The FDA (and eventually, regulatory agencies from around the world) will require clinical data sent to them to be in CDISC standards. Georgina Wood, ...
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”,...
The Navitas Life Sciences Networks are pleased to confirm the dates for our upcoming Autumn forums. At Navitas Life Sciences we have over 15 years’ experience in hosting and facilitating roundtable discussion ...
pharmaREADY is Navitas’ intuitive and easy to use, fully integrated, regulatory compliant, web-based suite comprised of modules for eCTD Publishing...
Navitas’ PVTech Summit was held on June 15th at the Hudson Hotel in New York City. The showcase focused on shaking up PV with new tools...
Navitas Life Sciences is pleased to welcome Tara Baer, who joins Navitas’ Regulatory Practice. With over 20 years’ experience...
David Gwyn, Navitas’ Technology Practice lead, will unveil idmpREADY at the Sparta Connection conference in Orlando, Florida...
In two different sessions, Subject Matter Experts from Navitas Life Sciences will address new challenges facing the life science industry created by the acceleration of the globalization of the life science industry...
Navitas’ inaugural pvindia meeting took place in Mumbai on Thursday 03 March, 2016. The event was well attended with 25 drug safety professionals representing 14 pharmaceutical companies...
Navitas Life Sciences will soon be adding to our portfolio of industry leading networks with the launch of pvindia; a network for Heads of Safety of Indian life sciences companies with pharma, consumer, generics, or mixed portfolios...