why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc
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What should be Step wise the sterlization procedure for Dry Powder injection facility (from Starting)?
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What are the steps for the sterilization procedure for Dry Powder injection facility (from Starting)?
what is purpose of slow,medium,fast sampling in process validation ?
what do you mean by mean kinetic temperature in stability
In KF Standardization why we use Disodium Tartarate?
what is the defination of Change Control given in various guidelines?
what is difference between in drug purity and drug potency
hai,i had completed my b.pharmacy.i want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at jyothipasam@gmail.com
at what interval Ukrainian audit will come once you register your product??
What is stationary phase?
How we fix the validity period of a Normal solution and re-standardization due date
what is limit of cleaning validation