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home about us about panacea meet the team careers services pharmacovigilance regulatory affairs veterinary pharmacovigilance medical device vigilance clinical trials services quality management & auditing news all news panacea news industry news #panaceainsights contact us privacy notice home about us about panacea meet the team careers services pharmacovigilance regulatory affairs veterinary pharmacovigilance medical device vigilance clinical trials services quality management & auditing news all news panacea news industry news #panaceainsights contact us privacy notice pharmaceutical support services at panacea we believe in a better way of doing things. everyone talks about delivering a fresh, dynamic, approach – but at panacea you will find that we deliver on this promise. our highly experienced team enjoy working with clients to find the best way to safeguard their investment and reputation, and we take pride in providing the best possible vigilance and regulatory affairs services to the pharmaceutical industry. currently, panacea are responsible for marketing authorisation’s in every eu country and have an international reputation which is respected by regulators. pharmaceutical support services at panacea we believe in a better way of doing things. everyone talks about delivering a fresh, dynamic, approach – but at panacea you will find that we deliver on this promise. our highly experienced team enjoy working with clients to find the best way to safeguard their investment and reputation, and we take pride in providing the best possible vigilance and regulatory affairs services to the pharmaceutical industry. currently, panacea are responsible for marketing authorisation’s in every eu country and have an international reputation which is respected by regulators. areas of expertise pharmacovigilance panacea offers end-to-end pharmacovigilance solutions for products at the pre, peri and post-marketing stages of their lifecycle more information medical device vigilance we monitor the safety profile of medical devices, from the processing and reporting of single adverse incidents through to the removal of products from the market as part of a field safety corrective action more information veterinary vigilance the science connected to the monitoring, assessment, detection, understanding and prevention of unrecognised adverse effects or changes in the patterns of adverse effects of veterinary medicines more information quality management & auditing our audit function has experience on both sides of the pharmacovigilance audit table. we help our clients with inspection readiness, post-inspection assistance, and routine pharmacovigilance audits. more information clinical trials services panacea holds an established approach to supporting companies, helping to effectively contribute new and improved products to the market in the most efficient manner, and with as little resources as allowable more information regulatory affairs from initial concept to ma authorisation, our regulatory team can assist with your initial regulatory strategy, dossier compilation and ectd publishing needs. we operate a 'right-first-time' approach, always. more information our approach we are flexible and responsive, whether it’s a one-off task, a fixed term project (large or small) or a continuous relationship over several years. we know that each client is different; each has a specific budget, timescale, and objective, and we do everything we can to work with them to ensure that budget targets are met, timescales respected, and objectives achieved. individually, everyone at panacea takes personal responsibility for providing the highest quality of work. collectively, we offer a responsive, cost effective, flexible, and professional service. about us our approach we are flexible and responsive, whether it’s a one-off task, a fixed term project (large or small) or a continuous relationship over several years. we know that each client is different; each has a specific budget, timescale, and objective, and we do everything we can to work with them to ensure that budget targets are met, timescales respected, and objectives achieved. individually, everyone at panacea takes personal responsibility for providing the highest quality of work. collectively, we offer a responsive, cost effective, flexible, and professional service. about us what our clients say the field of post-marketing pharmacovigilance is very different in europe, largely due to the legislation, and we had the option of bringing someone into the business to set-up our own internal post-marketing service, or working together with a company who could provide pharmacovigilance support in the post-marketing phase. we decided to go with panacea pharma projects because we felt that they really understood our needs and requirements. european generics company we’ve been very impressed by the way ppp took such a structured approach to reviewing the requirements of the new pharmacovigilance legislation, and to implementing them on our behalf in such a professional and timely way. eu licence holder the wealth of experience and expertise in ppp’s team provides us with reassurance that we are in good hands. german ma holder panacea has provided training to our safety and pharmacovigilance department on the new pharmacovigilance legislation that came into effect in 2012, and how it will affect our daily safety activities. this is typical of the willingness and ability of panacea to offer a bespoke service that is tailored to our unique business needs. our link with panacea has allowed us to bid on projects that previously we would have had to decline. each proposal is different in terms of the scope of services required, but throughout all of them panacea has provided us with excellent post-marketing pharmacovigilance support. european generics company our latest news panacea’s christmas jumper day effort – for save the children ema – new gvp chapter iv on specific considerations for the paediatric population the panacea team present cheques to four local charities panacea’s #medsafetyweek update panacea at global generics awards 2018 back at work in a brexit world – clarisse ceotto pharmacovigilance agreements (pva’s) – five key aspects that should be included. evdas and the new pharmacovigilance signal management requirements the benefit: risk balance – proactive pharmacovigilance the pharmacovigilance risk management plan more news our immersive corporate video click here to watch locate us peterson house middle river douglas isle of man im2 1al contact us [email protected] phone: +44 1624 672 777 fax: +44 1624 678 877 follow us privacy policy | © 2018 all rights reserved | website by openjumbo.com 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. visit our privacy notice for full details. accept cookie statement

