CTIS
CTIS is a Brazilian retail chain organization with emphasis in computer products.
CTIS
Industry:
Consulting Information Technology
Founded:
1983-01-01
Address:
BrasÃlia, Rio Grande Do Norte, Brazil
Country:
Brazil
Website Url:
http://www.ctis.com.br
Total Employee:
1001+
Status:
Active
Contact:
(61) 3212-9500
Technology used in webpage:
Viewport Meta IPhone / Mobile Compatible SPF SSL By Default Google Font API Google Analytics WordPress Content Delivery Network Google Universal Analytics Font Awesome
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Official Site Inspections
http://www.ctis.com.br Semrush global rank: 82.45 K Semrush visits lastest month: 1.28 M
- Host name: 200.99.40.39
- IP address: 200.99.40.39
- Location: Brazil
- Latitude: -22.8305
- Longitude: -43.2192
- Timezone: America/Sao_Paulo
More informations about "CTIS"
Clinical Trials Information System | European Medicines Agency …
Jan 31, 2022 The Clinical Trials Information System (CTIS) supports the flow of information between clinical trial sponsors, European Union (EU) Member States, European Economic …See details»
How to register with OMS to be able to work with …
What is the process to register an organization with OMS? If an organization is not yet registered with OMS when starting to use CTIS, the registration must be carried out.See details»
Step-by-step guide - European Medicines Agency
After users perform searches for both OMS and CTIS without finding their organisations, listed in the results, they will be able to create them locally in CTIS. This step-by-step guide explains …See details»
Support - EMA - Europa
The European Medicines Agency’s (EMA) Service Desk provides a dedicated, online helpdesk for clinical trial sponsors and regulators requiring technical support with using CTIS. Are you …See details»
About the clinical trials website - EMA
CTIS is a registered data provider for the World Health Organization (WHO). Data from authorised trials published on this website is included in the search portal of WHO's International Clinical …See details»
Clinical Trials - Icelandic Medicines Agency
Oct 17, 2023 The conduct of clinical trials in countries of the EEA will change significantly since the regulation on clinical trials entered into force on 31 January 2022. From this time on, it will …See details»
EU CTR: Clinical Trials Information System (CTIS) | PPD
Jan 31, 2022 CTIS user management To meet the needs of the different types of sponsor organizations that will use CTIS, two user management approaches exist from which sponsors can select: i) organization-centric and ii) trial …See details»
CTIS: general information | Investigators | The Central ... - CCMO
A main characteristic of the CTR is an application procedure via a single entry point- an EU portal and database (CTIS), for all clinical trials to be conducted in the EU/EEA. Information and …See details»
Clinical Trial Information System: overview, opportunities ... - PPD, …
ABSTRACT The implementation of the Clinical Trial Information System (CTIS), from 31 January 2022, will facilitate the day-to-day business of sponsors of clinical trials by harmonising …See details»
CTIS - Ready or Not, Here It Comes - Clinical Trials Arena
CTIS is the online system for the regulatory submission, authorisation and supervision of clinical trials in the EU and the European Economic Area. It is a single-entry point for all clinical trial data. As of 31 January next year, the use …See details»
CTIS First Optimapharm Experiences
CTIS has presented new opportunities for making trials run more efficiently, bringing transparency to clinical studies, improving collaboration between stakeholders, and enhancing regulatory …See details»
Register clinical trials in CTIS | Staff Portal - KI
All clinical trials are registered in the EU-joint web portal Clinical Trials Information System (CTIS). Everything regarding your clinical trial is managed within the portal; applications to the Medical …See details»
CTIS Part II: Document Management Best Practices for CTR …
Feb 7, 2023 The focus of this blog is specifically on the impact of CTIS on document management for sponsors and we will offer recommendations for best practices to maintain …See details»
Guidance and Q&As - EMA
The Clinical Trials Information System (CTIS) supports the business processes of clinical trial sponsors and national regulators throughout the lifecycle of a clinical trial, via secure …See details»
CTTM15 - FAQs - European Medicines Agency
The European Medicines Agency developed this training material to enhance public access to information on the Clinical Trial Information System (CTIS). This material describes a …See details»
Transition to the new EU CTIS Portal for Regulatory Clinical Trial ...
The Platform used for submission, either Portal de Ensayos Clínicos con Medicamentos from the Agencia Española del Medicamento (AEMPS) or CTIS, has been determined for each CT. All …See details»
Global Compliance Portal
On February 23, 2024, the EMA released an updated version (Version 2.0) of the CTIS Evaluation Timelines. The objective of this document is to provide an understanding of all the deadlines …See details»
EU Clinical Trial Regulation: What, When, Who, Why, How?
Learn how the EU Clinical Trial Regulation (CTR) will enhance clinical trials, improve transparency, and streamline collaboration for better patient safety.See details»
Three cities honoured for public health achievements at 2025 ...
3 days ago Today, during the annual Partnership for Healthy Cities Summit in Paris, three cities were recognized for their achievements in preventing noncommunicable diseases and injuries: …See details»
US deports hundreds of Venezuelans despite court order
6 days ago The White House says it has removed Venezuelan gang members and denies violating a court order.See details»