Regulatory Updates | Kirsten Van Garsse, Authorized Representative Director & Regulatory Affairs Manager IVD (4)

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Kirsten Van Garsse, Authorized Representative Director & Regulatory Affairs Manager IVD

Recent Posts

Nuevas normas armonizadas publicadas para el cumplimiento de MDR e IVDR

Propuestas de modificación de IVDR y MDR: disposiciones transitorias, implantación de EUDAMED e interrupciones de la cadena de suministro

El Consejo de la UE aprueba la propuesta de modificación de los Reglamentos IVDR y MDR

Visión general de los requisitos lingüísticos de IVDR/MDR para fabricantes de productos sanitarios

New EMA FAQ on the Development and Assessment of Medicinal Products Involving Companion Diagnostics (CDx)w EMA FAQ on medicinal products development and assessment involving a CDx

Events calendar

June

24.06 - 26.06

CPHI China

26.06 - 27.06

PDA Advanced Therapy Medicinal Products Conference (Europe)

July

27.07 - 31.07

ADLM

August

29.08 - 01.09

ESC Congress

September

07.09 - 11.09

LSI Europe

17.09 - 17.09

Farmaforum

23.09 - 23.09

BioWin day

25.09 - 25.09

29.09 - 01.10

TOPRA annual Symposium

October

07.10 - 08.10

World Drug Safety Congress

07.10 - 10.10

RAPS US Convergence

16.10 - 16.10

Healixia Clinical Conference

19.10 - 20.10

Annual EU In Vitro Diagnostics Clinical & Regulatory Conference (Q1)

23.10 - 23.10

23.10 - 24.10

Team-PRRC Annual Summit

25.10 - 28.10

TCT 2025

28.10 - 30.10

CPHI Europe

November

17.11 - 20.11

Medica

December

11.12 - 11.12

Dutch Life Science conference