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globalsubmit.com
GlobalSubmit eCTD Submissions Software | Certara
Whether you are experienced or new to the regulatory submission process, the risk of rejection of your electronic common technical document (eCTD) submissions cannot be taken lightly, especially given the changing and growing complexity of the regulatory environment. Not to mention, differences i

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ectdoffice.com

eCTD Office - eCTD (NeeS / VNeeS) Publishing Software Solution

Mono eCTD Office is a suite of integrated NeeS / eCTD software products for the validation, creation, viewing, manipulation and archiving of NeeS / eCTD submissions of regulatory documentation by pharmaceutical companies to the regulatory authorities.

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impactpharma.com
Syner-G BioPharma Group
The world’s leading CMC & Regulatory Affairs solutions provider for biopharma. Consulting solutions in CMC 360, global regulatory affairs & medical writing.

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cunesoft.com
Phlexglobal, A Pharmalex Company
Authoritative eTMF Software and Outstanding TMF Expert Services Are Our Core Proposition to Ensure Inspection-Readiness with Less Effort and Less Risk.

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fdaagents.com
registrarcorp.com
registrarcorp.com

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extedo.com
Home | EXTEDO
EXTEDO RIM Solutions - Software and expertise to efficiently manage your regulated documents, data, and processes within the life science industry.

Moz DA: 30 Moz Rank: 3.6 Semrush Rank: 2,608,675
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lorenz.cc
Regulatory Affairs Solutions Experts | LORENZ Life Sciences Group
The specialist for Regulatory Information Management solutions geared towards industry, health authorities and academia since 1989!

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ectdresource.com
Home - eCTD Resource
Under construction. Come back soon!

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fdaatty.com
FDA Attorney In Washington D.C. & Portland OR | FDA Atty
FDA Atty is a Washington D.C. law firm specialized in FDA laws & regulations. Our FDA attorney team will help you get you FDA-ready. Contact us.

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fdabasics.com
FDA registration And Regulatory Compliance Services FDABasics
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pharmaready.com
eCTD & eDMS Submissions Software, Regulatory Pharmaceutical Electronic Document Management System - pharmaREADY
PharmaReady™ is a fully integrated web-based eDMS and eCTD Submissions Solution Suite. PharmaReady is specifically designed for regulated Life Science organizations where ease of installation, ease of use, compliance and affordability are primary business drivers. PharmaReady is available is in both on-site and remote-hosted implementations.

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pharmdevgroup.com
Pharmaceutical Development Consultant and Consulting Services | PDG
Pharmaceutical Development Group (PDG) is your pharmaceutical consultant, consulting services for U.S. FDA submission, launch and post-approval strategic product planning services. Our collective knowledge and experience spans a variety of dosage forms and therapeutic areas. Contact PDG for help with your next project.

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aquilasolutions.us
eCTD Regulatory Publishing, Consulting, and Strategy
Need assistance on your regulatory journey? Need a better understanding of eCTDs and the process? Reach out to Aquila Solutions now!

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kingbeintl.com
Kingbe International Online
Kingbe International is a management consulting company specializing in international trade and logistics. Our professional managers provide customers with over 60 years of international industry experience. We provide specific solutions

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exalon.com
Exalon - eCTD-Experts
Exalon - eCTD-Experts

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fda-registration.com
FDA Registration & US Agent Service for non-US manufacturers of pharmaceutical and medical devices, foods and food products offered by Wellkang® LLC - FDAagent.us - FDA-Registration.com
FDA Registration & US Agent Service: FDA U.S. Agent services for non-US manufacturers of pharmaceutical and medical devices, foods and food products offered by Wellkang® LLC - FDAagent.us - FDA-Registration.com

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hartmannwillner.com
HartmannWillner | FDA regulatory consulting firm
HartmannWillner | FDA regulatory consulting firm

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usagentservices.com
Foreign Food Facility Registration Compliance FDA | US Agent Services
Foreign Food Facility Registration US Agent FDA Compliance Services. If your company is outside the U.S. but sells food in the US FSMA requires registration

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samarindrms.com
Instem - Samarind RMS - Regulatory Information Management
The benchmark for Regulatory Information Management

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regardd.org
ReGARDD
ReGARDD Project

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acutallc.com
Regulatory Compliance
Automate regulatory compliance operations and information management, boost efficiencies and improve performance across your global product portfolio.

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mdiconsultants.com
FDA Consultants | Medical device consultants
FDA consulting for the medical device industry, pharmaceutical industry and food industry for US and EU FDA quality assurance.

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freyrsolutions.com
Global Regulatory Solutions and Services Company
Freyr is a Global Regulatory Solutions and Services company, focusing on the entire Regulatory value-chain ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions to post approval maintenance, Labeling, Artwork Change Management for Pharmaceutical, Generics, Medical Device, biotechnology, Biosimilar, Consumer Healthcare, Cosmetic companies across the globe.

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gphaonline.org
Gphaonline.org

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ectdtips.com
eCTD Tips - Tips, advice, and news about regulatory submissions in eCTD format.
Tips, advice, and news about regulatory submissions in eCTD format.

