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Title | Horn Pharmaceutical Consulting - ASMF, Active Substance Master File, US-DMF, Drug Master File, |
Description | HORN Pharmaceutical Consulting – Quality that HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device |
Keywords | ASMF, Active Substance Master File, US-DMF, Drug Master File, Certificate of suitability, CEP, CTA ,Clinical Trial Application, IND, Investigational New Drug Application, CTD, Common Technical Document, European MAA |
WebSite | horn-pharma.de |
Host IP | 188.64.60.202 |
Location | Germany |
Site | Rank |
horn-druck.de | 0 |
horn-immo.de | 12,404,719 |
goldeneshorn.ch | 33,235,040 |
Euro€1,653
Zuletzt aktualisiert: 2022-08-18 16:09:08
horn-pharma.de hat Semrush globalen Rang von 22,298,223. horn-pharma.de hat einen geschätzten Wert von € 1,653, basierend auf seinen geschätzten Werbeeinnahmen. horn-pharma.de empfängt jeden Tag ungefähr 551 einzelne Besucher. Sein Webserver befindet sich in Germany mit der IP-Adresse 188.64.60.202. Laut SiteAdvisor ist horn-pharma.de sicher zu besuchen. |
Kauf-/Verkaufswert | Euro€1,653 |
Tägliche Werbeeinnahmen | Euro€35,815 |
Monatlicher Anzeigenumsatz | Euro€12,122 |
Jährliche Werbeeinnahmen | Euro€1,102 |
Tägliche eindeutige Besucher | 551 |
Hinweis: Alle Traffic- und Einnahmenwerte sind Schätzungen. |
Host | Type | TTL | Data |
horn-pharma.de. | A | 3600 | IP: 188.64.60.202 |
horn-pharma.de. | NS | 86400 | NS Record: ns1109.ui-dns.com. |
horn-pharma.de. | NS | 86400 | NS Record: ns1109.ui-dns.org. |
horn-pharma.de. | NS | 86400 | NS Record: ns1109.ui-dns.de. |
horn-pharma.de. | NS | 86400 | NS Record: ns1109.ui-dns.biz. |
horn-pharma.de. | MX | 3600 | MX Record: 10 mx00.kundenserver.de. |
horn-pharma.de. | MX | 3600 | MX Record: 11 mx01.kundenserver.de. |
Company Industries Consulting Project Management GXP Training Information HORN Pharmaceutical Consulting – Quality that matters! HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries. We offer a full spectrum of global consulting services and solutions from early phases of product development and clinical trials to submission of marketing authorization applications. Development of regulatory strategies, preparation of meetings with Authorities in EU and US, submission of dossiers [more] Preparation and review of CMC-documents: IMPD/IND, CTD for MAA/NDA [more] Project planning, guidance and advice for project teams [more] Services around GMP/GCP/GLP, development of SOPs, compliance checks [more] Clinical strategies, clinical documents, e.g IB, study protocol, study report, clinical overviews and summaries [more] Review of product development status, evaluation of development strategies, |
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