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Digital Transformation in Pharma Industry

We specialize in Computerized System Validation (CSV) and Quality Assurance (QA) support services to our global customers in the life-sciences industry.

// Pharma digital transformation - the first step

Each Vimachem digital transformation project starts with an assessment of the customer digital maturity.

Each Vimachem digital transformation project begins with an assessment of the customer’s digital maturity. This evaluation is structured around three clearly defined business dimensions:

Technology

Assessing the existing technological infrastructure, digital capabilities, and integration readiness.

Operations

Evaluating processes, workflows, and efficiency to identify areas for digital optimization.

Organization & culture

Reviewing the company's culture, leadership alignment, and readiness to embrace digital change.

// How it works

Digital maturity assessment

A powerful tool for digital pharma transformation

The Digital Maturity Assessment serves as a crucial tool, providing clear guidelines for navigating the digital transformation journey in pharma.

Identifying opportunities through gap analysis

Leveraging insights from the Digital Maturity study, our Pharma 4.0 experts collaborate closely with site-level teams to conduct a gap analysis. This process quickly identifies areas for improvement, highlighting key opportunities to enhance digital transformation in the pharmaceutical industry.

Activating digital transformation with pilot projects

The discovered opportunities are then used to initiate digital transformation pilot projects, ensuring a structured and efficient approach to digital transformation in pharma manufacturing.

Scaling pilot projects for full-scale benefits

At Vimachem, we understand that digital transformation in biopharma and pharmaceutical digital transformation doesn't require a full-scale plant overhaul. Instead, some of the most impactful results come from pilot projects targeting underperforming operational units, transforming those units and then optimizing and scaling across lines and sites.

By successfully implementing pilot projects, organizations can scale up these initiatives to maximize the benefits of digital transformation in the pharma industry. A well-defined scale-up strategy is essential to ensure long-term success in biopharma digital transformation.

What it is like working with Vimachem

See all case studies

Sharp Sterile Establishes a Foundation for Multi-Site Manufacturing Analytics with Vimachem's OEE Platform

Sharp Sterile Manufacturing

Pharmaceutical Manufacturing

2 months

Implementation time

2 lines

Sterile fill-finish

Read case study

How Purna Pharmaceuticals N.V. Implemented Vimachem SSM Level 3 and Level 4 to Support Multi-Client Liquid and Cream Packaging

Purna Pharmaceuticals N.V. (Contract Manufacturer)

Pharmaceutical Manufacturing (CDMO)

Level 3 + 4

Serialization and reporting

5 lines

Serialization-equipped, of 15 total

Read case study

From Paper-Based to Scalable Serialization! How Fulton CDMO Standardized on Vimachem Level 3 SSM & Manual Aggregation Module to Enable Compliance and Growth

Fulton Medicinali (CDMO)

Pharmaceutical Manufacturing (CDMO)

12 weeks

To go-live

7 tickets

Support tickets in two years

Read case study

Labatec Achieves a 30% OEE Increase (86% Relative Improvement) and 324% ROI with Vimachem's Manufacturing Analytics and OEE Solution

Labatec

Pharmaceutical Manufacturing

+30 pts

OEE increase

324%

ROI

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From 41% to 65% OEE! A 59% Increase - Inside Astrea Pharma's OEE Breakthrough on their First Production Line with Vimachem's MA & OEE.

Astrea Pharma

Pharmaceutical manufacturing

41 to 65%

OEE on the first line

59%

Relative increase

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How ELPEN Increased OEE by 90% and achieved 299% ROI with Vimachem's Manufacturing Analytics & OEE solution

ELPEN

Pharmaceutical manufacturing

90%

OEE increase

299%

ROI

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Ensure On-Time Drug Shipments: How to Quickly Replace Your Serialization System with the Leading Track-and-Trace Platform

HELP Pharmaceuticals

3 months

Full L3 to L5 replacement

Zero

Production downtime during cutover

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Serialization Compliance in Russia with Medice and Wipotec

MEDICE Arzneimittel Pütter GmbH & Co. KG

3 weeks

Average time to upgrade for market compliance

Zero

Line stoppages to test the integration

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Serialization Driving Innovation & Change With RFID

Fresenius Kabi

15 to 30 min

Manual tray check before RFID

250 vials

Read in a single pass after RFID

Read case study

Serialization For Global Medicines Traceability

Aspen Pharmacare Australia

10

Export markets supported

5

Packaging lines serialized

Read case study

Pharma Trackts 2021 | Serialization Driving Change And Innovation

IBERFAR, Indústria Farmacêutica S.A.

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// Pay only for what you need

Flexible and cost-efficient pharma digital transformation

Our modules are designed for flexibility and cost-efficiency, allowing you to pay only for the features you truly need.

These modules can be deployed as standalone solutions, offering end-to-end functionality across both manufacturing and quality operations. This modular approach gives you the flexibility to select only the software components required for your specific needs, enabling you to digitalize your production step by step as part of your pharmaceutical digital transformation.

This scalable model supports your digital transformation in pharma manufacturing and ensures a smooth transition towards full digital transformation in pharmaceuticals, at a pace that works best for your organization.

Benefits of pharma digital transformation

65%

Reduction in deviations

35%

Increase in OEE of packaging lines

30%

Reduction in changeover time

Ready to augment your shop floor operations?

Request a demo