Regulatory Affairs & Life Science

Skupno trajanje:1 h 22 min

	What Companies should know about PMCs and Biocidal Products	Regulatory Affairs & Life Science	07:02
	Pharmacovigilance Responsibility: Who Watches Over Our Medicines?	Regulatory Affairs & Life Science	06:56
	The use of Data Mining in PMCF data analysis and real-world questionnaires	Regulatory Affairs & Life Science	06:35
	Medical Devices: Rising Costs and Regulatory Complexity After Seven Years of IVDR and MDR	Regulatory Affairs & Life Science	07:32
	The Role of Statistics in the Drafting of a Post-Market Clinical Follow-Up (PMCF) Plan for Medical Devices	Regulatory Affairs & Life Science	09:46
	Good Clinical Practice new version published	Regulatory Affairs & Life Science	05:16
	Working in the pharmaceutical sector	Regulatory Affairs & Life Science	10:13
	Authorisation for the organisation of Pharmaceutical Conferences and Meetings	Regulatory Affairs & Life Science	08:47
	Parallel importation of medical devices	Regulatory Affairs & Life Science	07:20
	QPPV: A Guardian of Drug Safety	Regulatory Affairs & Life Science	06:19
	Regulation (EU) 2017/745 (MDR)	Regulatory Affairs & Life Science	06:58