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in gmp peptide synthesis, there are a lot to consider:

Synthesis strategy (i.e. solid phase peptide synthesis, solution phase peptide synthesis)
• Protection groups (i.e. Boc-, Fmoc - processes)
• Purification strategy (i.e. preparative HPLC, conventional chromatography, ion exchange, gel chromatography, counter-current distribution)
• Flexibility and upscaling
• Special customer request (i.e. dedicated production lines)
• Special equipment (i.e. enzymatic unit, electrolysis unit)
For finished dosage forms intended for clinical trials or commercial supply, CreativePep offers for its Active Pharmaceutical Ingredients (APIs)
• Formulation development
• Compatibility studies
• Sterile filling in cooperation with partners
• Release
• Stability studies

I got this info from the website of Creative Peptides (creative-peptides.com). Hope it's useful for you.

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Q: What should be taken into consideration in gmp peptide synthesis?
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