Batch & Lot Testing
Batch/Lot Testing for Release Batch and lot testing for release are critical steps in ensuring the quality and consistency of pharmaceutical tablets. Natoli Scientific provides comprehensive batch testing services that align with stringent industry standards and regulatory requirements. Each lot undergoes a rigorous analysis to verify that it meets predefined specifications for weight, tablet breaking […]
Analytical Method Development and Validation
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 […]
USP Tablet Compression Characterization
Natoli Scientific takes pride in its comprehensive USP<1062> Tablet Compression Characterization services, tailored to address the complexities of tableting in pharmaceutical manufacturing. Staying true to the parameters outlined in the United States Pharmacopeia (USP) Chapter 1062, our approach meticulously evaluates tablet compression behaviors. By thoroughly characterizing the compression profile, we can pinpoint the optimal compression […]
Stability Testing – Onsite Preclinical Services to Support Your Product Development
Natoli Scientific’s preclinical stability studies represent a critical facet of our pharmaceutical testing services, providing essential data on the shelf life and storage conditions of drug candidates. These studies are expertly designed to evaluate physical, chemical, and microbiological stability, ensuring that formulations retain their safety, efficacy, and quality over time. Our state-of-the-art facilities simulate various […]
OnSite Preclinical Services to Support Your Product Development
STABILITY TESTING Natoli Scientific’s preclinical stability studies represent a critical facet of our pharmaceutical testing services, providing essential data on the shelf life and storage conditions of drug candidates. These studies are expertly designed to evaluate physical, chemical, and microbiological stability, ensuring that formulations retain their safety, efficacy, and quality over time. Our state-of-the-art […]
A Closer Look at Tabletability, Compactibility and Compressibility
A Closer Look at Tabletability, Compactibility, and Compressibility In the realm of pharmaceutical manufacturing, the process of tablet compression is a critical step that ensures the correct dosage and stability of the medication. Natoli Scientific stands at the forefront of this field, conducting comprehensive compression studies that delve into the development of profiles for tabletability, […]
Leaders in Tablet Characterization and Methodologies: A Brief History of Natoli Scientific & USP
What is USP <1062>? USP <1062> is a universally recognized standard put forth by the United States Pharmacopeia, providing in-depth details about the regulations and fundamentals of tablet characterization. It provides detailed insights into key aspects such as porosity, tensile strength, and compactibility. Porosity, essentially, indicates the air content in a tablet post-compression, while tensile […]