Cogem

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Contained Use Deliberate Release Market Authorisation

Advice following the European consultation on the authorisation process of GMOs in medical applications
COGEM advice Containment levels for laboratory activities involving lenti- and retroviral vectors
Inactivation of GM plant material

Highlighted publications

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20.08.2021

Advice following the European consultation on the authorisation process of GMOs in medical applications

CGM/210820-01

Advisory reports
24.03.2021

Generic environmental risk assessment of clinical trials with MVA vectors

CGM/210324-01

Advisory reports
22.03.2021

What is known about the import, distribution and presence of GM oilseed rape (Brassica napus) in the Netherlands?

CGM 2020-02

Research reports
01.07.2020

COGEM advice concerning the proposal by the EC to suspend the environmental risk assessment of clinical trials for the treatment or prevention of COVID-19

CGM/200624-01

Advisory reports
07.05.2020

The COGEM formula revisited, experimental validation of the reduction ratio formula for free lentiviral particles

CGM 2020-01

Research reports
11.02.2020

Generic environmental risk assessment of clinical trials with AAV vectors

CGM/190905-01

Advisory reports

Ongoing projects

16.09.2021

Advice on the proposal to adapt the monitoring strategy for GM carnations

expected | 06.10.2021