In the pharmaceutical and medical sectors, the quality and specifications of active ingredients are critical. Povidone Iodine (PVPI) is no exception, with stringent standards governing its production and use. Understanding these specifications is vital for ensuring efficacy and safety in medical applications, from topical antiseptics to advanced pharmaceutical formulations.

The article highlights key specifications for PVPI, including its 'Medicine Grade' standard, 'Loss on Drying' (NMT 8%), 'Heavy Metals' (NMT 20ppm), and pH range (1.5-5.0). Nitrogen content is typically between 9.5%-11.5%, and available iodine content usually ranges from 9.0%-12.0%. These parameters, often verified against standards like USP, BP, EP, and CP, ensure that the PVPI meets the high purity and performance requirements for medicinal use.

Certifications such as GMP, CEP, DMF, ISO, KOSHER, and HALAL are crucial indicators of a manufacturer's commitment to quality and regulatory compliance. These certifications provide assurance to pharmaceutical companies and healthcare providers that the PVPI they source meets international standards for safety, efficacy, and manufacturing practices. The availability of such certifications is often a key factor in supplier selection.

The production capacity, often measured in metric tons per year, indicates a manufacturer's ability to meet market demand. For pharmaceutical companies requiring large volumes of PVPI, partnering with suppliers who have robust production capabilities and a reliable supply chain is essential. The consistent quality and competitive pricing of PVPI also play a significant role in its widespread adoption in various medical products.

In essence, the meticulous adherence to specifications and certifications for PVPI is fundamental to its role in developing safe and effective pharmaceutical products. This focus on quality ensures that PVPI can continue to be a trusted agent in wound care, disinfection, and various other critical medical applications.