Professional Documents
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Pharmaceutical
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Cofinanciado por:
Blinding strategies
management
Registration Dossier
Orphan Drug designation
application (EMA and FDA)
Placebo manufacturing
Labeling, primary and
secondary packaging
Formulation
Development
Tech
Transfer
API
Selection
GMP
Compliant
Clinical batches
Manufacturing
Quality
Control and
Batch
Release
Stability
Studies
Clinical
Trial Logistics
Management
Clinical
Trials
Registration
Dossiers
Analytical
Development
SERVICES
PROVIDED
BY IDIFARMA
TECHNOLOGICAL SOLUTIONS
Development and validation
of analytical methods
Active substance and
reference product
characterization
Quality control and
validation of the
manufacturing process
Film coating
Conventional or high
potency (cytotoxic,
hormonal, )
Microtablets
Lyophilization
Manufacturing process
optimization at GMP facilities
Photostability studies
Modified release
Chewable, Orodispersible
Liposomes
Spray drying micro and nano encapsulation