Danish IT consulting for the manufacturing and pharmaceutical industry

Introduction

Pharma and production companies in Denmark operate under strict requirements for documentation, operational reliability, and compliance. Therefore, they need an IT provider that not only understands technology—but also the regulated context. At Hyperbolic, we offer IT consulting and solutions that bridge the gap between technology and regulatory requirements.

What is IT consulting?

IT consulting is about matching technology with business goals and regulatory requirements. In regulated industries, this entails:

• GxP validation and documentation

• Risk assessment and audit preparation

• Designing stable and scalable system architectures

• Integration with existing production systems (MES, SCADA, ERP)

Hyperbolic acts both as a strategic advisor and a provider of software development and integration.

Our services

We assist, among other things, with:

• Design and development of scalable IT solutions

• Review of existing systems and gap analysis

• Preparation for audits and inspections

• Integration with production equipment and databases

We closely collaborate with QA, IT, and production, ensuring that the solutions are both technically robust and compliant.

Who uses Hyperbolic?

We work with:

• Pharmaceutical and biotech companies

• Food production and process industries

• Manufacturing companies with high quality requirements

Our approach

1. Pre-analysis and regulatory assessment

2. Architecture and design with documentation

3. Development and testing

4. Support and validation

We always work closely with your internal teams and document the process from start to finish.

FAQ

Do you offer consulting without development?
Yes. We also provide independent consulting on strategy, specification requirements, and audits.

Do you have experience with GxP and validation?
Yes. We have worked with GAMP5, CFR21 Part 11, and relevant EU requirements. Documentation follows industry standards.