drug-administration Downloads
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Our FRONT-LINE™ series of field sterilizers are U.S. Food and Drug Administration (FDA) cleared. This steam sterilizer brings advanced steam sterilization technology and a new surgical capability closer to the point of injury in any austere environment. ...
ACAM2000, (Smallpox (Vaccinia) Vaccine, Live) is a live, vaccinia virus smallpox vaccine licensed in the U.S. by the Food and Drug Administration for active immunization against smallpox disease for persons determined to be at high risk for smallpox infection. ...
Polydextrose is a synthetic polymer of glucose. It is a food ingredient classified as soluble fibre by the U.S. Food and Drug Administration (FDA) as well as Health Canada, as of April 2013. It is frequently used to increase the non-dietary fibre content of food, to replace sugar, and to reduce calories and fat content. It is a multi-purpose food ingredient synthesized from dextrose (glucose), ...
Hydrophilic injection filter for protection against particle and bacterial contamination of small amounts of drugs during administration; Compatible with all Luer-Lock connectors; Filter diameter 25 mm; Filter area 4.0 cm²; Low priming volume. ...
Made of transparent plastic, aseptic, with an innovative design and removable parts, it makes the work of doctors and nurses faster and easier. ...
Hydrophilic injection filter for protection against particle and bacterial contamination of small amounts of drugs during administration; Different connectors are available; Filter area 2.3 cm²; Filter diameter 18 mm; Compatible with all Luer-Lock connectors; Low priming volume. ...
As new information and science become available, this system is, and will continue to be, updated and improved. • The U.S. Food and Drug Administration (FDA) ensures the safety, effectiveness, and availability of vaccines for the United States. ...
CELLENE™ MC1053 is a high clarity, nontoxic, halogen and phthalate free, flexible thermoplastic elastomer compound developed specifically for extrusion applications in the food and medical industries. All components used in the manufacturing of CELLENE™ MC1053 are sanctioned by the US Food & Drug Administration for food applications under Title 21 of the Code of Federal ...
Oral TPOXX® (tecovirimat) is the first drug approved by the U.S. Food and Drug Administration (FDA) that is specifically indicated for the treatment of smallpox disease in adults and pediatric patients weighing at least 13 kg. (Prescription Label) TPOXX® inhibits viral maturation of variola virus (the virus that causes smallpox) and other poxviruses by preventing the formation of a ...
Medication Delivery The MAD Nasal Device from Teleflex was invented by an emergency physician and offers a useful, additional option in the choice of alternate access for medication delivery.* Rapidly Effective Nasal drug administration with the MAD Nasal Device is quick and easy, eliminating IV set-up time and conserving resources. Additionally, no sterile technique is required, so more time is ...
PK/PD and non-compartmental analyses can be time consuming, requiring detailed attention to every step from data preparation to report generation. Phoenix WinNonlin™’s integrated tools for data processing, graphing & charting, report generation, and compliance create an efficient, all-in-one collaboration workbench. Phoenix WinNonlin is used by over 10,000 scientists at more than ...
ByCertara
Especially designed for mice, rats, guinea-pig and rabbits, our perfusion systems are used in pharmacological research and Toxicology, to investigate liver, kidney or mesenteric beds vascular activity and physiology, in response to drug challenges. The system provides heated, oxygenated, and nutrient-rich perfusate to the organ with or without drug administration and electrical ...
The BIRMINGHAM HIP◊ Resurfacing (BHR◊) System is a conservative approach to hip arthroplasty in which an all-metal bearing couple is used to preserve, rather than replace, a patient’s femoral head and neck. It was first implanted in July 1997, and was approved for use in the United States by the Food and Drug Administration in 2006. Since its introduction, there have been over ...
Pharmaceutical Grade Micro-Media® Series Depth Filter Media is manufactured in accordance with ErtelAlsop Drug Master File located at the United States Food and Drug Administration Center for Drug Evaluation and Research.CompositionErtelAlsop Micro-Media® filter sheets are composed of cellulose pulp, Diatomaceous Earth and/or ...
The iPRECIO programmable pump is an advanced infusion device for drug delivery applications in mice, rats and larger animals. With versatile programmable functions and a refillable reservoir, this implantable infusion pump enables full control over dosing studies and empowers researchers to execute even the most complex dosing protocols, including multiple bolus dosing, variable/constant ...
More than 57 million doses have been distributed to date, and there have been no serious safety concerns.Vaccine safety continues to be monitored by CDC and the Food and Drug Administration (FDA). These studies continue to show that HPV vaccines are safe. ...
TÜV Rheinland can help you to navigate these require-ments and understand established methods of both manufacturing control and quality in compliance with Japanese Good Manufacturing Practice (GMP).FDA Third Party Services As an Accredited Person (AP) TÜV Rheinland is authorized by the U.S. Food and Drug Administration (FDA) to perform Third Party Reviews and ...