Medical Safety Services For Medical Management
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PremiumManufactured by Advanced Energy Industries, Inc.based in USA
Shorten product development, increase reliability, and benefit from compliance expertise. Increased lifestyle conditions, patient lifespans, and outpatient procedures are transforming medical equipment. Equipment needs to be more mobile, include data storage and insight capabilities, and be more precise than ever. These requirements drive innovation and make shortened product development cycles ...
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Manufactured by Alfa Chemistrybased in USA
One of the most important steps in the process of developing a medicine is determining its safety. Alfa Chemistry is dedicated to providing pre-clinical drug research services to support our clients' drug development, pre-clinical and clinical investigations, and assist them in deciding which drug candidates are most worthwhile to pursue in clinical trials. We emphasize pharmacology, ...
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based in INDIA
To govern radiation safety in operation of medical diagnostics in India, Atomic Energy Regulatory Board) Issued guidelines in December 2012: All medical diagnostic radiation equipment should be registered and submit QA report once in every two years. Our AERB Trained professionals provide all support required related to medical radiation equipment and safety needs to achieve As Low As ...
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by STEMartbased in USA
CE marking is the manufacturer's declaration that their product complies technically and administratively with the essential regulatory requirements of Medical Device Directive 93/42/EEC (MDD) and its supplementary Directive 2007/47/EEC, Active Implantable Medical Devices Directive 90/385/EEC (AIMDD) and In Vitro Diagnostics Directive (IVDD) 98/79/EC, which outline the safety and performance ...
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Manufactured by Dagri Inzeniring D.O.O.based in SLOVENIA
Safety tests and inspection of any medical equipment. Regular yearly examination of medical equipment. Safety examinations of medical equipment. Calibration of medical equipment. Validation of medical equipment. The making of the final report and enclosing the certificate of validated ...
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Manufactured by Avaniabased in AUSTRALIA
Avania clinical safety management specializes in the distillation and dissemination of the information you need to design an efficient program and bring your product to ...
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Manufactured by CD Formulationbased in USA
Water vapor transmission capacity refers to the amount of water vapor through the specimen in a certain period of time under the specified temperature, relative humidity, and certain water vapor pressure. The main role of the drug bottle is to protect the safety of drugs in the process of storage and transportation, to ensure the stability of the validity period. Water vapor transmission amount ...
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Manufactured by Bausch + Lomb GmbHbased in GERMANY
A key to success of Storz Ophthalmic Instruments has been its ability to maintain hand-crafted excellence, while adapting to an ever changing surgical environment with the latest instrument ...
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Manufactured by Ivenix, Inc.based in USA
Managing the business of infusion safety. More than 90% of hospitalized patients receive IV therapy.1 Adverse IV drug events are commonplace, costing the average facility more than 6 million annually.2-5 The infusion process is complex with many moving parts. Yet, today infusion outcomes, efficiency and patient satisfaction are more important than ever before, not only for patient care. but also ...
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Manufactured by Omnicellbased in USA
Connective pharmacy automation technology to unleash full potential. Healthcare leaders and clinicians need pharmacy technology that simplifies operations instead of complicating them. This is achieved when your systems are integrated and interoperable. Omnicell solutions connect the pharmacy ecosystem by surfacing real-time data insights, streamlining pharmacy business, and enabling new ...
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Manufactured by Omnicellbased in USA
Optimize clinician workflow and patient care, at every point. Omnicell’s Point of Care clinical workflow technology optimizes medication management, patient care, and pharmacy performance so clinicians can spend more time focused on ...
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by 4cRiskbased in AUSTRALIA
4cRisk provides onsite emergency medical care services to clients located both nationally and ...
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based in GERMANY
We use medical devices in our laboratories. Therefore we are subject to the Medical Devices Act and the Medical Device Operator Ordinance. Paragraph 6 of the currently valid Medical Device Operator Ordinance requires us to appoint a representative for medical device ...
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Manufactured by Omnicellbased in USA
Your partner for optimized outcomes. Through industry-leading packaging and automation solutions, Omnicell® Medication Adherence empowers pharmacies to work more efficiently, to improve medication safety and satisfaction for their employees, customers and ...
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based in USA
After years of successful clinical research, submission of documents for Health Authority (HA) review requires a specialized skill of clear and precise clinical report writing. Such clear and precise clinical writing aids reviewers to easily comprehend the technicalities of clinical research, as a single error in clinical documentation may prove risky and costly for organizations, causing delays ...
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by HingeClinicabased in USA
Our Medical and scientific Writing team is an integral part of clinical research. Our Medical Writers closely associate with biostatistics, medical affairs, safety and data management teams to deliver accurate, timely, and cost effective deliverables to the highest quality and scientific standards. We have a wide breadth of experience drawn from the pharmaceutical industry and clinical research ...
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Manufactured by BYTEC Medizintechnik GmbHbased in GERMANY
We advise you fully in all matters relating to your medical device - regulatory, technical and economical - during all stages of the product life cycle. ...
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based in GERMANY
When it comes to medical devices, quality and safety are especially vital. As a notified body, we can help you with your conformity assessment procedure and ensure that your active and non-active medical devices comply with EU Directive 93/42/EEC. Tap into the European ...
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Manufactured by Egemen Internationalbased in TURKEY
PMS (Post Marketing Surveillance) activities consist of a process in which the performance and safety of medical devices are continuously monitored after the supply of products to the market. The necessity for post-market monitoring of a medical device begins immediately after the medical device is placed on the ...
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