Hi AD,
Some great points there. I have been thinking along the same lines. [Hence my date of April 4th] I worked for many years in Local Govt in a compliance role, the last several years in Planning and Building where we would often ask for for amendments relating to Planning and Building applications. Sometimes requesting an amendment that could take a while as it involved fundamental changes and required starting from scratch again, and other times simply requesting more information. That application is put aside awaiting that information. The way I understand it the FDA have asked for the later. Information on MPL in animals, I see this as extra information to support the information already supplied. I struggle to accept the people responsible would put it on the bottom of the pile and start again, that makes no sense. Better to put it aside and move it on as soon as you get that info.
Hope that makes sense.
Either way MPL is well on the way to a result.
Happy Friday
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