Concerned Member State (CMS)

Other countries that may perform their own reviews of an application for approval during or after the reference member state has reviewed the application.

    More information about Concerned Member State (CMS)

    Decision,decentralised procedure,products,procedures,submission,time,Mutual recognition procedure,company,medicinal product,timelines.

    Assessment procedure,period,report,medicine,documents,market,mutual recognition,Centralised procedure,zonal procedure,health,public health,authorisation period,validation period,active substances,assessment reports,draft assessment report.

    Agency,Community,issues,notice,Notice to Applicants,package leaflet,Co-ordination Group,major amendments,national marketing authorisation,cover letter,regulatory requirements,cell therapies,positive opinion,Economic Area,centralized procedure,60-day procedure.

    Application procedure,RUP procedure,0-Day procedure,60-day arbitration procedure,60-days procedure,abbreviated procedure,administrative procedure,appeal procedure,coordinated procedure,Decentralised procedure form,decentralized procedure,European authorisation procedures,grievance procedures,Marketing authorisation procedures,meaningful procedures,mutual recognition reliance procedure,National procedure,health plan,quality of health care,animal health,health care provider,health care services,health care standards,health condition,health quality experts,high-quality health care,national health authority,innovative products,product applications,Applicants of products,application for product registration,authorisation for products,biotechnology products,history of product,medicinal product documentation,opinion on products,31-day period,45-day assessment period,45-day period,45-day period MSs,5-day period,contract period,period for CTs concerning,period of performance,submission of draft responses,actual submission,COMMON SUBMISSION PLATFORM,Dedicated submission,electronic submissions,Instruction for submission Documentation,interval between submission,national submission,substances,chemical substances,low-risk substances,active substance dossier,low-risk active substance,draft report,5-digit company number,applicant company,company responses,class of medicines,approval of medicines,orphan medicine requirements,document requirements,Draft response documents,outcome documents,procedural timelines,legal timeline,maximum timelines,single decision,class waiver decision,time frame,application for time slots,EMA European Medicines Agency,European Medicines Agency,market authorisation,market for sale,Community Authorisation,patients at Community level,availability issues,outstanding issues,model notice plans.

    Why trust Agatha Life during your clinical trials?

    Every day, more than 200 companies trust Agatha to manage their clinical trial documentation
    Mablink
    Gustave Roussy
    Beyond Spring
    Clinical Services
    NS Pharma
    Share via
    Copy link
    Powered by Social Snap