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home global europe pan-european regulatory bodies national agencies uk goverment bodies public assessment reports european organisations usa japan other africa asia australia and new zealand canada central and south america middle east glossaries contact menu reg-info.com is a collection of regulatory information sources providing links to websites with information relating to regulatory affairs and the regulation and development of medicines. in preparing regulatory strategy, including for regulatory submissions, it is essential to know where to find key regulatory guidance and regulatory intelligence sources to facilitate regulatory learning. european medicines agency european commission european national regulatory agencies fda – cder fda – cber japanese mhlw ich tim felgate news updates from the ema and fda below are updates from ema's and fda's news feeds , showing some of the most recent items published. these feeds provide links to information on the ema's and fda's websites. recent ema updates agenda: agenda - prac draft agenda of meeting 11-14 june 2018 11th june 2018 human medicines european public assessment report (epar): abraxane, paclitaxel, revision: 21, authorised 11th june 2018 pharmacovigilance risk assessment committee (prac): 11-14 june 2018, european medicines agency, london, uk, from: 11-jun-2018, to: 14-jun-2018 11th june 2018 agenda: agenda - hmpc agenda of the 4-5 june 2018 meeting 11th june 2018 committee for herbal medicinal products (hmpc): 4-5 june 2018, european medicines agency, london, uk, from: 04-jun-2018, to: 05-jun-2018 11th june 2018 human medicines european public assessment report (epar): signifor, pasireotide, revision: 11, authorised 11th june 2018 human medicines european public assessment report (epar): atryn, antithrombin alfa, revision: 14, authorised 11th june 2018 outcome of written procedures during the period 22 february 2018 to 21 may 2018 11th june 2018 management board meeting dates 2019 – 2021 11th june 2018 report: summary of transfers of appropriations in budget 2018 11th june 2018 human medicines european public assessment report (epar): mixtard, insulin human (rdna), revision: 17, authorised 11th june 2018 management board meeting: 6-7 june 2018, european medicines agency, london, uk, from: 06-jun-2018, to: 07-jun-2018 11th june 2018 recent updates from the fda federal judge enters consent decree against delta pharma 8th june 2018 #dyk opioids are among the type of medication that are most commonly misused - https://go.usa.gov/xq7az #fdainnovationchallengepic.twitter.com/kqpmn4ezxd 8th june 2018 (@fdadeviceinfo) statement from fda commissioner scott gottlieb, m.d., on 2017 national youth tobacco survey results and ongoing fda efforts to protect youth from the dangers of nicotine and tobacco products 7th june 2018 #fda announces draft guidance: “requests for feedback and meetings for #medicaldevice submissions: the q-submission program”. comment period closes in 60 days https://go.usa.gov/xqsce 7th june 2018 (@fdadeviceinfo) fda seeks permanent injunction against company selling unapproved hand sanitizers that claim to prevent infections from numerous pathogens 6th june 2018 manufacturers assistance and technical training branch (mattb) 6th june 2018 happy #nationaleyewearday https://go.usa.gov/xqa4m pic.twitter.com/t4rjyqrdyn 6th june 2018 (@fdadeviceinfo) fda deputy commissioner for policy, planning, legislation, and analysis anna abram, remarks prepared for testimony before a subcommittee of the u.s. house committee on energy and commerce on the pandemic and all-hazards preparedness act 6th june 2018 #dyk the misuse of prescription drugs means taking a medication in a manner or dose other than prescribed; taking someone else’s prescription, even if for a legitimate medical complaint such as pain; or taking a medication to feel euphoria. #fdainnovationchallengepic.twitter.com/qi0mrjactv 5th june 2018 (@fdadeviceinfo) fda and usda announce key step to advance collaborative efforts to streamline produce safety requirements for farmers 5th june 2018 fda takes action against 53 websites marketing unapproved opioids as part of a comprehensive effort to target illegal online sales 5th june 2018 fda warns companies to stop selling dangerous and illegal pure and highly concentrated caffeine products 5th june 2018 although care has been taken in compiling the information on this website, the author cannot be held responsible for the accuracy of the information, nor for any consequences arising from its use. you are advised to seek additional advice when making decisions based on the information you have obtained through this website. the regulatory intelligence blog wrapping up draft definitions of regulatory intelligence ri tips: how to add an mhra search engine to google chrome yahoo to discontinue pipes service ri tips - cleaning up messy data from regulatory agencies are you missing the old mhra web site? (updated) searching the eu regulatory agencies copyright © 1997 - 2018. tim felgate. all rights reserved. we use cookies to ensure that we give you the best experience on our website. if you continue to use this site we will assume that you are happy with it. accept

