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Found 6277 results for any of the keywords ectd submissions. Time 0.027 seconds.

Best eCTD Software Tool for global eCTD Submissions

Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.
https://www.ectdtool.com/ - Details - Similar

Regulatory Affairs, Operations, Intelligence, Case Studies

Freyr s case studies on Regulatory Affaris and Operations, Regulatory intelligence, Submission and Publishing to FDA
https://www.freyrsolutions.com/case-studies?tid%5B%5D=18 - Details - Similar

Swixit - Regulatory Impact for Medical Devices Med Tech Industry

We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on “Swixit - Regulatory Impact for Medical Devices Med Tech Industry” was successfully concluded on March 23, 2022. Here is an archived
https://www.freyrsolutions.com/webinars/swixit-regulatory-impact-for-medical-devices-med-tech-industry - Details - Similar

Obligations for Economic Operators EOs | Freyr - Global Regulatory Sol

In June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
https://www.freyrsolutions.com/infographics/obligations-for-economic-operators-eos - Details - Similar

Swixit and Its Impact on the MedTech Industry

This article talks about the Swixit and its impact on the MedTech Industry and transitional timelines for various device categories.
https://www.freyrsolutions.com/blog/swixit-and-its-impact-on-the-medtech-industry - Details - Similar

Swissmedic s New Medical Device Regulations

This article talks about the Swissmedic’s new medical device regulations for manufacturers to successfully market their products in Switzerland.
https://www.freyrsolutions.com/blog/swissmedics-new-medical-device-regulations - Details - Similar

Regulatory Labeling | Freyr - Global Regulatory Solutions and Services

In June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
https://www.freyrsolutions.com/blog/category/regulatory-labeling - Details - Similar

Benefits of eCTD, Enhancing eCTD Submission Benefits | Freyr Submit PR

Freyr SUBMIT Pro is one of the best eCTD Submission software that suits all kinds of Regulatory eCTD publishing and submission requirements across the globe.
https://www.ectdtool.com/why-submit-pro - Details - Similar

SAHPRA - South African Health Products Regulatory Authority

SAHPRA is an entity of NDOH created by the SA government to ensure that health and well-being of humans and animals health are at its core.
https://www.sahpra.org.za/ - Details - Similar

eCTD publishing Software, eCTD validator, PDF Manager, Submission Trac

Freyr SUBMIT PRO eCTD tool is a prominent eCTD publishing Software with various features like Inbuilt eCTD validator and viewer, submission tracking, HA query management, rDMS integration and many more.
https://www.ectdtool.com/ectd-software - Details - Similar

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