Learn six sigma concept in industrial pharmacy. Explore definition, objectives, methodologies and application in pharmaceutical industry. Six sigma concept In Industrial pharmacy, Six Sigma define as a methodology which minimizes the defects and variations in pharmaceutical manufacturing. It aims for high-quality production by reducing errors and improving efficiency. The concept of Six Sigma initially was … Read more
Learn about quality by design in industrial pharmacy. Explore what are the objectives and advantages of QBD. Quality by design QBD is a systematic approach to pharmaceutical industry that are important for designing quality of a product. This concept developed by Dr. Joseph M. Juran, who believed that quality problems are related to which a … Read more
Learn total quality management definition, principle, advantages and disadvantages in industrial pharmacy. It is an element of quality management system. How to define total quality management (TQM)? Total Quality Management (TQM) is a management method which is used for improving the quality and productivity of business in an organization. It is a comprehensive management approach … Read more
Learn what is quality management system and certification with definition and what are the elements of quality management systems. QMS is an important aspect for the pharmaceutical industry for maintaining the quality and safety for their products and services. Quality Management System Quality Management System (QMS) is a set of policies, processes, documented procedures and … Read more
Learn about the Non-clinical drug development, goals and objectives. It is a process involving evaluation of safety and efficiency of drugs. What is Non-Clinical Drug Development? Non-clinical drug development or pre-clinical drug development is a risk process involving evaluation of safety and efficiency of drugs in animal drugs. Generally, pre-clinical studies are conducted to determine … Read more
Learn about Drug Development Teams and their roles, teamwork and the evolution of projects in this insightful guide. New drug development can be performed by various types of drug development organizations that may be private companies, not-for-profit organizations or private foundations. Some examples of private not-for-profit organizations include the Drugs for Neglected Diseases initiative (DNDi … Read more
Explore new drug approval process in India, it is crucial for pharmaceutical companies seeking to introduce new drugs to the Indian market. New Drug Approval Process in India In India, the Drug and Cosmetic Act of 1940 and Rules 1945 were announced by the Indian Parliament to regulate the import, manufacture, supply and sale of … Read more
Learn about regulatory requirements for drug approval worldwide. Here is the step-by-step process to bring new medicines to market. Regulatory Requirements for Drug Approval When it comes for approval of a new medicine, there are several rules to follow known as regulatory requirements for drug approval. Each country has its own unique regulatory requirements. This … Read more
Explore the key roles of Regulatory Affairs Department in Health Authorities and Pharmaceutical Industries. Discover their contributions to drug development, compliance, and global regulatory strategies. Roles of Regulatory Affairs Department Pharmaceutical Regulatory Affairs Departments have crucial role in the world of medicine. They help drug companies to follow rules and work with health agencies. This … Read more
Learn Drug regulatory authorities in pharmacy with list. Explore definition, list and key roles of these authorities. Each country has a regulatory agency that is accountable for imposing rules and regulations. It passes guidelines for drug development, registration, licensing, manufacturing, marketing and labelling of pharmaceutical products. Drug regulatory authorities Drug regulatory authorities define as organizations … Read more