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...

In pharmaceuticals formulation OOS applicable in Raw
Material(which is not manufacturing in the company. and
purchase by approved vendor)).Why?

Answer Posted / b.suresh naidu

Yes OOS is applicable in Raw materials (which is not
manufacturing in the company and purchased by approved
vendor).

OOS may be due to assignable (or) non-assignable causes,
which may occur due to analytical error, manufacturing
error, _ _. To identify the root cause, investigation
should be done.

In a formulation unit, upon observation of OOS in any Raw
material, preliminary investigation/retesting to be done as
per ‘In-house OOS’ procedure (The procedure should be
clearly defined in ‘In-House OOS’ SOP). The OOS should be
informed to the Vendor on the day of the
observation/Confirmation. It is the responsibility of the
Vendor to do further investigation (Vendor should have
their OOS procedure for OOS investigation).

Upon completion of investigation, the Vendor should
inform the same to the respective Formulation unit with
necessary CAPA.

Is This Answer Correct ?    15 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

pharma industries oriented

2296


if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?

1048


In rs method development when we are going area normalization method to dilute standard method?

1567


why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?

2362


What should be the level/ Percentage of Arsenic in Arsenic free zinc.

2276


How can I develope method of dissolution by HPLC OR UV

2457


If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?

1042


IS THERE ANY EQUIPMENT TO CHECK AND CALCULATE THE POLARITY OF A LIQUID?

2506


what is diffrence between specificity and selecivity?

837


[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?

849


What is the purpose of octyl silane columns?

4340


We use hicrome 10 cxs column in hplc analysis....pls tell me.. what is the meaning of 10 cxs?

1784


why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?

9889


Why a1% value is used for some product ? What is the criteria for selection a1% value ?

2395


how to set sample and standard concentration in RS method?

967