Documentation has long been an important aspect of quality assurance roles across the pharmaceutical industry. While good documentation practices can be especially helpful during audits, inspections, and investigations, their utility doesn’t stop there. Documentation is a mandatory aspect of production at all levels to ensure that the products and processes of the facility remain up to standards. With quality assurance training from the Academy of Applied Pharmaceutical Sciences, you will have the opportunity to work in a state-of-the-art laboratory that simulates working in a GMP environment. By practicing what you’ll be doing in your career down the line, you can.. READ MORE »
Sanitized cannabis grow rooms are an integral aspect of any successful cannabis operation. With clean grow rooms, the quality and quantity of cannabis yield can be maximized, and growers can experience the reward of making the most of their crop. What’s more, safety hazards, diseases and invasive pests can all be prevented. As the industry expands and cannabis becomes more widely legalized, it’s becoming increasingly important for cultivators to define and adhere to good sanitation practices, while ensuring that their operation aligns with provincial and federal regulations. Within a grow room, a healthy environment for cultivation can be created by.. READ MORE »
Completing the Food Technology, Safety and Quality Diploma Program at AAPS will provide you with your food safety certification while experiencing a comprehensive yet practical, hands-on approach to learning the ins and outs of the industry. Whether you are just beginning your career or looking to complement and upgrade your existing knowledge and skills, our integrated approach will give you the confidence to develop, implement, and maintain food safety programs that comply with recognized standards. Hazard Analysis Critical Control Points (HACCP) is an internationally recognized food safety system focused on preventing, reducing, and eliminating biological, chemical, and physical hazards. It.. READ MORE »
A clear and well-documented clinical development plan (CDP) is the foundation of any good clinical study. In fact, it is a requirement for any pharmaceutical company that intends to develop and test a new drug. The CDP is a description of clinical trials that will be carried out on a drug to assess its safety and effectiveness. It covers everything from the reason for development to the features of the trial, timelines, costs, and other resources. Therefore, a good CDP must take into account regulations surrounding clinical trials, as well as good clinical practices. If you’re getting started in the.. READ MORE »
