The Navitas Life Sciences Networks are pleased to confirm the dates for our upcoming Spring forums...
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...
BioVectra has chosen pharmaREADY for its eCTD requirements. BioVectra, located in Canada, manufactures ingredients for global pharmaceutical and biotechnology clients, ...
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 , ...
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...