regulatory.ie

REGULATORY AFFAIRS

Regulatory Affairs by Kara Daly. Challenges in developing NIR methods for release testing, assay andor uniformity of content. October 17th, 2012. Currently the US Pharmacopeia monograph requires content uniformity tests to be performed on solid-dosage form samples at a frequency of 10 per batch. The FDA asserts that quality cannot be tested into products, it should be built in or should be by design. 1 US FDA Guidance for Industry PAT- A Framework for Innovative Pharmaceutical. October 17th, 2012.
traffic

OVERVIEW

The website regulatory.ie presently has an average traffic classification of zero (the lower the more traffic). We have downloaded twenty pages inside the web site regulatory.ie and found zero websites associating themselves with regulatory.ie.
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20

REGULATORY.IE TRAFFIC

The website regulatory.ie is seeing fluctuating levels of traffic through the year.
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LINKS TO REGULATORY.IE

WHAT DOES REGULATORY.IE LOOK LIKE?

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REGULATORY.IE SERVER

I revealed that a single root page on regulatory.ie took one thousand two hundred and fifty milliseconds to come up. I could not detect a SSL certificate, so therefore our crawlers consider this site not secure.
Load time
1.25 sec
SSL
NOT SECURE
IP
81.17.254.88

SERVER SOFTWARE AND ENCODING

We diagnosed that regulatory.ie is utilizing the Apache/2.0.52 (Red Hat) os.

SITE TITLE

REGULATORY AFFAIRS

DESCRIPTION

Regulatory Affairs by Kara Daly. Challenges in developing NIR methods for release testing, assay andor uniformity of content. October 17th, 2012. Currently the US Pharmacopeia monograph requires content uniformity tests to be performed on solid-dosage form samples at a frequency of 10 per batch. The FDA asserts that quality cannot be tested into products, it should be built in or should be by design. 1 US FDA Guidance for Industry PAT- A Framework for Innovative Pharmaceutical. October 17th, 2012.

PARSED CONTENT

The website has the following in the web page, "Challenges in developing NIR methods for release testing, assay andor uniformity of content." I viewed that the web site also stated " Currently the US Pharmacopeia monograph requires content uniformity tests to be performed on solid-dosage form samples at a frequency of 10 per batch." They also said " The FDA asserts that quality cannot be tested into products, it should be built in or should be by design. 1 US FDA Guidance for Industry PAT- A Framework for Innovative Pharmaceutical."

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