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techlinkinternational.com
Techlink International Inc. | NOM Compliance
Your Trusted Source for Compliance

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ijpcbs.com
International Journal of Pharmaceutical and Chemical Sciences
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rosettaectd.com
ROSETTA Regulatory Information Management and eCTD Software by DoubleBridge Technologies, Inc.
ROSETTA regulatory software for viewing, reviewing and tracking of regulatory submissions prepared in eCTD format for the life sciences industry and regulatory agency

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topra.org

TOPRA - The Organisation for Professionals in Regulatory Affairs

TOPRA is the professional membership organisation for individuals working in healthcare regulatory affairs worldwide.

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sbiaevents.com
SBIA Events | US FDA Small Business & Industry Assistance Events
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docshifter.com
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Compliant, fast, automated, and scalable document conversion for the regulated enterprise. On-premise or in your private/hybrid cloud.

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fdasolutionsgroup.com
FDA Solutions Group
FDA registration, fda compliance, FDA, food, drug

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qservegroup.com
Global Market Access for Medical Devices - Qserve Group
Qserve is your MedTech Consultant for Regulatory Affairs & Quality Assurance and Clinical Trials. Need regulatory advice, support or training? Contact us.

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iriss-forum.org
IRISS

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ectd247.com
ectd247 – Simple, fast and cost-effective cloud-based solution to build and track your eCTD submissions.
ectd247 - Simple, fast and cost-effective cloud-based solution to build and track your eCTD submissions.

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fdamap.com
FDA MAP - FDA Regulatory Consulting Services | FDA Compliance Consultant | Seminars and Conferences
FDAMap offers FDA regulatory consulting services and FDA compliance training programs like FDA workshop, seminars, conferences, regulatory advisory and onsite GMP audit.

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biomapas.eu
BIOMAPAS | Baltics and Eastern Europe CRO
Privati sutartinių mokslinių tyrimų organizacija (SMTO), teikianti klinikinių tyrimų paslaugas farmacinėms ir biotechnologinėms kompanijoms.

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qumas.com
Life Sciences and Material Sciences | BIOVIA – Dassault Systèmes
Powered by the 3DEXPERIENCE® platform, BIOVIA delivers scientific software that helps life and materials sciences professionals model the biosphere

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ich.org
ICH Official web site : ICH
ICH Official web site : ICH Creationist organization. The Institute for Creation Research (ICR) is a creationist apologetics institute in Dallas, Texas, that specializes in media promotion of pseudoscientific creation science and interpretation of the Genesis creation narrative as a historical event. The ICR adopts the Bible as an inerrant and literal documentary of scientific and historical fact as well as religious and moral truths, and espouses a Young Earth creationist worldview. It rejects evolutionary biology, which it views as a corrupting moral and social influence and threat to religious belief. The ICR was formed by Henry M. Morris in 1972 following an organizational split with the Creation Science Research Center (CSRC).Its work in the field of creation science has been rejected by mainstream science, but has been significant in shaping creationist thought in the United States by introducing creation science through fundamentalist churches and religious schools, and by engaging in public debates against supporters of evolution. The ICR also offers unaccredited graduate level programs in Biblical Apologetics, including a minor in Creation Research.

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kenblockconsulting.com
FDA and Regulatory Consulting to Medical Device Makers Worldwide
With offices in the US and Japan, Ken Block Consulting helps medical device manufacturers achieve success in the US market through FDA compliance.

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Cassady-Susan HOME
Cassady-Susan HOME

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ectdviewer.pro
Mono eCTD Viewer - Free eCTD Lifecycle Viewer - Mono eCTD Office
Mono eCTD Viewer is a FREE, stand-alone, super-fast, easy to use Windows desktop software application for re-viewing and understanding the granularity and the lifecycle of electronic submissions prepared in the eCTD (Electronic Common Technical Document), NeeS (Non-eCTD), (veterinary) VNeeS and other electronic dossier formats.

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alvamed.com | Medtech Compliance Solutions
| Medtech Compliance Solutions

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weinberggroup.com
Press Releases - ProPharma
Catch up on Press Releases and other special announcements about ProPharma and our subsidiaries.

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ipqpubs.com
International Pharmaceutical Quality (IPQ)
International Pharmaceutical Quality (IPQ)

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dms-jp.com
株式会社ディジタルメディアシステム
株式会社ディジタルメディアシステムは、システム構築におけるソフトウェア開発やコンサルタントなど、お客様の幅広いニーズにお応えいたします。QuarkXPress Quark XTensions デベロッパー、docuBridge 日本総販売代理店

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fdahelp.us
How to get FDA Registration - FDA Certificate
FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API or medical device in the USA.

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diaztradeconsulting.com
Home - FDA USA
Home - FDA USA

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namsa.com
NAMSA | Medical Device Contract Research Organization
The world's only 100% medical device-focused, full development Contract Research Organization (CRO). Learn how to accelerate your development program today!

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World Food Connection – Getting your food products into the U.S. market
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cspscanada.org
Home - Canadian Society for Pharmaceutical Sciences
THANK YOU TO OUR SPONSORS IN THE NEWS TODAY Covering topics important to our members and the profession. Late Breaking Abstract Submissions are

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Ennov | Content & Information Management Platform for Life Sciences
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EAS serves the industries of Food (including USDA), Pharmaceutical, Dietary Supplements, Medical Device, Tobacco, Biologics, Cannabis, and Cosmetics.

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Gens home
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We are a boutique Life

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