Accessibility links Skip to main content

Pharmaceutical quality control and laboratory testing

  • Reliable quality control for batch release, raw materials and finished products
  • Chemical, physical and microbiological testing in accordance with GMP and ISO 17025

Request a quote

Fill out the form and we will contact you shortly.

Naam
Privacy Policy 

Contact us

Fill out the form and we will contact you shortly.

Naam
Privacy Policy 

Confidence in quality before market release 

Raw materials, active ingredients and finished products must demonstrably meet strict quality requirements before they can be released for manufacturing, distribution or market supply. 

Normec supports pharmaceutical companies, contract manufacturers and life sciences organisations with high-quality quality control and laboratory testing. From our certified laboratory, we perform a comprehensive range of analyses for pharmaceutical products, raw materials, excipients and medical devices. 

With more than 15 years of experience, we help organisations consistently ensure quality, safety and regulatory compliance. 

Quality control for batch release, import testing and finished products 

Effective quality control does more than ensure compliance. It also helps prevent delays, recalls and risks throughout manufacturing and distribution. 

Our testing services support: 

  • Batch release testing  
  • Import testing  
  • Finished product analysis  
  • Testing of active pharmaceutical ingredients (APIs)  
  • Chemical analysis  
  • Physical testing  
  • Microbiological testing  

We operate in accordance with GMP guidelines, DIN EN ISO 17025 accreditation and FDA registration. 

Comprehensive testing for pharmaceutical products and raw materials 

As part of pharmaceutical quality control, we perform a wide range of tests for both finished products and active pharmaceutical ingredients. 

Our analytical services include: 

  • Dissolution and disintegration testing  
  • Tablet hardness and friability testing  
  • Particle analysis and contamination testing  
  • pH, viscosity and conductivity testing  
  • Water content and moisture analysis  
  • Assay testing and impurity analysis  
  • Elemental impurities and trace metals analysis  
  • Sterility and endotoxin testing  
  • Bioburden, TAMC and TYMC testing  
  • Microorganism identification  

We also provide specialised analytical techniques, including UV-Vis spectrometry, infrared spectrometry, titration and microbiological analysis. 

Flexible planning and reliable turnaround times 

In the pharmaceutical industry, timing and reliability are critical. Delayed batch release or postponed analytical testing can have a direct impact on manufacturing schedules and product supply. 

That is why Normec works closely with planning and quality teams to organise testing programmes efficiently. We also provide flexible support for urgent requests and projects outside standard office hours. 

With our support, you can: 

  • Accelerate batch release activities  
  • Independently verify product quality  
  • Support successful product launches  
  • Improve production planning reliability  
  • Strengthen compliance and quality assurance  

Certified laboratory support 

Reliable test results begin with a robust quality management system. Our laboratory operates according to strict quality and safety protocols, supported by a comprehensive quality management system. 

Our experienced analysts, validated methods and advanced instrumentation deliver consistent, compliant results. Thanks to our expertise in the pharmaceutical and life sciences sectors, we support organisations throughout every stage of quality control and product release. 

Together, we help bring safe, reliable and high-quality pharmaceutical products to market. 

Would you like to know more about pharmaceutical quality control?

Frequently Asked Questions

Pharmaceutical quality control consists of laboratory testing used to verify the quality, safety and regulatory compliance of pharmaceutical products and raw materials. 

We test finished products, active pharmaceutical ingredients (APIs), raw materials, excipients and medical devices. 

Batch release is the process of verifying that a product meets all quality and regulatory requirements before it is released to the market. 

Yes. We provide sterility testing, endotoxin testing and microbiological contamination analysis, among other services. 

Our laboratory operates in accordance with GMP guidelines, DIN EN ISO 17025 accreditation and is FDA registered. 

Yes. We provide flexible scheduling and rapid testing services for time-critical projects. 

Independent quality control helps demonstrate product safety, regulatory compliance and product reliability.