Pharmaceutical Industry Insights
Technical articles on excipients, capsules, GMP and GSP standards and pharmaceutical regulation, written by Larissa Pharma's team of pharmacists.
- Documentation & regulatory7 min read
The quality documentation a material purchase should come with
CoA, MSDS, CO, CQ, GMP certificate and DMF each answer a different question. What production needs, what the registration dossier needs, and what a GMP inspection will ask for.
Read article - Standards & regulation7 min read
GSP in Vietnam under Circular 36/2018/TT-BYT
Good Storage Practice in Vietnam now follows Circular 36/2018/TT-BYT, not the 2001 decision. Who must comply, what is required, and how to verify a supplier's GSP status.
Read article - Excipients8 min read
What excipients are, and how to choose them
Excipients have no pharmacological action, yet they decide whether a tablet compresses, disintegrates on time and stays stable to expiry. The seven functional classes and how to choose by dosage form.
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Formulation questions rarely fit an article
These articles set out general principles. A specific formulation problem — an incompatibility, a stability issue, choosing between pharmacopoeial grades — is faster to resolve directly with our pharmacists.