URL analysis for reg-info.com

https://www.reg-info.com/other/africa/
https://www.reg-info.com/other/central-and-south-america/
https://www.reg-info.com/europe/european-regulatory-bodies/
https://www.reg-info.com/
https://www.reg-info.com/contact-us/
https://www.reg-info.com/other/canada/
https://www.reg-info.com/other/middle-east/
https://www.reg-info.com/usa/
https://www.reg-info.com/other/asia/
https://www.reg-info.com/other/australia-and-new-zealand/
https://www.reg-info.com/other/glossaries/
https://www.reg-info.com/europe/
https://www.reg-info.com/europe/european-organisations/
https://www.reg-info.com/japan/
https://www.reg-info.com/europe/european-national-agencies/uk-goverment-bodies/

Whois Information

Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;

Whois Server Version 2.0

Domain names in the .com and .net domains can now be registered
with many different competing registrars. Go to http://www.internic.net
for detailed information.

Domain Name: REG-INFO.COM
Registrar: TUCOWS DOMAINS INC.
Sponsoring Registrar IANA ID: 69
Whois Server: whois.tucows.com
Referral URL: http://www.tucowsdomains.com
Name Server: NS1.UK26.SITEGROUND.EU
Name Server: NS2.UK26.SITEGROUND.EU
Status: clientTransferProhibited https://icann.org/epp#clientTransferProhibited
Status: clientUpdateProhibited https://icann.org/epp#clientUpdateProhibited
Updated Date: 07-apr-2017
Creation Date: 26-jan-2004
Expiration Date: 26-jan-2018

>>> Last update of whois database: Sat, 08 Jul 2017 17:41:54 GMT <<<

For more information on Whois status codes, please visit https://icann.org/epp

NOTICE: The expiration date displayed in this record is the date the
registrar's sponsorship of the domain name registration in the registry is
currently set to expire. This date does not necessarily reflect the expiration
date of the domain name registrant's agreement with the sponsoring
registrar. Users may consult the sponsoring registrar's Whois database to
view the registrar's reported date of expiration for this registration.

TERMS OF USE: You are not authorized to access or query our Whois
database through the use of electronic processes that are high-volume and
automated except as reasonably necessary to register domain names or
modify existing registrations; the Data in VeriSign Global Registry
Services' ("VeriSign") Whois database is provided by VeriSign for
information purposes only, and to assist persons in obtaining information
about or related to a domain name registration record. VeriSign does not
guarantee its accuracy. By submitting a Whois query, you agree to abide
by the following terms of use: You agree that you may use this Data only
for lawful purposes and that under no circumstances will you use this Data
to: (1) allow, enable, or otherwise support the transmission of mass
unsolicited, commercial advertising or solicitations via e-mail, telephone,
or facsimile; or (2) enable high volume, automated, electronic processes
that apply to VeriSign (or its computer systems). The compilation,
repackaging, dissemination or other use of this Data is expressly
prohibited without the prior written consent of VeriSign. You agree not to
use electronic processes that are automated and high-volume to access or
query the Whois database except as reasonably necessary to register
domain names or modify existing registrations. VeriSign reserves the right
to restrict your access to the Whois database in its sole discretion to ensure
operational stability. VeriSign may restrict or terminate your access to the
Whois database for failure to abide by these terms of use. VeriSign
reserves the right to modify these terms at any time.

The Registry database contains ONLY .COM, .NET, .EDU domains and
Registrars.

  REGISTRAR TUCOWS DOMAINS INC.

  REFERRER http://www.tucowsdomains.com

SERVERS

  SERVER com.whois-servers.net

  ARGS domain =reg-info.com

  PORT 43

  SERVER whois.tucows.com

  ARGS reg-info.com

  PORT 43

  TYPE domain

DOMAIN

  NAME reg-info.com

NSERVER

  NS1.UK26.SITEGROUND.EU 77.104.132.65

  NS2.UK26.SITEGROUND.EU 77.104.171.61

STATUS
clientTransferProhibited https://icann.org/epp#clientTransferProhibited
clientUpdateProhibited https://icann.org/epp#clientUpdateProhibited

  CHANGED 2017-04-07

  CREATED 2004-01-26

  EXPIRES 2018-01-26

  REGISTERED yes

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