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GMP Compliance Efficiencies (1-Page)
Describe why regulatory authorities inspect a pharmaceutical manufacturer against pertinent GMPs. Compare and contrast specific GMPs for the manufacture of for example drug substance versus finished product (e.g. ICH Q7 versus 21 CFR Part 211). Summarise the GMPs requirement for ‘Validation'.
1.1 Key Enablers for a QMS (1-Page)
Describe the business drivers for a QMS and the key enablers to make a QMS successful. Briefly describe a ‘Product Realisation' strategy that aligns design activities against specification activities.
1.2 Cost Effective Validation (1-Page)
Describe an efficient approach to ‘Validation' driven by subject matter expertise and risk based decision making.
Why a substance is being heated at a fast rate the temperature of decomposition
Assist with the setting of design variables necessary for sizing equipment
Use Laplace transformation to solve the initial value problem
Equal rates of mass transfer for the production of the fine chemical are required. This is often required for certain types of organic synthesis.
Application of reverse osmosis principles for the desalination of sea water
Prepare the design and evaluation of a new chemical manufacturing process.
Adsorption and Membrane Processes
Draw T-S diagram of the cycle.
The potential energy between two atoms A and B are constants and r the interatomic separation distance.
Implications of the future of fabrication for international trade, transportation, and logistics
The atmospheric pressure of 100k Pa acts on the other side of the piston. The gas is heated until the volume is doubled and the final pressure is 500 kPa. Calculate the work done by the gas.
Evaluate particle diameter at different terminal gas velocities
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