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aqui explica todo sobre herramientas para el desarrollo de software.
Proper documentation is the backbone of compliance in pharma-grade solvent supply chains. Maintainin...
Documentation in technology transfer covers technology transfer plan, technology transfer report,pro...
This summarizes the ICH Q11 and covers the major topics of this guideline. For brief overview please...
All information about Drug Master File(DMF)
A patent search is the process of checking existing patent literature to find prior art that is simi...
cGMP GUIDELINES ACCORDING TO SCHEDULE M
Navigating medical device registration in Brazil for Class III devices can be complex. This presenta...
Antic Egipte 3-
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ICH GUIDELINES Q8, QbD
Pure Global offers comprehensive assistance with ANVISA Brazil medical device registration, ensuring...
Pure Global aids in navigating the complexities of ANMAT Argentina medical device registration, a cr...
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This slide cover basic aspects , regulatory body and marketing authorisation process in uk and Euro...
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quality by design
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Informations Regarding Investigators Brouchers & IMPD, Contents, Applications
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Documentation in Pharmaceutical Industry - master formula record , DMF ( DRUG MASTER FILE )
