Our Services
With ImageProVision, you're sure of precision and accuracyOur Innovation Hub
Our range of sample analysisservices offers accurate and reliable sample testing and evaluation for pharmaceutical industry. With state-of-the-art equipment and expert technicians, we provide thorough and precise analysis of samples, including chemical composition, material properties, product quality, and more. Trust our services to ensure compliance, optimize processes, and make informed decisions based on reliable data
- PSD Analysis
- Morphological study
- Particle Classification (API, Excipient, Globule classification)
- Reverse Engineering
- Particulate matter counts
- Nano Particle analysis
- Hot stage microscopy
- Seam Analysis
Our calibration and validation services ensure the accuracy and reliability of your measurement instruments and processes. Our team of skilled technicians performs meticulous calibration to verify the performance of your equipment and ensure traceability to national standards.
- Re-Certification of calibration slide
- Calibrate system
- Validate system
Our method development service offers customized solutions for analytical method development to meet your specific testing needs. Our experienced team works closely with you to design and optimize analytical methods, considering factors such as sample type, sensitivity, accuracy, and efficiency.
- Method preparation for various dosage forms
- Assistance and training
Our comprehensive training provides both onsite and online options to help users effectively utilize ImageProVision software solutions. Our experienced trainers deliver hands-on training sessions tailored to your specific needs, ensuring you gain proficiency in image analysis, data interpretation, and software functionality. Whether through in-person sessions or virtual, we empower users to maximize the capabilities of ImageProVision and optimize their particle/sample analysis workflows.
Our consultation service offers expert guidance and support in addressing FDA queries related to particle analysis. Our team provides in-depth knowledge of FDA regulations and requirements, assisting you in formulating comprehensive and accurate responses to queries related to particle size and shape, morphology, contamination, and quality control. Trust our expertise to ensure compliance with FDA standards and streamline your regulatory processes.
We offer expert assistance in identifying the root cause of batch-to-batch variation and other related issues. Our specialized services help uncover the underlying factors and provide valuable insights for resolving these challenges effectively. Contact us for reliable support in pinpointing the root cause and achieving consistent product quality.
- Batch-to-Batch Variation
- Variation in dissolution
Our specialized services focus on assisting clients in obtaining ANDA (Abbreviated New Drug Application) approval for their pharmaceutical products with a strong emphasis on particle analysis. We offer comprehensive support in developing robust analytical methods, conducting particle size distribution studies, addressing formulation challenges, and ensuring compliance with FDA regulations
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