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can you Explain in 1000 words, the Methods and standards for disposal of biomedical waste
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- The first photo is the procedure while the other photo is the problem that needs to be answered. Please answer correctly, and provide proper solutions. Thank youuuuD, Inc., uses three departments to produce a detergent. The Finishing Department is the third and last step before the product is transferred to storage. All materials needed to give the detergent its final composition are added at the beginning of the process in the Finishing Department. The company uses FIFO costing. The following data for the Finishing Department for October have been made available: Production data: In process, October 1 (labor and factory overhead, 75% complete) 10,000 litres Transferred in from preceding department 40,000 litres Finished and transferred to storage 35,000 litres In process, October 31 (labor and factory overhead, 50% complete)15,000 litres Additional data: Work-in-process inventory, October 1: Cost from preceding department $38,000Cost from this department: 21,500 Materials 39,000 Labor 42,000 Factory overhead $140,500 Transferred in during October $140,500Cost added in this department: Materials $70,000Labor 162,500Factory…What are the possible lab hazards that may occur during the processing and manufacturing of drugs in industry?
- you are asked to develop a risk management plan for laboratories working with biohazards. describe the risk assessment analyses that you would undertake in developing your plan.3) Define gel electrophoresis, including its theory and application. Describe the steps of running gel electrophoresis using the following image. More detailed reading: https://www.sciencedirect.com/topics/medicine-and-dentistry/agar-gel-electrophoresis POWER SUPPLY CATHODE ELECTROPHORETIC BUFFER ANODE WELL SAMPLE AGAROSE GEL POWER SUPPLY CATHODE ANOCE HIGH MOLECULAR WEIGHT SPECIES LOW MOLECULAR WEIGHT ANALYTESA) What is an effective method you can used to ensure the accuracy of laboratory results?
- Briefly define the role of cGMP for the quality control unit in the pharmaceutical industry ? Please answer at your own easy words.I would like to ask for the introduction of the laboratory exercise about MICROBIOLOGY: Microscopic Morphology of Microbes. In would include the principles, significance of the study, objectives of the experiment, and how the objectives were achieved. This part must also be in the passive voice and past tense. The introduction must be short but packed with relevant contentEach of the following statements describes the role of the Pharmacy Technician in the preparation of radiopharmaceuticals EXCEPT: Select one: O a. O b. O C. O d. Ability to perform calculations of both Curie and SI units of radioactivity Perform precalibration and postcalibration activities Transcribe and generate computer labels Determine the required doses for each patient according to patient's weight
- What are the purposes of a pharmaceutical packaging? Please answer at your own words.In sterilization, which among the supplies, instruments, glassware, etc. under the list of materials can be sterilized using either or both equipment below? List them down. For "autoclaving" For Dry heat oven Can be sterilized only sterilization with either Materials: 200-ml Erlenmeyer flask Stove 500-ml Erlenmeyer flask Autoclave 10-ml graduated cylinder Analytical balance 100-ml graduated cylinder pH meter Spatula Stirring rod 100-ml beaker Test tubes Distilled water Petri dish Stirring rod Alcohol lamp Glass dropperMICROBIOLOGY: Microscopic Morphology of Microbes Write your introduction (This includes principles, significance of the study, objectives of the experiment and how the objectives were achieved, methodology and redults and discussions. This part must also be in the passive voice and past tense. Introduction must be short but packed with relevant content). Just answer results and discussions and objectives.
