The challenges to pharma companies from COVID- and how they continue to respond was a topic raised at the FDA/Xavier PharmaLink conference, which was held March -, . Challenges discussed included uninterrupted supply of medicines, risk management plans, relationships with regulators, and animal trials.
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Daily Unique Visitors: | 1,018 |
Daily Pageviews: | 2,036 |
Income Per Day: | $ 6.00 |
Estimated Worth: | $ 1,440.00 |
Google Indexed Pages: | Not Applicable |
Yahoo Indexed Pages: | Not Applicable |
Bing Indexed Pages: | Not Applicable |
Google Backlinks: | Not Applicable |
Bing Backlinks: | Not Applicable |
Alexa BackLinks: | Not Applicable |
Google Safe Browsing: | No Risk Issues |
Siteadvisor Rating: | Not Applicable |
WOT Trustworthiness: | Very Poor |
WOT Privacy: | Very Poor |
WOT Child Safety: | Very Poor |
Alexa Rank: | 861,621 |
PageSpeed Score: | 72 ON 100 |
Domain Authority: | 49 ON 100 |
Bounce Rate: | Not Applicable |
Time On Site: | Not Applicable |
Total Traffic: | No Data |
Direct Traffic: | No Data |
Referral Traffic: | No Data |
Search Traffic: | No Data |
Social Traffic: | No Data |
Mail Traffic: | No Data |
Display Traffic: | No Data |
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Jan 31, 2018 · We took a snapshot of the 4 warning letters the FDA sent to medical device companies last quarter. Device manufacturing violations ranged from failing to evaluate...
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Jul 05, 2018 · As the keeper of the world’s largest database of FDA 483s, we often get asked, “How do you get a hold of actual 483 reports and who else can see them?” This is...
FDA 483s Resource Center Resources to Avoid & Respond to FDA 483s Form FDA 483s. If you're part of the very small fraternity of people who have "FDA 483s" in your vocabulary,...
Nov 30, 2020 · 1. Manufacturers and importers must submit reports when they become aware of information that reasonably suggests that one of their marketed devices may have...
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FDA's Centers of Excellence in Regulatory Science and Innovation (CERSIs) are collaborations between FDA and academic institutions to advance regulatory science through...
Sep 26, 2019 · FDA is expanding its New Inspection Protocol Project (NIPP) inspection methodology, initially piloted exclusively for sterile drug manufacturing facilities, to...
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Oct 03, 2019 · FDAzilla is a data analytics and inspection documents provider. This company provides a variety of tools that make data more usable, searchable, and actionable.
H1 Headings: | Not Applicable | H2 Headings: | 5 |
H3 Headings: | 12 | H4 Headings: | 3 |
H5 Headings: | Not Applicable | H6 Headings: | Not Applicable |
Total IFRAMEs: | Not Applicable | Total Images: | 32 |
Google Adsense: | Not Applicable | Google Analytics: | UA-19780785-1 |
Words | Occurrences | Density | Possible Spam |
---|---|---|---|
LEARN MORE | 8 | 0.693 % | No |
tool for | 6 | 0.52 % | No |
READ MORE | 6 | 0.52 % | No |
Barbara W | 6 | 0.52 % | No |
essential tool | 6 | 0.52 % | No |
W Unger | 6 | 0.52 % | No |
and quality | 4 | 0.347 % | No |
is an | 4 | 0.347 % | No |
quality professionals | 4 | 0.347 % | No |
