This new B.I. edition, two-fifths longer than its predecessor, continues to be a valued companion for the MBBS examinees, students in their clinical year and advanced nursing trainees. " Expanded for the first time with new chapters dealing with instruments used in Otolaryngology and Ophthalmology " Reflects changes taking place in contemporary medicine as additional material, while retaining all the features which have established a well earned reputation for the text. " Simple thumb-nail sketches of instruments, many of which have been redrawn and many added, improved legibility by the use of a different and slightly larger type-face and text description mostly in an interrogative form, are presented.
About the Book: This book has therefore subdivided the realm of medical instruments into the same sections like a text on physiology and introduces the basic early day methods well, before dealing with the details of present day instruments currently in
First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices practical knowledge about biomedical technology, regulations, and their relationship to quality health care.
Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new regulatory systems or refined the existing ones. A registered product requires a lot of technical documentation to prove its efficacy, safety, and quality. A smooth and successful registration process demands soft skills for dealing with various key stakeholders in the government, testing centers, and hospitals and among doctors. Handbook of Medical Device Regulatory Affairs in Asia covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. Government bodies, the medical device industry, and academics and students will find this book immensely useful in understanding the global regulatory environment and in their research and development projects.
Medical Instruments and Devices: Principles and Practices originates from the medical instruments and devices section of The Biomedical Engineering Handbook, Fourth Edition. Top experts in the field provide material that spans this wide field. The text examines how biopotential amplifiers help regulate the quality and content of measured signals. I
The Medical Device R&D Handbook presents a wealth of information for the hands-on design and building of medical devices. Detailed information on such diverse topics as catheter building, prototyping, materials, processes, regulatory issues, and much more are available in this convenient handbook for the first time. The Medical Device R&D Ha
This chapter focuses on adhesives used in direct physiological contact in dental and medical procedures. Activity in both areas has been quite extensive outside the United States for decades. In contrast, adhesive use in medical devices, patches, and plasters has been ongoing in the United States for a long time. In the case of medical devices, adhesion is concerned with the joining of materials such as plastics, elastomers, textiles, metals, and ceramics, which are examined in other chapters of the present volume and are covered in various references [1–6], The coverage of this chapter is devoted to applications where to adhesives are in direct contact with tissues and other live organs.
This handbook covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. It is the first to cover the medical device regulatory affairs in Asia. Experts from influential international regulatory bodies, including the US Food and Drug Administration (FDA), UK Medicines and Healthcare Products Regulatory Agency, Japan Pharmaceuticals and Medical Devices Agency, Saudi Food and Drug Authority, Korea Testing Laboratory, Taiwan FDA, World Health Organization, Asian Harmonization Working Party, Regulatory Affairs Professionals Society, and British Standards Institution, have contributed to the book. Government bodies, the medical device industry, academics, students, and general readers will find the book immensely useful for understanding the global regulatory environment and in their research and development projects.
Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new regulatory systems or refined the existing ones. A registered product requires a lot of technical documentation to prove its efficacy, safety, and quality. A smooth and successful registration process demands soft skills for dealing with various key stakeholders in the government, testing centers, and hospitals and among doctors. This handbook covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. It is the first to cover the medical device regulatory affairs in Asia. Each chapter provides substantial background materials relevant to the particular area to have a better understanding of regulatory affairs.
This 3rd Edition has been thoroughly revised and updated taking into account technological innovations and introduction of new and improved methods of medical diagnosis and treatment. Capturing recent developments and discussing new topics, the 3rd Edition includes a separate chapter on 'Telemedicine Technology', which shows how information and communication technologies have made significant contribution in better diagnosis and treatment of patients and management of health facilities. Alongside, there is coverage of new implantable devices as increasingly such devices are being preferred for treatment, particularly in neurological stimulation for pain management, epilepsy, bladder control, etc. The 3rd Edition also appropriately addresses 'Point of Care' equipment: as some technologies become easier to use and less expensive and equipment becomes more transportable, even complex technologies can diffuse out of hospitals and institutional settings into outpatient facilities and patient's homes. With expanded coverage, this exhaustive and comprehensive handbook would be useful forbiomedical physicists and engineers, students, doctors, physiotherapists, and manufacturers ofmedical instruments. Salient features: All chapters updated to address the current state of technology Separate chapter on 'Telemedicine Technology' Coverage of new implantable devices Discussion on 'Point of Care' equipment Distinctive visual impact of graphs and photographs of latest commercial equipment Updated list of references includes latest research material in the area Discussion on applications of developments in the following fields in biomedical equipment: micro-electronics micro-electromechanical systems advanced signal processing wireless communication new energy sources for portable and implantable devices Coverage of new topics, including: gamma knife cyber knife multislice CT scanner new sensors digital radiography PET scanner laser lithotripter peritoneal dialysis machine Describing the physiological basis and engineering principles of electro-medical equipment, Handbook of Biomedical Instrumentation also includes information on the principles of operation and the performance parameters of a wide range of instruments. Broadly, this comprehensive handbook covers: recording and monitoring instruments measurement and analysis techniques modern imaging systems therapeutic equipment
