Executive Development Programme in Drug Preservation Methods
-- ViewingNowThe Executive Development Programme in Drug Preservation Methods is a comprehensive certificate course, designed to equip learners with critical skills in drug preservation. This program underscores the importance of maintaining the efficacy and safety of drugs during storage and distribution, a vital aspect of the pharmaceutical industry.
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⢠Fundamentals of Drug Preservation: An introduction to the basic principles of drug preservation, including the factors affecting drug stability and the importance of proper storage conditions.
⢠Pharmaceutical Packaging: An examination of the different types of packaging materials used in drug preservation and their properties, as well as the principles of package design and evaluation.
⢠Temperature Control and Management: A focus on the role of temperature in drug preservation, including the recommended storage temperatures for different drug products, and the use of temperature monitoring and control systems.
⢠Humidity Control: An exploration of the impact of humidity on drug stability, and the methods and technologies used to control humidity in drug storage areas.
⢠Light Exposure Protection: A discussion of the effects of light on drug stability and the importance of protecting drugs from excessive light exposure during storage, including the use of opaque packaging and light-resistant storage areas.
⢠Microbial Contamination Prevention: An examination of the risks associated with microbial contamination of drugs, and the measures used to prevent contamination, including the use of aseptic techniques, sterilization, and sanitation.
⢠Transportation and Distribution of Drugs: A focus on the challenges associated with transporting and distributing drugs, and the measures used to ensure drug stability during transportation, including the use of temperature-controlled shipping and handling practices.
⢠Quality Assurance and Control in Drug Preservation: An exploration of the role of quality assurance and control in drug preservation, including the development and implementation of quality standards, the use of quality control testing and monitoring, and the management of deviations and non-conformities.
⢠Regulations and Guidelines for Drug Preservation: A review of the regulatory requirements and guidelines governing drug preservation, including the guidelines issued by international organizations such as the World Health Organization (WHO) and the Food and Drug Administration (FDA).
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