RIM Webinar: Accelerate Time to Value by Leveraging Predefined Regulatory Processes
Tuesday February 16, 2021 – 11:00 AM EST | 5:00 PM CET Join our free webinar to learn the benefits of leveraging our library of
Tuesday February 16, 2021 – 11:00 AM EST | 5:00 PM CET Join our free webinar to learn the benefits of leveraging our library of
Learn how Ennov Analytics Dashboards are used to manage risk, increase efficiency and improve insight.
Ennov is pleased to announce the launch of the Ennov Insider – a new, exclusive library of premium content available only to registered users. The
Learn how Ennov RIM and Documentum can operate effectively together in an enterprise system architecture.
Learn how Ennov RIM and Ennov PV are used to enable the efficient production of Periodic Safety Update Reports
Ennov are pleased to announce that the Danish pharmaceutical company Pharmacosmos has implemented Ennov Doc and Ennov Training for the management of their global Quality
Ennov is pleased to announce the addition of Steve Clark to our team of Regulatory experts. Steve has over 20 years of global Regulatory operations
The evaluation of safety signals should be a continuous process in pharmacovigilance and it is essential that Manufacturing Authorization Holders (MAH’s) have a well-defined process to capture, evaluate,
The MHRA Inspectorate Blog recently posted a post [i] discussing Corrective and Preventive Actions, the importance of root cause analysis, and what triggers inspectors to
Recently, I reviewed the results of the Gens & Associates’ World Class RIM Survey. There is a wealth of great information on RIM investments, benefits, practices,
FDA has issued a final guidance document on Civil Money Penalties Relating to the ClinicalTrials.gov Data Bank. This draft guidance was first issued in 2018
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