Two things before anyone answers the substance.
First, the context in the first post is clear and specific. Second, the question is framed so that an answer can actually address it. Both are the norm here and both matter more than they sound.
Two things before anyone answers the substance.
First, the context in the first post is clear and specific. Second, the question is framed so that an answer can actually address it. Both are the norm here and both matter more than they sound.
Research-use-only status is a legal classification, not a safety classification. It means the compound is sold for laboratory use and not for human consumption. The label does not establish whether the molecule is safe, efficacious, or toxic.
Compounding and pharmacy rules: some jurisdictions allow a pharmacy to compound a drug that is not on the market under specific conditions. The conditions are strict and vary by jurisdiction. Generalising from one country's rules to another's is unreliable.
I disagree with the reply above, and I think the disagreement is substantive rather than terminological.
The distinction being drawn does not survive when you look at the published data for this specific question. I would be glad to be shown wrong on this, because the version I am arguing against is more convenient.
Worth separating two things that post #70 runs together.
Import restrictions vary by compound and by jurisdiction: what is a controlled substance in one place is legal to purchase in another. What you can import for personal use depends on your country's rules, not on where it is sold.
This follows post #90 rather than contradicting it.
For anyone arriving from a search: the marked solution above is the direct answer, and the replies underneath it add the caveats that make it safe to use.
Read the full topic (98 posts)
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Follow-up: How compounding permissions changed when supply normalised
How compounding permissions changed when supply normalised I have a specific reason for asking rather than idle curiosity, and the context is below. Structured report rather than an opinion, following the…
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+72 | 77 | 1.5k | 1d |
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Reading a regulatory notice rather than an article about it — what changed since
Reading a regulatory notice rather than an article about it — what changed since — setting out what I have, and where I think it stops being reliable. A logistics question, since the answers here are usually…
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+28 | 32 | 640 | 13mo |
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Pharmaceutical compounding rules, summarised from primary sources — a second dataset
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+50 | 56 | 780 | 8mo |
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Enforcement priorities versus written rules
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2 | 62k | 15mo | |
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Second pass at: Import rules for personal quantities, by jurisdiction, dated
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2 | 5k | 11mo |
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Import rules for personal quantities, by jurisdiction, dated
On the subject in the title: Import rules for personal quantities, by jurisdiction, dated Working notes rather than a conclusion. Structured report rather than an opinion, following the format the maintainers…
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3 | 60k | 12mo | |
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Coming back to: When "no data" is the complete and final answer
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+77 | 82 | 12k | 11mo |
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Manufacturer assistance programmes and their eligibility rules
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+37 | 42 | 32k | 11d |
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Managing an unplanned gap in supply
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+105 | 110 | 5.1k | 3mo |
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Cost per milligram, computed honestly across formats — the long version
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+111 | 124 | 24k | 14mo |