Freyr SUBMIT PRO September 30, 2024
Freyr Digital September 25, 2024
Freyr rDMS September 18, 2024Did you know An effective eDMS enhances compliance…
Freyr SUBMIT PRO August 30, 2024In regulatory submissions, the difference between a flawless, on-time submission and one riddled with delays often comes down to one key factor:…
Freyr Digital August 16, 2024In today’s fast-paced regulatory environment, staying compliant is more challenging than ever. Enter Artificial Intelligence (AI), a game-changer…
Freyr SUBMIT PRO August 12, 2024As we step into 2024, the pharmaceutical and life sciences industries are rapidly transforming. A growing demand for regulatory affairs (RA)…
Freyr rDMS July 25, 2024In the Pharmaceutical Industry, Regulatory Documents are meticulously checked and consulted for the sake of public health care.
Freyr SUBMIT PRO July 25, 2024The idea of electronic regulatory submissions for pharmaceuticals predates the eCTD tool itself. In the late 1980s, initiatives such as CANDA (…
Freyr rDMS July 17, 2024The life science industry plays a significant role in maintaining public health and medical emergencies which is why there are thorough checks on…
Freyr SUBMIT PRO July 12, 2024Electronic Common Technical Document (eCTD) submissions are a cornerstone in the life sciences industry, enabling streamlined and efficient…
Freyr Digital July 2, 2024Over the years, international organizations and the pharmaceutical industry have observed the detrimental effects it has on the environment.…
Freyr SUBMIT PRO June 19, 2024The world of pharmaceutical regulations is about to get a major upgrade with the implementation of eCTD 4.0. This standardized format promises a…
