An important phase during the pharmaceutical development is the transformation of the active substance into a finished dosage form that is adequate for its administration in humans and its release is suitable from efficacy (bioavailability) and safety (toxicity) point of view. In this phase, the galenical development acts.
What Netpharmalab offers to you…
Professionals with more than 13 years of experience in the galenical development endorse the Netpharmalab’s expertise in this field.
We provide support and advice in the development and optimization of formulations, development and optimization of manufacturing processes, technology transfer and manufacturing of industrial processes.
Our experience along these years covers all pharmaceutical forms, especially modified release dosage forms (pellets, matrix, osmotic pumps, etc.).