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General Validation query!

What all can we validate in Pharma Industry?
Like system, process and so on… what else???

I do not understand your post.

What do you mean???

Hope I understood your post correctly. As a general rule, you can validate everything that implies a process, even administrative processes, if you want to. Per definition, when you validate, you are demonstrating the reproducibility and consistency of a process, i.e. its validity. Equipment and systems can be qualified for a given task, that means suitable, but that does not imply it performs that task in a reproducible way. What can be validated is the process the equipment or system performs, e.g. you can qualify a PW water generation and distribution system, and then validate the process of generation and distribution.

[quote=Sachin Patil]What all can we validate in Pharma Industry?
Like system, process and so on… what else???[/quote]

Well its better you elaborate the Question!!!

DEAR SACHIN
IN PHARMA ONDUSTRY
WE CAN VALIDATION.
PROCSS
ITS RELEATED EQUIPMENT ITS CLEANING
AREA INWHICH PRODUCTS R GOING TO MANUFACTURED.
PLC (PROGRAMMABLE LOGICAL CONTROLLER) IT IS PART OF EQUIPMENT VALIDATION.

WE HAVE TO QUALIFY RAW MATERIAL,ACTIVE MATERIAL,PACKING MATERIAL
ITS VENDOR,ITS ANALYSIS METHOD (ANALYTICAL METHOD DEVELOPMENT)

TRANSPORT VALIDATION (WE HAVE TO PERFORM).

REGARDS
PRASAD
prasadaparajit@rediffmail.com

[quote=Sachin Patil]What all can we validate in Pharma Industry?
Like system, process and so on… what else???[/quote]

[quote=pvalidation]DEAR SACHIN
IN PHARMA ONDUSTRY
WE CAN VALIDATION.
PROCSS
ITS RELEATED EQUIPMENT ITS CLEANING
AREA INWHICH PRODUCTS R GOING TO MANUFACTURED.
PLC (PROGRAMMABLE LOGICAL CONTROLLER) IT IS PART OF EQUIPMENT VALIDATION.

WE HAVE TO QUALIFY RAW MATERIAL,ACTIVE MATERIAL,PACKING MATERIAL
ITS VENDOR,ITS ANALYSIS METHOD (ANALYTICAL METHOD DEVELOPMENT)

TRANSPORT VALIDATION (WE HAVE TO PERFORM).

REGARDS
PRASAD
prasadaparajit@rediffmail.com[/quote]

how we will perform transport validation

For example, if you have a product that is temperature sensitive (say, a vaccine that needs to be maintained at 2 - 8 degrees Celsius) , one would have to document the maintenance of the cold chain from finished product manufacturing, packing, storage, despatch to warehousing, possibly even to final delivery of the product at the place of use/dispensing. One would have to validate the software used to manage these activities, as well as validate the cold chain, starting from manufacturing conditions to packing and finished product storage/quarantine, despatch, the containers used to ship the product to inventory, the warehousing storage space, etc. You get the picture.

This is just one example, there are numerous others, erp systems, etc…