The Navitas pharmaREADY TMF Consulting team can provide strategic planning and support in implementing an electronic centralized method of compiling, storing and archiving the TMF documents. The Navitas pharmaREADY Document Management System is equipped with customizable Trial Master File Templates that capture searchable document metadata enabling instant access to all the stake holders and document owners.The Navitas pharmaREADY TMF Consulting team is highly qualified to assist sponsors in organizing and implementing compliant Trial Master Files. The team provides practical guidance on file organization that will facilitate management of the clinical trial, audit, and inspection.


Life Sciences expert Navitas augments end-to-end capabilities

Navitas, a technology-led Life Sciences services provider across Clinical, Regulatory and Safety, announced that it would be...


BioVectra chooses pharmaREADY for eCTD Solution

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


Navitas at DIA's 10th Annual Forum for Qualified Persons...

Navitas Principal Jeffrey Ho will present “Efficient content management for the compilation and management of the...


Navitas Celebrates 100th pharmaREADY customer

pharmaREADY is Navitas’ intuitive and easy to use, fully integrated, regulatory compliant, web-based suite comprised of modules...


Navitas Introduces Innovative Regulatory Process Outsourcing Model

The workload for regulatory functions of pharmaceutical companies has continued to increase in recent years ...