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NEWS

Feb 19

Company Information Change

Dear Costumers, Partners and Visitors of our pages,We are happy to introduce you to Infotehna's new corporate identity...
Jun 22

Infotehna signed an agreement with Swiss pharmaceutical company Ewopharma AG

Infotehna is pleased to announce its further expansion into new markets. Pharmaceutical company Ewopharma AG with its...
May 10

Infotehna has earned the 'Designed for EMC' re-accreditation via 'fast-path'

Infotehna platform myProcess has earned the Designed for EMC re-accreditation via "fast-path"! This demonstrates...

EVENTS

Jan 26

Infotehna Conference with Workshop: Advanced Process and Document Management in e-Submission, QA/QC and R&D - May 19-20, 2010 (Munich, Germany)

Where: Sheraton Munich Airport Hotel, Munich, Germany  When:  May 19 - 20, 2010Infotehna’s consultants with guest...
Mar 03

Infotehna Conference: Electronic Document & Submission Management in Veterinary Companies, May 21, 2010 - Munich, Germany

Where: Sheraton Munich Airport Hotel, Munich, Germany  When:  May 21, 2010Infotehna’s consultants with guest speakers...
Dec 16

12th Annual INFOTEHNA Pharmaceutical Conference, June 16-18, 2010 - Primosten/Split, Croatia

  Where: Hotel Zora, Primosten/Split, CroatiaWhen:  June 16 - 18, 2010 Internationally renowned speakers from EU...

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ewopharma logo

Infotehna signed an agreement with Swiss pharmaceutical company Ewopharma AG

Infotehna is pleased to announce its further expansion into new markets. Pharmaceutical company Ewopharma AG with its headquarters in Switzerland has engaged into the project of implementation of Infotehna's eCTDExpert in its subsidiary in Slovakia. Ewopharma AG is the successor company to Leclerc & Co. which was founded in 1959.

From the start the company has focused on the pharmaceutical markets of Central Eastern Europe. With more than 50 years presence in Poland, the Czech Republic, Slovakia, Hungary, Romania and Bulgaria and Slovenia they have gained extensive in-depth knowledge of these countries, enabling them to achieve a privileged position in the area.

More about Ewopharma

Infotehna’s eCTDExpert™ - The RIGHT Choice

eCTDExpert™ is a comprehensive solution that leverages Infotehna’s own compliance process control engine coupled with EMC/Documentum’s flagship content management technology. The solution delivers regulatory document control in accordance with cGMP and GAMP guidelines. In addition to its comprehensive document lifecycle workflow, cGMP change control, security model, audit trails, digital/electronic signature capability, version control, eCTDExpert™ includes an integrated input/capture and publishing capability for document rendering, publishing, and eCTD XML generation. The system is fully compliant 21 CFR Part 11 guidelines for closed systems and is validation ready. eCTDExpert™ delivers a total solution for regulatory affairs organizations.

Rapid Deployment and On Demand Technical Support

In support of eCTDExpert™ Infotehna provides comprehensive on demand services and technical support to ensure rapid deployment and system adoption. All Infotehna life sciences solutions are deployed in validated systems environments, thus we offer validation (IQ/OQ/PQ) protocols to support validation efforts.

To facilitate rapid deployment, Infotehna’s technical team stands ready to deliver tactical project management services, training, and migration services for a turnkey approach. Stop wasting time and money on “solutions” that require expensive customization and integration. Infotehna’s all-in-one eCTDExpert™ is designed to accelerate your return on investment and implementation. If your objective is compliance and you seek a cost effective solution for quality, R&D, regulatory, and marketing, look no further than Infotehna’s eCTDExpert™.

Learn more about eCTDExpert™

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