The Good Manufacturing Practice (GMP) is a set of guidelines and regulations that ensure the quality, safety and efficacy of products in the pharmaceutical and medical industries. GMP provides a systematic approach to manufacturing processes and quality assurance, including the production of active substances, which are the essential components of medicines and other pharmaceutical products. GMP regulations cover all aspects of production. From raw material sourcing and handling to final packaging and labeling. Compliance with GMP regulations is essential for ensuring the quality and safety of pharmaceutical and medical products. Therefore, Sasma’s adherence to GMP guidelines for the production of its alcohols and spirits ensures that we meet the quality requirements of the pharmaceutical and medical industries.

Sasma offers different types of alcohol for the production of pharmaceutical and medical products. We offer regular grade alcohol which can be used for the production of medicinal drugs, homeopathic products, disinfectants and extracts. We also offer injectable grade alcohol which is sterile pure ethanol used for injection purposes.

Sasma’s alcohol products used in the pharmaceutical and medical industry have specific storage and transportation requirements to maintain their quality and purity. These requirements may vary depending on the type of alcohol and the specific needs of the client. It is important to store the alcohol in a cool and dry place, away from direct sunlight and heat sources. Transportation should also be carefully managed to prevent any exposure to extreme temperatures or physical damage. Sasma may provide further guidance and recommendations based on the specific product and client needs.