Thans Mr.Tim for valued presentation: I have a question please: if media fill was done for eye drop with non-transparent bottle, then how we can detect the turbidity or growth at this stage?
@@timsandlemicrobiologist thanks a lot Mr.Sandle for your reply …. On the other hand , I have still two question. That being as debate with my client, and your reply will be added value for me : 1- is there need for separate sterile testing lab for Blow fill seal solution Manufacurering plant ( IV bag with sodium chloride )? 2- is there need for gowning as Class A for BFS room ( operator ) or not ?! Also, is there need for separation gowning and degowning rooms for blow fill seal room in case class A Gown used ? Thanks and appreciate ur effort
Sir would you please answer me a question? My question is " in case of cephalosporine facility, if the highest commercial batch is 15000 nos in 12 hrs is it permissible fill 18000 nos in 6 hrs?
Very useful introductory video
Thans Mr.Tim for valued presentation: I have a question please: if media fill was done for eye drop with non-transparent bottle, then how we can detect the turbidity or growth at this stage?
Hello, you need to switch to using an identical transparent bottle for the simulation.
@@timsandlemicrobiologist thanks a lot Mr.Sandle for your reply …. On the other hand , I have still two question. That being as debate with my client, and your reply will be added value for me :
1- is there need for separate sterile testing lab for Blow fill seal solution Manufacurering plant ( IV bag with sodium chloride )?
2- is there need for gowning as Class A for BFS room ( operator ) or not ?! Also, is there need for separation gowning and degowning rooms for blow fill seal room in case class A Gown used ?
Thanks and appreciate ur effort
Alguna literatura especifica para esta prueba?
Good stuff
Sir would you please answer me a question? My question is " in case of cephalosporine facility, if the highest commercial batch is 15000 nos in 12 hrs is it permissible fill 18000 nos in 6 hrs?