Quality Control Solutions

  1. Digitalize Your Validation Procedures For Microbial QC Testing 9/28/2023

    Discover a 21 CFR Part 11-compliant digital validation platform designed for conducting IQ & OQ on your microbial QC testing systems dedicated to bioburden testing, sterility testing, and air monitoring.

  2. Analytical Services 10/23/2024

    Upperton offers analytical services designed to support the development, monitoring, and quality control testing of pharmaceutical products.

  3. Detection Of Endotoxin And Non-Endotoxin Pyrogens By MAT 4/4/2022

    Performing endotoxin testing? Trust your data with a Monocyte Activation Test that mimics the human immune reaction and detects both endotoxins and non-endotoxin pyrogens.

  4. Tailored Process Development Services Designed For Success 8/6/2024

    Explore the design services offered by the Gibco Media by Design team including cell line development, media and feed panel evaluations, bioproduction analytics and more.

  5. HPAPI Pharmaceutical Compacting And Coating Enclosure With Rolling Cart 4/3/2019

    Advantech Sonic Sifter Powder Weighing and Transfer Enclosure designed to provide personnel protection during compacting and coating operations involving Highly Potent Active Pharmaceutical Ingredients (HPAPI).

  6. Analytical Method Development And Validation 7/29/2024

    In pharmaceutical testing, the development and validation of analytical methods are absolute musts when it comes to reliable quality control. Natoli Scientific is at the forefront of offering comprehensive analytical method development and validation services designed to ensure the integrity of your company’s drug formulations. Our expert team develops robust methods tailored for each unique compound, with an approach that emphasizes precision, accuracy, sustainability, and compliance with regulatory standards such as the FDA and ICH guidelines. These methods are meticulously validated to confirm their reliability across a range of analytical parameters including specificity, sensitivity, linearity, and reproducibility.

    This validation process is critical for verifying that our methods produce consistent, trustworthy results throughout the product’s lifecycle, thus fostering confidence in the safety and efficacy of pharmaceutical products.

  7. FlexUP Technology Renewal Program 4/11/2022

    Are you using obsolete or aging instruments simply because they continue to work? Running your laboratory with outdated technology brings about challenges beyond just headaches. Older technology may limit your performance, increase your costs, and open your lab up to risk. It may be time to investigate the real cost of using obsolete technology.

    With the Waters FlexUP Technology Renewal Program, always work with the latest technology for optimum productivity and security.

  8. Used Perkin Elmer Paragon 1000 PC FT-IR Spectrometer 6/6/2019

    Used Perkin Elmer Paragon 1000 PC FT-IR Spectrometer, benchtop design, serial# 38716.

  9. API/HPAPI Containment Solutions For Pharmaceutical Manufacturing 3/27/2019

    Solve your containment challenge by working with a company that understands your process, CPT, expectations, facility allowances and restrictions as well as specific equipment specifications.

  10. HPAPI Package Inspection Enclosure 3/26/2019

    The HPAPI Package Inspection Suite is designed to provide personnel and product protection down to a respiratory exposure of at least 100 micrograms per cubic meter air (100 ug/m3). Package inspection operations involve manipulation of highly potent pharmaceutical ingredients (HPAPI), such as fentanyl.