Population-scale and rapid testing for SARS-CoV-2 continues to be a priority for several parts of the world. We revisit the in vitro technology platforms for COVID-19 testing and diagnostics—molecular tests and rapid antigen tests, serology or antibody tests, and tests for the management of COVID-19 patients. Within each category of tests, we review the commercialized testing platforms, their analyzing systems, specimen collection protocols, testing methodologies, supply chain logistics, and rel...

Allergy & Clinical Immunology  Electrochemistry  Information Technologies  Medical Education  Biological Chemistry  Virology  Medicinal Chemistry  Developmental Biology  Environmental Sciences  Biological Engineering  Genomics  Genetics  Food Science & Technology  Marketing  Oncology  Technology And Innovation  Theoretical Chemistry  Diagnostics  Supply Chain Management  Biological Materials  Nanometer Materials  Drugs & Devices  Public Health  Organic Chemistry  Epidemiology  Sales Management  Molecular Biology  Health Policy  Microbiology  Global Health  Bioengineering  Physical Chemistry  Bioinformatics  Biotechnology  Functional Materials  Computational Biology  Cell Biology  Parasitology  Translational Medicine  Infectious Diseases  Women’s Health  Immunology  Respiratory Medicine  Materials Engineering  Internal Medicine  Metabolic Sciences  Medical Genetics 

Doi:10.3390/s21196581

The workplace influences the safety, health, and productivity of workers at multiple levels. To protect and promote total worker health, smart hardware, and software tools have emerged for the identification, elimination, substitution, and control of occupational hazards. Wearable devices enable constant monitoring of individual workers and the environment, whereas connected worker solutions provide contextual information and decision support. Here, the recent trends in commercial workplace tech...

Information Technologies  Public Economics  Behavioral Economics  Automata  Computer and Network Security  Agricultural Engineering  Communication Protocols  Environmental Sciences  Environmental Sciences  Cloud Computing  Innovation Management  Artificial Intelligence  Big Data Search and Mining  Business Management  Information Management  Applications of Communication Systems  Chemical Engineering & Technology  Food Science & Technology  Marketing  Machine Learning  Diagnostics  Electric Engineering  Civil Engineering  Computer Engineering  Aquaculture, Fisheries & Fish Science  Information retrieval  Mechanical Engineering  Bioengineering  Mineral Engineering  Bioinformatics  Information and Communication: Security, Privacy, and Trust  Biophysics  Information and communication theory and algorithms  Distributed computing  Physical Education  Grid Computing  Business Communication  Consumer Behavior  Corporate Governance  Distance and Open Education  Engineering Management  Entrepreneurship  Software Engineering  Applied Physics  Opsearch  Information Science  Public Policy  E-Learning and Knowledge Management  Economics  Technology  Demography  Mobile and Portable Communications Systems  Mobile and Ubiquitous Networks  Mobile Computing Systems  Multimedia/Signal processing  Business Ethics and Corporate Social Responsibility  Socioeconomics  Business Finance and Investment  Business Analysis  Economic System  Business and Economics Education  Electronic Commerce  Information Economics  Advertising  Total Quality Management  Supply Chain Management  Drugs & Devices  Public Health  Sports Science  Sales Management  Marine Biology  Statistics  Risk Management  Project Management and Strategy  Dynamical System  Project Management  Public Administration  Materials Engineering 

Doi:10.1002/aisy.202100099

Due to the lack of sound approval process for medical devices in the EU people are suffered from many side effects. Some of the case studies which reflected mainly for the transformation of medical device regulations are PIP implants, MOM hip implants, COSTAR drug-eluting stent, and pleural seal, etc. To reflect the progress over the last 20 years, the EU revised the legal framework. Regulation (EU) 2017/745 on medical devices (MDR) introduces a major update of the regulatory framework in the Eu...

Drugs & Devices 

Doi:10.22270/ijdra.v8i3.394

The present article summarizes & simplify the marketing application requirements i.e. the critical aspects of marketing application in different CTD using countries, Process to prepare and review the requirements for CMC section (Chemistry manufacturing & Control) for filing an application in regulated market. Study shows the compilation of dossier as per CTD format with minimum errors during filing. The focus is on the application filing & Query part that may come after submission & during ...

Drugs & Devices 

Doi:10.22270/ijdra.v5i2.196

“Why didn’t they develop natural product drugs in a sustainable manner at the beginning of this century?” In 2035, when about 10.0 billion will inhabit Earth, will this be our legacy as the world contemplates the costs and availability of synthetic and gene-based products for primary health care? Acknowledging the recent history of the relationship between humankind and the Earth, it is essential that the health care issues being left for our descendants be considered in terms of resources. Fo...

Drugs & Devices  Biotechnology  Microbiology  Biochemistry  Biodiversity  Metabolic Sciences