Pallavi Christeen
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regulatory declaration of conformity ce mark european union control information technology innovation india government patent act paris treaty wipo cgpdtm bapatla college of pharmacy geographical indication copyright trademark industrial design patent intellectual property rights gmdn regulatory requirements maa medical devices usfda
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21CFR 320- BIO AVAILABILITY AND BIO EQUIVALENCE REQUIREMENTS

il y a 4 ans • 1765 Vues

Ce marking of medical devices

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Regulatory requirements for CE CERTIFICATION of Medical Devices in European Union

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INTELLECTUAL PROPERTY RIGHTS

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Ce marking of medical devices

Pallavi Christeen • il y a 4 ans

INTELLECTUAL PROPERTY RIGHTS

Pallavi Christeen • il y a 3 ans

Regulatory requirements for CE CERTIFICATION of Medical Devices in European Union

Pallavi Christeen • il y a 3 ans

21CFR 320- BIO AVAILABILITY AND BIO EQUIVALENCE REQUIREMENTS

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Marketing Authorization procedures in developed and developing countries

Akshay Saxena • il y a 8 ans

Dossier preparation and submission

Doninder Hooda • il y a 6 ans

Drug approval process for US & India

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Pharmacy act 1948

CHALAPATHI INSTITUTE OF PHARMACEUTICAL SCIENCES • il y a 5 ans

Menstrual disorders

Dr Zharifhussein • il y a 10 ans
Personal Information
Profession
student
Mots-clés
regulatory declaration of conformity ce mark european union control information technology innovation india government patent act paris treaty wipo cgpdtm bapatla college of pharmacy geographical indication copyright trademark industrial design patent intellectual property rights gmdn regulatory requirements maa medical devices usfda
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