Kira oversees EMMA International’s corporate planning efforts. In addition to overseeing day-to-day operations at ...
All pharmaceuticals and medical devices are manufactured in clean rooms which have certain levels of cleanliness ...
Most of the common medical devices that are utilized multiple times throughout their lifespan, must be properly ...
Nanotechnologies in medical devices, drugs, and cosmetics are on the rise and becoming more prevalent [1,2]. ...
The American Society for Testing and Materials (ASTM) is an organization that publishes production and testing ...
The Food and Drug Administration (FDA) utilizes regulatory standards developed by non-governmental organizations ...
Good Manufacturing Practices (GMP) is a system that consists of processes, procedures and documentation that ...
Good Manufacturing Practices (GMP) is a system that consists of processes, procedures and documentation that ...
The voluntary eSTAR (electronic Submission Template And Resource) is a fillable portable document format (PDF) ...
Medical device reporting (MDR) is one of the post market surveillance tools used by the FDA to monitor medical ...
With the growth of computational capabilities, artificial intelligence (AI) and machine learning (ML) have become ...
In 1906 the Pure Food and Drug Act (Dr. Wiley’s Law) was passed by the Congress and signed by President Theodore ...