A request for third-party laboratory testing to assess the safety, quality, and regulatory compliance of tablets acquired in India. Required testing includes verification of active pharmaceutical ingredients (API), screening for harmful contaminants (including heavy metals, microbial content, and chemical impurities), and assessment of biological activity and API stability. The analysis should confirm whether the tablets meet international safety and quality standards such as Good Manufacturing Practices (GMP). Please include a cost estimate for each test and note any additional testing recommendations relevant to pharmaceutical product integrity.
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