From fifteen to future – Navitas Networks 15 year anniversary
Wednesday, 05 July 2017

Navitas industry networks recently celebrated its milestone 15th year of delivering insights and creating dialogue to address industry challenges and benchmark practices...

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Life Sciences expert Navitas augments end-to-end capabilities
Friday, 09 June 2017

Navitas, a technology-led Life Sciences services provider across Clinical, Regulatory and Safety, announced that it would be augmenting its capabilities with the niche expertise of its legacy brands,...

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ICH Reflection on “GCP Renovation”: Modernization of ICH E8 and Subsequent Renovation of ICH E6 January 2017
Thursday, 20 April 2017

Navitas Life Sciences welcomes the opportunity to provide comments on this Reflection Paper...

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Navitas Life Sciences Augments Global Executive Management Team
Thursday, 13 April 2017

Navitas Life Sciences announced the appointment of Dr. Krishnan Rajagopalan as Chief Growth Officer. As the Chief Growth Officer, Krishnan will oversee Navitas’ sales and marketing efforts,...

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Navitas Networks announce Forum dates for Spring, 2017
Tuesday, 24 January 2017

The Navitas Life Sciences Networks are pleased to confirm the dates for our upcoming Spring forums...

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Navitas Launches Labeling Assessment Express
Tuesday, 17 January 2017

Regulators are changing the way they look at labeling. The emphasis is on ensuring Marketing Authorization Holders have a linked up End-to-End (E2E) process...

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BioVectra chooses pharmaREADY for eCTD Solution
Wednesday, 02 November 2016

BioVectra has chosen pharmaREADY for its eCTD requirements. BioVectra, located in Canada, manufactures ingredients for global pharmaceutical and biotechnology clients, ...

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Navitas Life Sciences at DIA’s 10th Annual Forum for Qualified Persons in Pharmacovigilance conference in the United Kingdom
Wednesday, 05 October 2016

Navitas Life Sciences Principal Jeffrey Ho will present "Efficient content management for the compilation and management of the PSMF" at the DIA 10th Annual Forum , ...

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Navitas Life Sciences releases paper on CDISC, the standards and why the upcoming December 18th FDA deadline matters
Tuesday, 27 September 2016

The FDA (and eventually, regulatory agencies from around the world) will require clinical data sent to them to be in CDISC standards. Georgina Wood, ...

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AbbVie and Navitas Life Sciences Present Case Study on the Evolution and Transformation of PV Organizations
Tuesday, 13 September 2016

At 10:30a.m. (East Coast Time) on September 22nd, Navitas Life Sciences and AbbVie will present “PV Organizations Reimagined – Roadmap to Transforming into a Strategic PV Organization”,...

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