kronin
Joined 12 years ago
Joined 12 years ago
I am at a medium sized company. We acquired a startup. They did not "live and die with automation", instead they contracted out the production operations. A dozen customers, all on snowflake systems which were constantly tweaked directly in prod with no documentation or audit process.
My experience on the acquirer side is that startup engineers like to just build stuff and deploy it. Design? Testing? Documentation? Automation? None of that existed in this company in any fashion. And they are themselves grating against a modicum of process. Please explain what you want to do, why, and provide a high level design. You are going to replace the whole auth system, it's not something you just "figure out" as you go along... Sigh.
That's assuming a single multi-tenant saas footprint.
There is absolutely nothing preventing you from standing up a footprint in each compliance region and customers are assigned to the region that satisfies their requirements for data location.
You get the benefit of less footprints to manage, while still meeting the requirements necessary to serve your customers.
And if you have a customer that absolutely must have isolated infrastructure, stand one up for them and pass along the increased cost associated.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369496/
Strange that the study would focus on individuals who received a 250-μg dose. The adult dose is 100-μg (https://reference.medscape.com/drug/mrna-1273-moderna-covid-...). Yes, the study states that key findings were validated with 8 participants who received the regular dosage, but still seems odd to me.
The comparison dataset is explained as: "The convalescent plasma samples were characterized in earlier studies (13–16) and grouped into an early time point of 15 to 60 days after symptom onset and a late time point of 100 to 150 days after symptom onset."
So the comparison was between vaccinated individuals, most of whom received a higher dose than is being given out, to infected individuals, and the time periods don't exactly line up. For the vaccinated dataset, the time periods were 7 and 90 days after the second dose. For the other dataset, the time periods were 15-60 days, and 100-150 days after symptom offset.
Deeper into the study, there is also this: "The escape maps of the 100-μg cohort resembled those of the 250-μg cohort and fell into the 456/484-targeting, core-targeting, or flat categories (fig. S6). Although the sample sizes are small, and a higher fraction of the 100-μg dose escape maps were flat than for the 250-μg cohort (4 of 8 versus 5 of 14, respectively), this suggests that 100- and 250-μg doses elicit antibody responses similar in the breadth of their RBD-binding specificity."
Java 11 is the newest LTS release. The next LTS release will be Java 17. Many companies won't touch anything that isn't LTS. There are still a large number of companies staying on Java 8 :shrug:
I've tried to use electronic whiteboard alternatives and it's just not as fluid when trying to get ideas out. Maybe an iPad Pro with a Pencil, but I haven't sprung for one of those yet...
[1] https://www.pegasusav.us/pegasus-magnetic-glass-marker-board...
We then use this in a typescript generator to generate client code.
Instead, build your artifact and publish it to an artifact repository, just like we used to.
_then_ wrap that artifact in a Docker image.
Vulnerability found in the docker image? No problem. Build a new image with the same artifact.