Generic drug usually means a drug that has the same qualitative and quantitative composition of the active ingredient and the same pharmaceutical form as the reference branded drug, and whose bioavailability with the reference drug has been demonstrated by an appropriate…
Process Validation for Aceclofenac 100mg and Paracetamol 500mg Tablets
According to Indian GMP validation study is essential part of GMP. Those required to be done as per predetermined protocols. Prospective process validation1, 2 is carried out during the development stage by means of risk analysis of the production process which…
Studies In Process Validation For IBUPROFEN 200mg & ETHOCARBAMOL 500mg Caplets Dosage Formulation
According to Indian GMP validation study is essential part of GMP. Those required to be done as per predetermined protocols. Prospective process validation1, 2is carried out during the development stage by means of risk analysis of the production process which is…
Formulation and in vitro evaluation of theophylline-Eudragit®sustained-release tablets
In the last few years controlled release dosage forms have made significant progress in terms of clinical efficacy and patient compliance. The objective of designing a controlled release system is to deliver drug at a rate necessary to achieve and maintain…