Introduction (10%)
Explain the process of Direct Compression in tablet formulation including its advantages and disadvantages in comparison with alternative methods. This section should be around 150-200 words in length.
Aim (5%)
State the aim of your work. This section should be around 25-50 words in length.
Methods (20%)
Include the specific details of the formulation, the methodology used in blending and/or granulation, the manufacturing process and pharmacopoeial testing procedures used. This section should be around 250-300 words in length.
Results (10%)
Include a table summarising your tablet testing results (do not include raw data values)
Discussion (40%)
Detail here the relevance of the results you obtained. Do not rewrite them in words but discuss their pharmaceutical importance and significance. You should…
Explain the choice of excipients in your formulation
Explain the results obtained between the two batches
Do your results comply with pharmacopoeia standards? Provide an explanation.
What further tests could have been performed and what information would have been obtained from these tests?
Conclusions (10%)
A concise summary of the key points from your report
References (5%)
Include full details of any reference sources which have been cited in the report (Lecture notes are not a suitable reference source)
