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Pharmaceutics And Cosmetics Ingredients Product Applications In Usa
8 applications found
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Within the globalized pharmaceutical raw material supply chain, there is an increasing public health concern of raw material adulteration, contamination, or mislabeling, especially with recent incidents such as the adulteration of heparin. This has driven regulatory bodies to update their guidelines. Chapter 5.33 of the latest GMP guidelines for Medicinal Products for Human Use, provided by the European Commission (EC), entitled "Eudralex," specifies that "there should be appropriate procedures or measures to ...
ByGalaxy Scientific Inc based in Nashua, NEW HAMPSHIRE (USA)
Pharmaceutical applications for ion exchange resins and polymeric adsorbents used in other industries but with the added requirements for certification and validation. The resins can be used as active pharmaceutical ingredients and excipients, and as water treatment media. Other applications include extraction and purification of enzymes, hormones, alkaloids, viruses, antibiotics streptomycin, penicillin, and treatment of fermentation products, ...
BySuzhou X Chemical Co.,Ltd based in Suzhou City, CHINA
Efficient recovery of active pharmaceutical ingredients (APIs), chemical substances or food powders after drying applications such as spray and fluid bed drying is frequently a problem. The same problem occurs in many milling and micronization applications. The preferred way to recover these sensitive products is with cyclone collectors due to their direct powder capture. Unlike bag filters or wet scrubbers, cyclones minimize filter or product contamination and product cross contamination and can easily handle a ...
ByAdvanced Cyclone Systems, S. A. (ACS) based in Porto, PORTUGAL
Formulation is a major component in the efficacy of a drug. Formulation involves the preparation/mixture of an active pharmaceutical ingredient in/with a physical carrier (i.e., a tablet, spray, inhaler, or syrup) to insure adequate efficacy, delivery, and stability. Heavily used in formulation, polymeric excipients such as copovidone (PVP/VA64) can serve various functions when added to API such as matrix former, binding agent or sustained release ...
BySpectra Analysis Instruments, Inc. based in Marlborough, MASSACHUSETTS (USA)
Efficient recovery of active pharmaceutical ingredients (APIs) or final product formulations (FPFs) after a spray dryer can be quite challenging, depending on the particle size. The same problem occurs in many milling, micronization and tablet pressing applications. The preferred way to recover these sensitive and expensive products is with cyclone collectors due to their direct and sanitary powder capture. Unlike bag filters or wet scrubbers, cyclones minimize filter or product contamination and product cross ...
ByAdvanced Cyclone Systems, S. A. (ACS) based in Porto, PORTUGAL
ARM & HAMMER™ Sodium Bicarbonate is the trusted brand for formulation of healthcare products. Whether the application is as an active pharmaceutical ingredient or an excipient, manufacturers have come to rely on the consistent quality, regulatory compliance and technical support that come with the ARM & HAMMER™ brand. Explore the uses of sodium bicarbonate in pharmaceutical applications and dialysis by clicking on the links above or access product data using the menu to the ...
ByChurch & Dwight, Inc. based in Princeton, NEW JERSEY (USA)
Clinics and physicians rely on manufacturers to ensure drug efficacy of active pharmaceutical ingredients (APIs) and sterility assurance across the supply chain—for the health and safety of their patients. As a manufacturer, we understand that your choice of sterilization modality is unique. Enhancing the aseptic manufacture sterility assurance level (SAL) of pharmaceuticals without affecting drug efficacy is a critical requirement of terminal ...
BySterigenics U.S., LLC based in Oak Brook, ILLINOIS (USA)
The pharmaceutical industry is one of the most regulated industries. Contaminants in drug products are examined throughout the manufacturing process, since their presence affects drug stability, behaviour and toxicity. Therefore, regulatory bodies such as the European Medicines Agency (EMEA) and the American Food and Drug Administration (FDA) strictly enforce continuous and ongoing analysis of organic or inorganic impurities from raw materials, excipients and Active Pharmaceutical Ingredients (API) through ...
ByXenemetrix Ltd. based in Migdal Haemek, ISRAEL