Revalidation in the pharmaceutical industry is very important as it helps to maintain the validated status of the equipment, plant, manufacturing process as well as the computer systems. This procedure is necessary for periodic checking of the validation results according to the revalidation period.
This process is mandatory by law for quality assurance purposes. While validation is a process of collecting and documenting the information about the operating parameters, revalidation focuses on ensuring that the product quality remains unaffected by the changes in the process machinery methods and scale-ups, process environment etc.
Revalidation is classified further as:
1. Scheduled periodic revalidation according to the revalidation period as per the government regulations.
2. Revalidation after a change in the product, process, plant or manufacturing process.
Scheduled periodic revalidation refers to revalidation which must be carried out in a pharmaceutical plant at regular intervals. It is often mandatory when the company makes any changes to the procedures, formulas, equipment, manufacturing process, packaging material or manufacturing support systems like water and steam.
Related: How to Write a Validation Protocol?
For which changes does revalidation become necessary?
1. When the raw material is changed: If changes are made to the starting material of the product, then the revalidation process must be initiated. It is also necessary to revalidate in case the physical properties of the raw materials are modified. It includes modification in the viscosity, crystal properties, particle size and specific gravity of the active ingredients as well as the excipients.
2. Packaging material changes: A revalidation is required when the packaging material of the medicine or product is changed. Although packaging material may not have an adverse effect on other physical goods, it is an important factor in the case of pharmaceuticals. If the packaging material which comes in direct contact with the dosage is changed then it may have an effect on the stability and quality of the medicine.
3. Manufacturing process changes: If any changes are done to the manufacturing process like a change in the timing or sequence of processes, cooling time, temperature variations, then revalidation is required.
4. Change in equipment: If new equipment is introduced into the plant or changes are made to existing instruments, then it can change the accuracy of measurements of the raw materials. This can affect the manufacturing process to a great extent. Hence it is necessary to do revalidation in this case.
The pharmaceutical industry is a very important part of the health and fitness industry. Certain drugs and medicines can spell the difference between a person’s life and death. For this reason, it is necessary to take proper care to ensure the validation and revalidation processes are as effective as possible.
This process is mandatory by law for quality assurance purposes. While validation is a process of collecting and documenting the information about the operating parameters, revalidation focuses on ensuring that the product quality remains unaffected by the changes in the process machinery methods and scale-ups, process environment etc.Revalidation is classified further as:
1. Scheduled periodic revalidation according to the revalidation period as per the government regulations.
2. Revalidation after a change in the product, process, plant or manufacturing process.
Scheduled periodic revalidation refers to revalidation which must be carried out in a pharmaceutical plant at regular intervals. It is often mandatory when the company makes any changes to the procedures, formulas, equipment, manufacturing process, packaging material or manufacturing support systems like water and steam.
Related: How to Write a Validation Protocol?
For which changes does revalidation become necessary?
1. When the raw material is changed: If changes are made to the starting material of the product, then the revalidation process must be initiated. It is also necessary to revalidate in case the physical properties of the raw materials are modified. It includes modification in the viscosity, crystal properties, particle size and specific gravity of the active ingredients as well as the excipients.
2. Packaging material changes: A revalidation is required when the packaging material of the medicine or product is changed. Although packaging material may not have an adverse effect on other physical goods, it is an important factor in the case of pharmaceuticals. If the packaging material which comes in direct contact with the dosage is changed then it may have an effect on the stability and quality of the medicine.
3. Manufacturing process changes: If any changes are done to the manufacturing process like a change in the timing or sequence of processes, cooling time, temperature variations, then revalidation is required.
4. Change in equipment: If new equipment is introduced into the plant or changes are made to existing instruments, then it can change the accuracy of measurements of the raw materials. This can affect the manufacturing process to a great extent. Hence it is necessary to do revalidation in this case.
The pharmaceutical industry is a very important part of the health and fitness industry. Certain drugs and medicines can spell the difference between a person’s life and death. For this reason, it is necessary to take proper care to ensure the validation and revalidation processes are as effective as possible.
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If I validate a process in some equipments and than want to run the same process in some other equipments of same plant with same batch size, do I need to revalidate it as per PMDA and USFDA guidelines?
ReplyDeleteYes in these conditions you have validate the process again.
DeleteYou should add revalidation conditions in process validation protocol.
ReplyDeletei have some tempreture related issue in coating machine,i have very small range for outlet temreture 32 to 35..it can change by revalidation
ReplyDeleteYou can change the range using a change control if your product doesn't have any problem with increase temperature.
DeleteWhat is difference between continuous process verification (as per FDA) & APQR
ReplyDeleteWhat is difference between continuous process verification ( as per FDA) & APQR ( annual product quality review)
ReplyDeleteContinued process verification include the analysis of the quality of raw materials, in-process material and finished products while annual product quality review analyze only finished product.
DeleteI have doubt
ReplyDeleteMy batch size is 100.00kg to 200.00kg, as revalidation we perform 200.00kg batches in 3 run, after validation we take 150.00kg batches it's possible
Dear Sir, For scheduled periodic revalidation is it required to keep stability sample?
ReplyDeletevery excellent thanks alot.
ReplyDeleteNew water system has introduced in our company is it necessary to do revalidation to all produxts
ReplyDelete