Golgappa.net | Golgappa.org | BagIndia.net | BodyIndia.Com | CabIndia.net | CarsBikes.net | CarsBikes.org | CashIndia.net | ConsumerIndia.net | CookingIndia.net | DataIndia.net | DealIndia.net | EmailIndia.net | FirstTablet.com | FirstTourist.com | ForsaleIndia.net | IndiaBody.Com | IndiaCab.net | IndiaCash.net | IndiaModel.net | KidForum.net | OfficeIndia.net | PaysIndia.com | RestaurantIndia.net | RestaurantsIndia.net | SaleForum.net | SellForum.net | SoldIndia.com | StarIndia.net | TomatoCab.com | TomatoCabs.com | TownIndia.com
Interested to Buy Any Domain ? << Click Here >> for more details...

define process validation

Answer Posted / anuj sharma

Process Validation: Process validation is a procedure which
provide a high degree of confidence that the specific
process will produce the product of consistant quality and
will meet its predetermined specifications.

THANKS
ANUJ SHARMA
QA ISLL CHANDIGARH

Is This Answer Correct ?    8 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

Do you think it is possible to rehabilitate?

2213


what is the leak test procedure of filled bottles (liquid)

2212


Why SLS used as dissolution medium

1116


What is forced degradation study?

1241


how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis

9012


what is meant by artwork review and handling procedure with an example?

2098


Can any one tell me that which brand hplc column is used for levetiracetam imp- b test.

1857


please e-mail me the model of Tamil Nadu drug inspector question papers

2704


What r the different sop in or plant

1970


plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,

2433


How to do IR test of hydroscopic materials

1962


from hplc chromatogram how can we say that calibration is needed now?

2530


why you are become a medical representative

2176


Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section.

2703


How can I assign a retest date for solvents e.g. toluene, methanol, etc?

3029