Practical Gas Chromatography
Title
Word limit is 1500 (excluding results table and reference list).
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)
Description
Just in case here are all the files needed for the report.
