Stainless Steel Literature Reviews Samples For Students

Introduction

Thin films are in use since ages, and in old times people used to beat gold with hammers into thin films about less than one μm thickness and then used this thin film for gold coating of different stuffs. Thin films are used in many materials and do use them in daily life but are not aware of it. If one wax cars or paint homes that mean, they are applying a thin film.

Bulk Material VS thin film

Bulk materials are those materials that are mined. They are referred to as Bulk solid in mining and mineral industry. The material that can be stored ...

The use of breath analysis to determine the state of a person’s health is a concept that dates back millennia (Gouma 26). Cardiovascular disease is an ailment for which current analysis methods involve invasive sampling. It has been suggested that the amount of cholesterol in blood can be measured by the amount of isoprene (Karl et al. 762) or carbon dioxide (Amann 34) in the breath.
One of the early methods to detect isoprene in breath is based on proton transfer reaction mass spectrometry (PTR-MS) (Karl et al. 762-763). In this technique, the breath sample is made to ...

Requirement for the Manufacture of Drugs concerning Public Safety

Abstract
The study will focus on pharmaceutical companies’ standard operation procedures. More in depth, the study will determine if cleaning validation and verification is a successful way to keep the quality of manufactured drugs at a high standard. The importance of the validation of a sterilization process will be examined. The study will list reasons for validation of sterilization through a set of regulatory expectations put in place by the FDA.
The regulatory expectations of the FDA will support the methods and analysis used to conduct this study. The study will also examine the success and failure of cleaning validation through ...

Introduction

Pharmaceutical companies should create and follow a standard operating procedure by implementing a cleaning validation to ensure future patient safety. Validation has received great attention by the FDA in recent inspections. Manufacturers must validate their cleaning process to ensure compliance with GMP regulations 1. One of the main keys in the manufacturing of dosage formulation is to develop cleaning procedures that will remove all types of residues from the equipment and containers. The goal of Cleaning Validation is to ensure effectiveness in cleaning equipment, and to prevent pollution and cross contamination of drug products to ensure the quality, safety; efficacy and ...