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

6 years ago • 2660 Views

Ce marking of medical devices

5 years ago • 1562 Views

Regulatory requirements for CE CERTIFICATION of Medical Devices in European Union

5 years ago • 1359 Views

INTELLECTUAL PROPERTY RIGHTS

5 years ago • 251 Views

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Ce marking of medical devices

Pallavi Christeen • 5 years ago

INTELLECTUAL PROPERTY RIGHTS

Pallavi Christeen • 5 years ago

Regulatory requirements for CE CERTIFICATION of Medical Devices in European Union

Pallavi Christeen • 5 years ago

21CFR 320- BIO AVAILABILITY AND BIO EQUIVALENCE REQUIREMENTS

Pallavi Christeen • 6 years ago

Marketing Authorization procedures in developed and developing countries

Akshay Saxena • 9 years ago

Dossier preparation and submission

Doninder Hooda • 7 years ago

Drug approval process for US & India

AnumulaSurendra • 8 years ago

Pharmacy act 1948

CHALAPATHI INSTITUTE OF PHARMACEUTICAL SCIENCES • 6 years ago

Menstrual disorders

Dr Zharifhussein • 12 years ago
Personal Information
Occupation
student
Tags
regulatory european union ce mark declaration of conformity usfda medical devices maa regulatory requirements gmdn intellectual property rights patent industrial design trademark copyright geographical indication bapatla college of pharmacy cgpdtm wipo paris treaty patent act government india innovation information technology control
See more