Manufacturing process analysis
  • Process mapping
  • Process decomposition
  • Workflow optimization
  • Equipment and material flows
  • Batch manufacturing
  • Manufacturing execution design
  • Digitalization of shop-floor processes
03

Quality & Compliance

  • GMP requirements translated into MES functionality
  • Data Integrity
  • FDA 21 CFR Part 11
  • EU GMP Annex 11
  • EU GMP Annex 15
  • EU GMP Annex 16
  • GAMP 5
  • CSV / validation
  • Electronic batch records
  • Review by Exception
  • Batch certification / QP perspective
The Difference

The Difference Is in the Bridge

Pharmaceutical MES sits at the intersection of manufacturing, quality, and technology. DRIM understands all three.

Our consultants combine practical pharmaceutical manufacturing experience with MES solution architecture and pharmaceutical quality expertise. This enables us to translate real manufacturing processes and GMP requirements into digital workflows that are practical for operators, meaningful for Quality, and technically robust.

Manufacturing → Quality → MES

Our experience spans pharmaceutical manufacturing environments across the globe, supporting MES design, EBR implementation, process mapping, digital manufacturing, and deployment preparation.

About Us

About DRIM Systems

DRIM Systems is a pharmaceutical consulting company focused on MES implementation and digital manufacturing. We help pharmaceutical manufacturers translate complex production processes, quality requirements, and regulatory expectations into practical digital manufacturing solutions.

Our approach combines pharmaceutical domain expertise with hands-on MES experience, allowing us to work effectively across Manufacturing, Quality, Engineering, Automation, and IT.

Our role is to bridge the gap between how pharmaceutical manufacturing works, how it must be controlled, and how it can be digitally executed.
Our Approach

End-to-end MES implementation support.

01

Understand

Understand the manufacturing process, business requirements, and quality expectations.

02

Design

Translate requirements into MES architecture, workflows, recipes, and EBR structures.

03

Implement

Configure, test, validate, and deploy the solution.

04

Optimize

Improve usability, process efficiency, data integrity, and digital execution.

Contact

Let's Discuss Your MES Project

Whether you are planning a new MES implementation, preparing for digital manufacturing, or looking to optimize an existing EBR environment, let's discuss how DRIM Systems can support your project.

Company
DRIM Systems
Address
Cerska 2A
Belgrade, Serbia