Pharmaceutical products must meet strict regulatory requirements to ensure their safety, efficacy, and quality. Analytical testing plays a crucial role in maintaining compliance with these regulations by verifying the chemical composition, potency, and purity of drugs.
Regulatory bodies require thorough documentation of analytical testing procedures, results, and validation processes. Companies must adhere to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to ensure continuous compliance.
By integrating robust analytical testing into the pharmaceutical manufacturing process, companies can avoid compliance risks, product recalls, and regulatory penalties.
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