A safe and problem-free manufacturing process that is also as efficient as possible. This is both literally and figuratively vital for a pharmaceutical company. Our people are experienced in GAMP standards, matters such as batch control, the prevention of contamination, tracking & tracing, and the secure storage of data. Clear project design and detailed documentation provide additional guarantees in terms of safety and reliability. Our challenge is to also find opportunities for improvement whilst adhering to the stringent standards. We are also conversant with improvement methods such as Lean and Six Sigma.

Expertise from Strypes:

  • User Requirement Specification
  • Improving and expanding GAMP documentation
  • Functional Specification, Software / Hardware Design Specification
  • SDLC; Systems Development Life Cycle
  • Validation and qualification total GBS systems
  • Factory and Site Acceptance
  • Estimation, budgeting, design, tendering, constructing, testing and commissioning of new systems or buildings
  • Advice and implementation of data storage (PI) 

Installation of environmental controlling system

Medicines are produced and packed under strictly controlled conditions and to do so requires specialist technology. Erik van Noort is one of the pharm...

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Process automation in the pharmaceutical industry

Strypes is a valued partner for one of the biggest pharmaceutical concerns in the world in process automation. Here, Strypes employees work on a manuf...

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