Regulatory Affairs & Life Science

Regulatory Affairs & Life Science

Por: Di Renzo Regulatrory Affairs
The Di Renzo Regulatory Affairs podcast for pharmaceutical companies, for manufacturers of medical devices, cosmetics, food supplements and disinfectants. News from our blog and from our weekly magazine ISI, Information Health.
22 episodios disponibles

Latest episodes of the podcast Regulatory Affairs & Life Science

Biocides in 2025 New Rules, New Responsibilities 03/10/2025
MIR 7.3.1: Everything Manufacturers Need to Know Before November 2025 19/09/2025
Pharmacovigilance Goes Social 12/09/2025
Classification of medical devices in Italy 21/08/2025
Top Registration Mistakes That Could Cost Your Medical Device Approval 30/07/2025
Local pharmacovigilance: all requirements, how to be compliant 25/07/2025
Is our software a Medical Device? 02/07/2025
Labelling pharmaceutical sectors 10/06/2025
Are our cosmetics labels compliant 30/05/2025
Statistics and Post-Market Surveillance: Ensuring Medical Device Safety 22/05/2025
Food supplements regulation in Italy 15/05/2025
What Companies should know about PMCs and Biocidal Products 09/05/2025
Pharmacovigilance Responsibility: Who Watches Over Our Medicines? 07/04/2025
The use of Data Mining in PMCF data analysis and real-world questionnaires 28/03/2025
Medical Devices: Rising Costs and Regulatory Complexity After Seven Years of IVDR and MDR 21/02/2025
The Role of Statistics in the Drafting of a Post-Market Clinical Follow-Up (PMCF) Plan for Medical Devices 14/02/2025
Good Clinical Practice new version published 24/01/2025
Working in the pharmaceutical sector 17/01/2025
Authorisation for the organisation of Pharmaceutical Conferences and Meetings 07/01/2025
Parallel importation of medical devices 14/11/2024
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