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Netpharmalab (EN) | Pharmaceutical Analytical Services Netpharmalab (EN) | Pharmaceutical Analytical Services
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    • Extractables and Leachables studies
    • Toxicological risk assessment of extractable and leachable impurities
  • Biological Products
    • PK/PD bioanalysis and immunogenicity
    • Advanced characterization HRMS
    • Cell-based bioassays
    • Cell viability and cytotoxicity
    • DNA and protein analysis
    • Gene expression analysis
    • Purity and stability studies
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    • Microbiology
      • Bacterial endotoxins test
      • Non-sterile products microbiological analysis
      • Growth promotion test for culture media
      • Disinfectants qualification
      • Development and validation of microbiological methods
      • Bioburden testing
      • Efficacy of antimicrobial preservation
      • Sterility Test
      • Microbiological identification
      • Particle counting and environmental monitoring
    • Physicochemical analysis
      • Test of Nitrosamines
      • Analysis of elemental impurities (ICP-MS)
      • Routine analysis during pharmaceutical development phase
      • Quality control and release of raw materials and finished products
      • Development of analytical methods
      • Validation of analytical methods
      • Identification and quantification of unknown impurities (LC-MS y GC-MS)
    • Mutagenic Impurities and Nitrosamines
    • Stability studies
      • In-use stability studies
      • ICH stability studies (Zones II to IVb)
      • Ongoing stability studies
      • Pre-stability studies
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  • Galenical Development
    • Lyophilization of Pharmaceuticals
    • Sterile and non-sterile liquid forms
    • Semi solid dosage forms
  • Extractables & Leachables
    • Extractables and Leachables studies
    • Toxicological risk assessment of extractable and leachable impurities
  • Biological Products
    • PK bioanalysis and immunogenicity
    • Advanced characterization HRMS
    • Cell-based bioassays
    • Cell viability and cytotoxicity
    • DNA and protein analysis
    • Gene expression analysis
    • Purity and stability studies
  • Testing
    • Microbiology
      • Bacterial endotoxins test
      • Non-sterile products microbiological analysis
      • Growth promotion test for culture media
      • Disinfectants qualification
      • Development and validation of microbiological methods
      • Bioburden testing
      • Efficacy of antimicrobial preservation
      • Sterility Test
      • Microbiological identification
      • Particle counting and environmental monitoring
    • Physicochemical analysis
      • Test of Nitrosamines
      • Analysis of elemental impurities (ICP-MS)
      • Routine analysis during pharmaceutical development phase
      • Quality control and release of raw materials and finished products
      • Development of analytical methods
      • Validation of analytical methods
      • Identification and quantification of unknown impurities (LC-MS y GC-MS)
    • Mutagenic Impurities and Nitrosamines
    • Stability studies
      • In-use stability studies
      • ICH stability studies (Zones II to IVb)
      • Ongoing stability studies
      • Pre-stability studies
  • Consulting & Import
    • Analytical consulting services
    • Galenical consulting services
    • Import laboratory
    • Toxicology
  • Contact
  • About us
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News

Home News

How to choose the righ external laboratory for pharmaceutical testing

13 June, 2025

By laura


Why is it crucial to choose the right external laboratory for pharmaceutical testing? Outsourcing pharmaceutical testing to external laboratories has…

Read more

Netpharmalab strengthens its position with the acquisition of Docuchem

12 June, 2025

By admin_netpharmalab


Netpharmalab strengthens its presence in the pharmaceutical sector with the acquisition of Docuchem Netpharmalab, a subsidiary of the AGQ Labs…

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Impact of the new ICH guidelines on quality control laboratories

6 June, 2025

By laura


Regulatory evolution of ICH guidelines and their direct influence Quality control laboratories play an essential role in the pharmaceutical industry,…

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The importance of bioequivalence studies in the pharmaceutical industry

4 June, 2025

By laura


Bioequivalence studies in generic drugs In the pharmaceutical field, ensuring the safety and efficacy of drugs is an absolute priority….

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Analysis of active ingredients for the production of medicines

4 June, 2025

By laura


An essential process in the modern pharmaceutical industry In the pharmaceutical industry, the analysis of active ingredients is a critical…

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Stability Studies in Pharmaceuticals

13 March, 2025

By admin_netpharmalab


What are they, what types are there, and why are stability studies in pharmaceuticals key in the pharmaceutical industry? Stability…

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Mass Spectrometry in Drug Development Applications

10 March, 2025

By admin_netpharmalab


Inductively Coupled Plasma Mass Spectrometry (ICP-MS) ensures drug safety and regulatory compliance in the pharmaceutical industry What is Inductively Coupled…

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Extractables and Leachables study: protect your product from the packaging

12 February, 2025

By admin_netpharmalab


Protect your product from the packaging with the study of Extractables and Leachables, comply with international regulations and guarantee its…

Read more

Bioburden Analysis for Pharmaceutical Safety and Quality

30 December, 2024

By admin_netpharmalab


Importance of Bioburden Analysis in the Pharmaceutical Industry, Its Key Methods, and How It Ensures Product Safety and Quality Bioburden…

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Microbiological analysis of pharmaceutical products

30 December, 2024

By admin_netpharmalab


Microbiological analysis of pharmaceutical products ensures the safety and quality of medicines reaching the market Microbiological analysis of pharmaceutical products…

Read more

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  • Phone: +34 91 088 3733
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