Analytical Capabilities

Development, Validation, & Transfer of Test Methodologies:

1. Full Method Development: Our analytical experts excel in crafting methodologies tailored to specific pharmaceutical requirements. From conceptualization to execution, we ensure the development of comprehensive and robust analytical methods.

2. Method Transfer/Evaluation: Seamless transfer and evaluation of methods are crucial for maintaining consistency. Espi’s analytical team ensures a smooth transition, evaluating and transferring methods with precision.

3. Optimization of Existing Methods: Continuous improvement is key to our analytical services. We optimize existing methods to enhance efficiency, accuracy, and relevance to industry standards.

4. Validation of Developed and Transferred Methods: Validation is at the core of our analytical processes. Whether it’s a newly developed method or a transferred one, we validate with meticulous attention to detail, ensuring reliability and compliance.

GLP Approved Analytical Lab: A Hub of Excellence

Our facility boasts a fully-fledged GLP approved Analytical Lab, subdivided into three specialized sections:

1. Wet Lab: Equipped with cutting-edge technology, our wet lab ensures accurate and precise wet chemistry analysis. It is the foundation for reliable results in our analytical services.

2. Instrumentation: Our Instrumentation section houses state-of-the-art equipment in line with current industry requirements. From HPLC’s to AAS or Texture Analyser’s, each instrument is chosen for its precision and efficiency.

3. Microbiology: In the Microbiology section, we conduct analyses that adhere to the highest standards. Our microbiological testing ensures the safety and compliance of our pharmaceutical products.

Advanced Equipment & Data Integrity:

Our commitment to precision is mirrored in our choice of equipment. The HPLC and AAS instruments are interconnected through a central server, guaranteeing data integrity. This connectivity ensures that our analyses are not only accurate but also meet the highest standards of reliability.

Beyond Routine Analysis: Method Development & Analytical Method Validations:

Our analytical lab goes beyond routine analyses. We specialize in method development and analytical method validations, including impurity profiling. This expertise ensures that our clients receive comprehensive insights into the quality and characteristics of their pharmaceutical products.

At Espi Industries & Chemicals, our Analytical Capabilities are not just services; they are a commitment to excellence, precision, and reliability. Join us in exploring a realm where every analysis is a testament to our dedication to pharmaceutical excellence.