Batch and Lot Release Potency Testing

AskPharma's Batch and Lot Release Potency Tests confirm the purity, potency, and identity of a product.
Batch and Lot Release Potency Testing is essential to ensure that every manufactured product consistently meets cGMP requirements for safety, purity, potency, and identity. At AskPharma, we provide independent, ISO 17025-certified and FDA-registered testing services to verify compliance with regulatory standards, protect product integrity, and build consumer trust. Our experienced MDs, PhDs, and chemists utilize validated, compendial, and client-transferred methods, as well as custom method development when needed, to deliver precise and reliable results. With our proven expertise, advanced instrumentation, and fast turnaround times, AskPharma helps you bring high-quality products to market with confidence.

Raw Material Testing

The experts at AskPharma lnc. perform analysis on materials to determine their:


⦿ Identification
⦿ Purity
⦿ Vitamins
⦿ Botanic Ingredients

Method Development, validation, & verification

AskPharma lnc. provides precise, consistent, robust, stability-indicating and cost-effective analytical methods to our customers.
Key Parameters Include:
⦿ Specificity
⦿ Linearity
⦿ Limit of Detection and Quantitation
⦿ Accuracy
⦿ Precision
⦿ Robustness
⦿ Solution Stability

Stability Studies

At AskPharma, our stability studies generate the data needed to establish product shelf life and expiration dates. Finished products are stored in state-of-the-art controlled environmental chambers and tested at protocol-defined timepoints. These chambers simulate real-world conditions of temperature and humidity across different global regions. For accelerated studies, higher temperature and humidity settings are applied to provide early insights into potential long-term stability issues. With precise monitoring and expert analysis, AskPharma ensures reliable results that support product quality and regulatory compliance.

Impurity Profiling

At AskPharma, we provide comprehensive impurity profiling services to safeguard the purity, safety, and quality of APIs, excipients, and finished products. Since many impurities are present only at trace levels within complex matrices, highly sensitive and specific analytical methods are essential. Our laboratory is equipped with advanced LC-MS systems, allowing accurate identification and quantification of impurities down to sub-parts per billion (ppb). These capabilities are critical for detecting nitrosamines, extractables and leachables, polyfluoroalkyl substances (PFAS), residual solvents, and other regulated contaminants. Backed by the expertise of our MDs, PhDs, and senior chemists, we develop, validate, and apply robust analytical methods that comply with global regulatory requirements. AskPharma delivers precise, reliable, and timely impurity data to support compliance, ensure product integrity, and strengthen consumer trust.

Consulting Services

Consulting & Lab Services: AskPharma Inc. helps you understand testing requirements and achieve your product development goals. Our team provides expert guidance on chemical, formulation, and technical challenges across diverse product forms, applications, active ingredients, and packaging options.