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Compliance Handbook for Pharmaceuticals, Medical Devices, and Biologics

This text lists the necessary steps for meeting compliance requirements during the drug development process. It presents comprehensive;

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Compliance Handbook for Pharmaceuticals, Medical Devices, and Biologics

This text lists the necessary steps for meeting compliance requirements during the drug development process. It presents comprehensive;

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Guide to Microbiological Control in Pharmaceuticals and Medical Devices

, and principles of sterilization, including microbiological-specific considerations for biotechnological products and other medical devices. It;

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Haschek and Rousseaux's Handbook of Toxicologic Pathology

pathology for scientists and researchers studying and making decisions on drugs, biologics, medical devices and other chemicals, including;

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Medical Device Quality Assurance and Regulatory Compliance

Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents;

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Medical Device Quality Assurance and Regulatory Compliance

Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents;

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Managing Medical Devices within a Regulatory Framework

) best practices for medical records management, interoperability between and among devices outside of healthcare, and the dynamics;

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Rational Therapeutics for Infants and Children

development and proper use of drugs, biologics, and medical devices for infants and children. It explores the scientific underpinnings and clinical;

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Drug-Drug Interactions for Therapeutic Biologics

in drug response of the co-administered drugs. Using illustrative case studies and examples, Drug-Drug Interactions for Therapeutic Biologics;

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Bioprocess Engineering

For Senior-level and graduate courses in Biochemical Engineering, and for programs in Agricultural and Biological Engineering or;

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International Labeling Requirements for Medical Devices, Medical Equipment and Diagnostic Products

. Coverage includes requirements such as text, dimensions, type sizes, graphic elements, symbols, and language for implantable devices, sterile;

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International Labeling Requirements for Medical Devices, Medical Equipment and Diagnostic Products

. Coverage includes requirements such as text, dimensions, type sizes, graphic elements, symbols, and language for implantable devices, sterile;

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Applications of Polymers and Plastics in Medical Devices

materials for medical devices, covering fundamentals, materials, applications and regulatory requirements. Sections cover the role of plastics;

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Medical Device Regulatory Practices

practical examples and case studies. Medical devices, like pharmaceuticals, are highly regulated, and the bar is raised constantly as patients and;

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Medical Regulatory Affairs

countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. Experts from;

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Medical Device Quality Management Systems

Medical Devices Quality Management Systems: Strategy and Techniques for Improving Efficiency and Effectiveness is written for the needs;

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Hydrophilic Polymer Coatings for Medical Devices

and devices. It concisely provides both the scientific basics of this class of polymers and the up-to-date information needed for product;

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Hydrophilic Polymer Coatings for Medical Devices

and devices. It concisely provides both the scientific basics of this class of polymers and the up-to-date information needed for product;

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Economics Of Medical Technology

Medical technology broadly defined to include all aspects of the process of treating disease (e.g., pharmaceuticals, medical devices, and;

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Sources of Contamination in Medicinal Products and Medical Devices

The first one-volume guide to sources of contamination in pharmaceuticals and medical devices Most books dealing with contaminants;

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Do No Harm - Protecting Connected Medical Devices, Healthcare, and Data from Hackers and Adversarial Nation States

increasing expansion of medical devices and the dark side of the high demand for medical devices The medical device regulatory landscape and the;

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Sterilization Validation and Routine Operation Handbook (2001)

The validation and radiation sterilization process for biomaterials and medical devices requires careful planning to ensure regulatory;

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Assurance of Sterility for Sensitive Combination Products and Materials

Assurance of Sterility for Sensitive Combination Products and Materials: New Paradigms for the Next Generation of Medical Devices and;

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Plastics in Medical Devices

, marketing and commercialization of medical devices and materials for use in medical devices ;

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Handbook of Medical Device Design

First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices;

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Handbook of Medical Device Design

First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices;

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Medical Devices and Human Engineering

biomedical engineering. Medical Devices and Human Engineering, the second volume of the handbook, presents material from respected scientists with;

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