Medical Management Training
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Analytik Jena - Web Seminar From Sample to Result
Molecular biology methods can be used in a wide variety of applications. To ensure that you get the maximum quality in your results, proper planning of the workflow and experimental set up is vital. This online seminar provides an overview of the steps needed to be taken in setting up a molecular biology lab routine. The individual steps will be expanded upon in the other installments of Analytik ...
By Analytik Jena - an EndressHauser Company based in Jena, GERMANY. from Web Seminars for Pharma & Life Science Training line
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IVD Directive to IVD Regulation Transition Training Course
There are significant changes in the European legislation applicable to IVDs. The IVD Regulation has replaced the IVD Directive, which will impose new requirements on manufacturers and other economic operators. By attending this course, you’ll discover the new requirements and how these will affect your organization. ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - CE Marking Training Training line
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Analytik Jena - Web Seminar: A Role for Biofoundries in Rapid Development and Validation of Automated SARS-CoV-2 Clinical Diagnostics
The SARS-CoV-2 pandemic has shown how a rapid rise in demand for patient and community sample testing can quickly overwhelm testing capability globally. With most diagnostic infrastructure dependent on specialized instruments, their exclusive reagent supplies quickly become bottlenecks, creating an urgent need for approaches to boost testing capacity. Prof. Paul Freemont and colleagues at the ...
By Analytik Jena - an EndressHauser Company based in Jena, GERMANY. from Web Seminars Chemical Analysis & Life Science Training line
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Incident and Accident Investigations Training Courses
This training establishes techniques an investigator can use to collect information relating to an investigation in a comprehensive and objective manner, and utilize that information to develop corrective actions validated by a root-cause analysis method. This training is for supervisors and individuals that are responsible for investigating or processing workplace incidents of any ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Hospital Staff Injury Prevention Training line
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IAIA Virtual Symposium
Our Interconnected World: Impact Assessment, Health, and the ...
By International Association for Impact Assessment (IAIA) based in Fargo, NORTH DAKOTA (USA).
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ISO 14971 Medical Devices Risk Management Training Courses
This course is designed to provide participants with an understanding of the impact that ISO 14971 has on the decision making process at medical device manufacturing firms. This one-day training course helps medical device professionals gain an understanding of how ISO 14971 can improve their business and risk management efforts. Participants will also understand how ISO 14971 applies to ISO ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - Specialist Training Training line
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Requirements of the In Vitro Diagnostic Regulation Training Course
The In Vitro Diagnostic Regulation details the requirements which manufacturers have to meet to sell In Vitro Diagnostic devices in the European Union. It replaces the In Vitro Diagnostic Directive. This course introduces you to the key requirements of the IVDR. IVDs will now be classified according to their risk using a new rule-based system. The majority of IVDs will be subjected to independent ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - CE Marking Training Training line
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BSI - ISO 45001 Occupational Health and Safety Management
Embed a culture of health and safety with the new global ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA).
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Implementing ISO 13485:2016 - Training Courses
You'll be introduced to the concepts needed to understand, develop and implement a Quality Management System (QMS). This course provides the knowledge and process steps to enable the effective implementation of a QMS that is in line with the requirements for ISO 13485:2016 ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - ISO 13485 Training Training line
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Analytik Jena - Web Seminar Optimized Workflow
Hepatitis virus infections concern people all over the world. According to estimates by the World Health Organisation (WHO, 2019), 71 million people are chronically infected with HCV. In 2016, the WHO published a Global Health Sector Strategy for the elimination of viral hepatitis. One important pillar of the program is to make treatment and diagnostics accessible and affordable for people in ...
By Analytik Jena - an EndressHauser Company based in Jena, GERMANY. from Web Seminars Chemical Analysis & Life Science Training line
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Office Ergonomics Awareness Training
Do you work in an office setting? If so, this training provides you with the knowledge of injury factors in the office environment, and how to apply ergonomic principles to reduce your risk for ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Hospital Staff Injury Prevention Training line
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BSI - ISO 13485 Quality Management System Software
Medical device manufacturing is one of the most regulated sectors in which significant quality systems and product requirements must be satisfied. The regulatory requirements are intended to ensure that manufacturers consistently design, produce and place onto the market medical devices that are safe and fit for their intended purpose. The ISO 13485 standard is an effective solution to meet the ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA).
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Cytiva - Microbiology Membrane Filtration for Water Quality Testing Webinar
Microbiological quality has the potential for immediate impact to the consumer and public health. Whether for determining the safety for human contact, use, and consumption or detecting organisms that cause spoilage and reduced shelf life, a reliable membrane filter is one of the most important testing elements. In this webinar learn about the history of membranes and how to select the right ...
By Cytiva based in Marlborough, MASSACHUSETTS (USA).
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Radiation Safety Officer Review
This course is designed for active RSOs who have previously taken a 40-hour class to keep up on the constant changes in Radiation Protection Standards. Based on NUREG 1556, this fast-paced class gives an in-depth review of the principles of radiation safety including dose limits, required ALARA programs, record keeping, compliance, and training plant personnel. We recommend attending a review ...
By VEGA Americas, Inc. based in Cincinnati, OHIO (USA).
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ISO 13485:2016 Senior Management Briefing Training Courses
As a leader, your commitment and support is crucial to the success of your organization's ISO 13485:2016 Medical Devices Quality Management System (QMS). This interactive briefing has been designed around the requirements of the standard and highlights your responsibilities in terms of leadership and commitment. The focus is on helping senior management migrate their system from ISO 13485:2003 to ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - ISO 13485 Training Training line
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Analytik Jena - Web Seminar Find the Right Way to Prep
Thoughtful experimental set-up and correct sample preparation is vital to get the most out of a given sample. Whether you are seeking to analyze your specimens at the protein or the nucleic acid level, it is always important to keep some key points in ...
By Analytik Jena - an EndressHauser Company based in Jena, GERMANY. from Web Seminars for Pharma & Life Science Training line
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ISO 13485:2016 Transition Training Courses
Are you already familiar with ISO 13485:2003/EN 13485:2012 and want to find out about ISO 13485:2016? This comprehensive course introduces you to the new requirements and explores the changes between ISO 13485:2003/EN 13485:2012 and the latest standard. With greater attention on the organization's ability to meet applicable customer and regulatory requirements, ISO 13485:2016 focuses on the ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - ISO 13485 Training Training line
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Understanding ISO 14971:2007 Training Courses
BSI's "Understanding ISO 14971:2007" course is designed to provide participantswithan understanding of the impact that ISO 14971:2007 has on the decision making process at medical device manufacturing firms. This one-day training course helps medical device professionals gain an understanding of how ISO 14971:2007 can improve their business and risk management efforts. Participants will also ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - Specialist Training Training line
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Performance Evaluation and Clinical Evidence for IVDs Training Course
If you are involved in planning, conducting or documenting performance evaluation and clinical performance studies for IVD devices in Europe, this intensive one day course will enable a greater understanding of performance evaluation for In Vitro Diagnostic devices under the IVD Regulation, how performance fits into the product development lifecycle and IVD Regulation (IVDR) requirements for ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - Specialist Training Training line
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Medical Device Directive CE Marking
BSI's “Medical Devices CE Marking” three day course is designed to provide participants with the knowledge to assist their companies in getting products to market more quickly. Management personnel responsible for all aspects of CE marking medical devices as well as internal and external auditors will benefit from this course. Participants will gain knowledge of the requirements of ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - CE Marking Training Training line
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