at the | 4 | 0.347 % | No |
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supply chain | 4 | 0.347 % | No |
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FDAzilla is | 4 | 0.347 % | No |
issues and | 4 | 0.347 % | No |
Unger March | 4 | 0.347 % | No |
the data | 4 | 0.347 % | No |
to help | 4 | 0.347 % | No |
that may | 4 | 0.347 % | No |
Words | Occurrences | Density | Possible Spam |
---|---|---|---|
Barbara W Unger March | 4 | 0.347 % | No |
MORE The essential tool | 4 | 0.347 % | No |
The essential tool for | 4 | 0.347 % | No |
COVID19 Challenges Collaboration with | 3 | 0.26 % | No |
to COVID19 Challenges Collaboration | 3 | 0.26 % | No |
Challenges Collaboration with Regulators | 3 | 0.26 % | No |
Collaboration with Regulators is | 3 | 0.26 % | No |
is Essential Going Forward | 3 | 0.26 % | No |
Regulators is Essential Going | 3 | 0.26 % | No |
with Regulators is Essential | 3 | 0.26 % | No |
Response to COVID19 Challenges | 3 | 0.26 % | No |
Patients First in Response | 3 | 0.26 % | No |
MHRA GMP Inspection Deficiencies | 3 | 0.26 % | No |
GMP Inspection Deficiencies for | 3 | 0.26 % | No |
Inspection Deficiencies for 2018 | 3 | 0.26 % | No |
2 MHRA GMP Inspection | 3 | 0.26 % | No |
Part 2 MHRA GMP | 3 | 0.26 % | No |
Puts Patients First in | 3 | 0.26 % | No |
Pharma Puts Patients First | 3 | 0.26 % | No |
Big Pharma Puts Patients | 3 | 0.26 % | No |
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Domain Registrar: | NameCheap, Inc. |
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Registration Date: | 2009-12-30 1 decade 4 years 10 months ago |
Last Modified: | 2019-12-04 4 years 11 months 2 weeks ago |
Host | IP Address | Country | |
---|---|---|---|
kia.ns.cloudflare.com | 173.245.58.179 | United States | |
wesley.ns.cloudflare.com | 108.162.193.246 | United States |
Host | Type | TTL | Extra |
---|---|---|---|
fdazilla.com | A | 212 |
IP: 104.27.155.37 |
fdazilla.com | A | 212 |
IP: 104.27.154.37 |
fdazilla.com | NS | 86400 |
Target: wesley.ns.cloudflare.com |
fdazilla.com | NS | 86400 |
Target: kia.ns.cloudflare.com |
fdazilla.com | SOA | 3600 |
MNAME: kia.ns.cloudflare.com RNAME: dns.cloudflare.com Serial: 2033561681 Refresh: 10000 Retry: 2400 Expire: 604800 |
fdazilla.com | MX | 300 |
Priority: 1 Target: aspmx.l.google.com |
fdazilla.com | MX | 300 |
Priority: 10 Target: aspmx2.googlemail.com |
fdazilla.com | MX | 300 |
Priority: 10 Target: aspmx3.googlemail.com |
fdazilla.com | MX | 300 |
Priority: 30 Target: aspmx4.googlemail.com |
fdazilla.com | MX | 300 |
Priority: 30 Target: aspmx5.googlemail.com |
fdazilla.com | MX | 300 |
Priority: 5 Target: alt1.aspmx.l.google.com |
fdazilla.com | MX | 300 |
Priority: 5 Target: alt2.aspmx.l.google.com |
fdazilla.com | TXT | 300 |
TXT: ca3-08223d26201e4ec6b08acdfbb9a57654 |
fdazilla.com | TXT | 300 |
TXT: google-site-verification=dUNSf2DfeBC74Bh yQCWTCyaAKC1vlAyK-IGAfCxo-Qw |
fdazilla.com | TXT | 300 |
TXT: MS=ms79579480 |
fdazilla.com | TXT | 300 |
TXT: fdazilla-com.azurewebsites.net |
fdazilla.com | TXT | 300 |
TXT: google-site-verification=cc8qPkTUtyD-w1C wi4QjG7VXvJnZQiBs_KLZQ954z1Y |
fdazilla.com | AAAA | 213 |
IPV6: 2606:4700:3035::681b:9a25 |
fdazilla.com | AAAA | 213 |
IPV6: 2606:4700:3037::681b:9b25 |
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