Ectd

Ectd: 229 results found.

Arzneimittelregistrierung,Polen,Registrierung,Arzneimittel,Medizinprodukte,Biozide, CRO, Pharmacovigilance, CTD, eCTD-Dossiers,Zulassungsanträge,Updates,Regulatory-Affairs
Registrierung der Arzneimittel und Medizinprodukte in Polen, Erstellung von CTD- und eCTD-Dossiers, Zulassungsanträgen, Wiederzulassungsanträgen und Updates, Pharmacovigilance, CRO in Polen.
Farchimpol.de ~ Site Info Whois Trace Route RBL Check

医薬品開発、eCTDを支援する株式会社PPGオフィシャルサイト
株式会社PPG（Pharma Projetista Group）のオフィシャルサイトです。当社では、医薬品開発、医療機器開発、市販後対策、eCTD導入などのサポートを行っております。
Pharm-projetista.com ~ Site Info Whois Trace Route RBL Check

GlobalSubmit Home
GlobalSubmit is the leader in the development and implementation of electronic submissions based on the eCTD format. The system is used exclusively by the FDA and leading global life sciences companies.
Wisewomenplan.com ~ Site Info Whois Trace Route RBL Check

eCTD, Electronic Common Technical Document, CTD, Common Technical Document, Regulatory, Medical Writing, ISI
ISI guides life sciences companies through the changing technology and regulatory landscape with flexible software solutions, innovative professional services, and in-depth knowledge enabling enterprises to reach new levels of efficiency and speed throughout the electronic submissions process.
Forms2pdf.com ~ Site Info Whois Trace Route RBL Check
Similar Sites: imagesolutions.com - isicopy.com - isicopy.net

Outsource Software Development and IT offshore company India-Sarjen System Pvt Ltd
Offshore Software Developement and IT outsourcing company with Developement Center in India and We develop Web applications,web sites and software solutions for Pharmaceutical companies. We work on J2EE,.NET,PHP and VB technology.Outsourcing of software development, offshore web development, outsourcing projects in Microsoft ASP.NET, PHP, J2EE
Sarjen.com ~ Site Info Whois Trace Route RBL Check

Preparing for the New Global Requirements for eCTD and Regulated Product Submissions Mastering the Tools and Strategies
Paper submissions are losing traction and that's no secret. Every day regulatory authorities across the globe are turning to electronic submissions as their new preferred format ... and the FDA is leading the way. With RPS (Regulated Product Submission) poised to build on the eCTD standard, if you don't yet have your electronic submission process perfected, there's no time to lose. Many drug, biologic and device companies can already measure the difference in dollars — through increased first time acceptance rates, shorter FDA review times, and yes, speed to market.
Ectdworkshop.com ~ Site Info Whois Trace Route RBL Check

Home | Kompass Regulatory
Kompass Regulatory Services provides an extensive portfolio of regulatory and clinical affairs services including a full eCTD and NeeS compilation and publishing service.
Kompassreg.com ~ Site Info Whois Trace Route RBL Check

| イーサ株式会社|ヘルスケア・ライフサイエンス・医療の現場をIT技術で効率的にする
イーサ株式会社は、アットコアード、ミケテンプレートなどの製品およびアウトソーシング等のサービスを提供し、IT技術でeCTD申請などの作業を効率化します。
Esaplus.com ~ Site Info Whois Trace Route RBL Check

医薬品関連書籍/本/治験
医薬品関連の本、書籍、出版物、印刷物等のご紹介、治験（ちけん）/臨床試験/副作用/新薬モニターについての解説をしています。
Book189.com ~ Site Info Whois Trace Route RBL Check

LORENZ Life Sciences: The e-Regulatory Affairs Experts
LORENZ is the most established provider of e-regulatory software and services in the world, providing solutions for eCTD, SPL and more.
Docubridge.com ~ Site Info Whois Trace Route RBL Check
Similar Sites: drugtrack.com - lorenz.cc