URL analysis for panaceapharmaprojects.com

http://www.panaceapharmaprojects.com/panacea-news/pharmacovigilance-agreements-pvas-five-key-aspects-that-should-be-included/
http://www.panaceapharmaprojects.com/panacea-news/back-at-work-in-a-brexit-world-by-clarisse-ceotto/
http://www.panaceapharmaprojects.com/contact-us/
http://www.panaceapharmaprojects.com/cookie-policy/
http://www.panaceapharmaprojects.com/panacea-news/the-panacea-team-present-cheques-to-four-local-charities/
http://www.panaceapharmaprojects.com/services/
http://www.panaceapharmaprojects.com/news-blog-all/news-blog-panacea-news/
http://www.panaceapharmaprojects.com/about-us/meet-the-team/
http://www.panaceapharmaprojects.com/news-blog-all/
http://www.panaceapharmaprojects.com/news-blog-all/news-blog-industry-news/
http://www.panaceapharmaprojects.com/news-blog
http://www.panaceapharmaprojects.com/panaceainsights/evdas-and-the-new-pharmacovigilance-signal-management-requirements/
http://www.panaceapharmaprojects.com/about-us/
http://www.panaceapharmaprojects.com/news-blog-all/news-blog-panaceainsights/
http://www.panaceapharmaprojects.com/panacea-news/panaceas-medsafetyweek-update/

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;

Domain Name: PANACEAPHARMAPROJECTS.COM
Registry Domain ID: 1615953888_DOMAIN_COM-VRSN
Registrar WHOIS Server: whois.1and1.com
Registrar URL: http://registrar.1and1.info
Updated Date: 2018-03-17T12:15:10Z
Creation Date: 2010-09-15T22:27:21Z
Registry Expiry Date: 2018-09-15T22:27:21Z
Registrar: 1&1 Internet SE
Registrar IANA ID: 83
Registrar Abuse Contact Email: [email protected]
Registrar Abuse Contact Phone: +1.6105601459
Domain Status: clientTransferProhibited https://icann.org/epp#clientTransferProhibited
Name Server: NS1051.UI-DNS.BIZ
Name Server: NS1051.UI-DNS.COM
Name Server: NS1051.UI-DNS.DE
Name Server: NS1051.UI-DNS.ORG
DNSSEC: unsigned
URL of the ICANN Whois Inaccuracy Complaint Form: https://www.icann.org/wicf/
>>> Last update of whois database: 2018-04-16T15:17:35Z <<<

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

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currently set to expire. This date does not necessarily reflect the expiration
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registrar. Users may consult the sponsoring registrar's Whois database to
view the registrar's reported date of expiration for this registration.

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

  REGISTRAR 1&1 Internet SE

SERVERS

  SERVER com.whois-servers.net

  ARGS domain =panaceapharmaprojects.com

  PORT 43

  TYPE domain

DOMAIN

  NAME panaceapharmaprojects.com

  CHANGED 2018-03-17

  CREATED 2010-09-15

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

NSERVER

  NS1051.UI-DNS.BIZ 217.160.81.51

  NS1051.UI-DNS.COM 217.160.82.51

  NS1051.UI-DNS.DE 217.160.80.51

  NS1051.UI-DNS.ORG 217.160.83.51

  REGISTERED yes

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