Your Pharmaceutical Expert

The pharmaceutical industry is one of the most highly regulated industries in the world, where compliance is of the utmost importance not only to the companies who manufacture the products but the customers who depend on them for their life, health, and wellbeing. Clients in the pharmaceutical, biotech, and nutraceutical sectors require expert advice in the design, construction, and operation of their facilities. 

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Our Capabilities

  • Pharmaceutical process and manufacturing facilities 
  • Clean room environments 
  • Research laboratories 
  • Storage facilities 
  • Computer system validation 
  • Utilities design, commissioning, and validation 
  • Good Manufacturing Practices (GMP) with their regional interpretation by Therapeutic Goods Administration (TGA), Medsafe, and the National Pharmaceutical Council (NPC) 
  • United States Food and Drug Administration (USFDA), European Medicines Evaluation Agency (EMEA), International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), and Pharmaceutical Inspection Co-operation Scheme (PIC/S)  

Partnering with Synertec brings efficiencies and improved outcomes because we provide all GMP critical systems in-house under the one system of management, quality, and validation. 

Synertec’s experience in delivering large scale industrial solutions is supported by our commitment to security, adhering to ISO 27001, Information security, cybersecurity and privacy protection.

Get in touch today to see how Synertec could help with your next project.

Kylie Brailsford
Group Manager – Project Execution
[email protected]