# \[e-drug\] Bio-Equivalence **URL:** \ **Category:** e-drug\ **Created:** [December 12, 2002, 11:46pm UTC](https://talk.edrugplus.org/t/e-drug-bio-equivalence/15683 "2002-12-12T23:46:00Z")\ **Posts on this page:** 1\ **Page:** 1
**Author:** ![ahsan](https://avatars.discourse-cdn.com/v4/letter/a/958977/32.png) [@ahsan](https://talk.edrugplus.org/u/ahsan)\ **Post date:** [December 12, 2002, 11:46pm UTC](https://talk.edrugplus.org/t/e-drug-bio-equivalence/15683/1 "2002-12-12T23:46:00Z")
E-drug: Bio-Equivalence --------------------------------------------- Dear Colleagues! I am interested to know if there are any pre-requisites of Bio-Equivalence Studies by various Drug Control/Regulatory agencies like USFDA, Canadian FDA, MCA UK and other similar agencies. What are the specific generics or groups which require such a pre-requisite of Bio-Equivalence studies before being considered for granting registration/permission to market? Are there any WHO guidelines available on the subject? Naziruddin Ahsan Secretary Pharmacy Council of Pakistan Islamabad, Pakistan. ahsan@pharmacy.isb.sdnpk.org -- To send a message to E-Drug, write to: e-drug@usa.healthnet.org To subscribe or unsubscribe, write to: majordomo@usa.healthnet.org in the body of the message type: subscribe e-drug OR unsubscribe e-drug To contact a person, send a message to: e-drug-help@usa.healthnet.org Information and archives: [http://www.essentialdrugs.org/edrug](http://www.essentialdrugs.org/edrug)