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(9)Ce marking of medical devices
Pallavi Christeen
•
Vor 4 Jahren
INTELLECTUAL PROPERTY RIGHTS
Pallavi Christeen
•
Vor 3 Jahren
Regulatory requirements for CE CERTIFICATION of Medical Devices in European Union
Pallavi Christeen
•
Vor 3 Jahren
21CFR 320- BIO AVAILABILITY AND BIO EQUIVALENCE REQUIREMENTS
Pallavi Christeen
•
Vor 4 Jahren
Marketing Authorization procedures in developed and developing countries
Akshay Saxena
•
Vor 8 Jahren
Dossier preparation and submission
Doninder Hooda
•
Vor 6 Jahren
Drug approval process for US & India
AnumulaSurendra
•
Vor 7 Jahren
Pharmacy act 1948
CHALAPATHI INSTITUTE OF PHARMACEUTICAL SCIENCES
•
Vor 5 Jahren
Menstrual disorders
Dr Zharifhussein
•
Vor 10 Jahren
Personal Information
Beruf
student
Tags
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
Mehr anzeigen