How Robust Solvent Documentation Supports Regulatory Submissions and Approvals

How Robust Solvent Documentation Supports Regulatory Submissions and Approvals

In the pharmaceutical industry, documentation is more than a regulatory formality, it is a pillar of product safety, quality assurance, and compliance. Every step in the drug development and manufacturing process must be documented with precision, and this holds especially true for solvents. As critical components in the production of active pharmaceutical ingredients (APIs) and […]

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Role of Acetone in Enhancing the Solubility of Poorly Soluble Drugs

Role of Acetone in Enhancing the Solubility of Poorly Soluble Drugs

In the pharmaceutical industry, drug solubility is a defining factor that directly influences the bioavailability, efficacy, and therapeutic potential of medicinal compounds. Despite decades of research and innovation, a significant proportion of new chemical entities (NCEs) continue to face challenges in formulation due to poor aqueous solubility. This presents a pressing concern for formulators aiming […]

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