If you can confirm or contradict a position for your own region, please date the answer. An undated regional claim is the least useful thing in this category.
Posted with less confidence than the sentence structure implies.
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1.
If you can confirm or contradict a position for your own region, please date the answer. An undated regional claim is the least useful thing in this category.
Posted with less confidence than the sentence structure implies.
The failure mode on prescription requirements and telehealth models is boring rather than dramatic. It is almost always the step everyone assumes was done correctly because it is too simple to get wrong.
Post #61 answers the question as asked. The question underneath it is different.
I would call the community position on prescription requirements and telehealth models likely rather than established, and I would be comfortable defending that hedge.
Worth separating two things that post #61 runs together.
Generic or biosimilar entry depends on patent and exclusivity positions that are jurisdiction-specific and are frequently misreported.
This is the sort of thing the wiki should carry and currently does not.
Summarising the prescription requirements and telehealth models thread so far, since it is long and the answer is buried: the first reply has the method, the fourth has the correction to it, and the rest is people agreeing at length.
Picking up post #69: that is the part I would want checked first.
Agreed on prescription requirements and telehealth models, with one qualification that I think matters. The reasoning holds for the case as described. Change the starting assumption and it does not, and the starting assumption is the part nobody states.
Practical experience of prescription requirements and telehealth models, offered as one case with the conditions stated, not as a general finding. Conditions first, because they are what make it interpretable.
Where a claim about legality is made here, the useful follow-up is which instrument it rests on. Most such claims turn out to rest on a forum post.
I would be glad to be shown a cleaner way of putting this.
Post #71 is right about the mechanism and I think understates the practical bit.
A definition problem is doing most of the work in this prescription requirements and telehealth models discussion. Once the term is pinned down I suspect the disagreement mostly goes away and what is left is small.
Coming back to post #70, because the follow-up matters more than the original answer.
Nothing in this subcategory is legal advice, and the members who work in regulated environments are the most careful to say so.
What I would check first on prescription requirements and telehealth models is whether the thing being measured moved or whether the way of measuring it moved. Those look identical in a graph.
Nothing to add, except that this is the answer I would give if asked.
My understanding of prescription requirements and telehealth models is a few years old and may have been superseded. If it has been, I would genuinely like to know rather than keep repeating it.
Generic or biosimilar entry depends on patent and exclusivity positions that are jurisdiction-specific and are frequently misreported.
Where a claim about legality is made here, the useful follow-up is which instrument it rests on. Most such claims turn out to rest on a forum post.
Before the thread moves on from prescription requirements and telehealth models — what is the sample size behind the claim? I am not being difficult; I have seen the same figure quoted from an n of four and from an n of four hundred.
Everything in post #80 holds. The case it does not cover is the one I have.
Two things can be true about prescription requirements and telehealth models at once: the mechanism is plausible and the evidence for the size of the effect is thin. Most of the argument here is people defending the first against attacks on the second.
Post #83 put the caveat in the right place and I want to underline it.
For anyone finding this later: the short answer on prescription requirements and telehealth models is that it depends on one thing, and the rest of the thread is people identifying which thing.
An indication approved for one age range does not extend to another, and paediatric extensions are separate decisions with separate evidence.
Practical note on prescription requirements and telehealth models: write down what you expect before you look. The number of times I have found what I went looking for is higher than chance would allow.
Where I part company with post #87, and it is a narrow parting.
Answering the prescription requirements and telehealth models question as asked, then the question I think is meant. As asked: yes, with the qualification below. As meant: it depends on how the first measurement was taken.