define process validation
Answers were Sorted based on User's Feedback
Answer / 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 |
Answer / sai
Process Validation is the term used to indicate that the a
process has been subject to scrutiny that the result of the
process (outcome)of a product is practically gauranteed.
Briefly-- the product meeting its predetermined reqirements.
| Is This Answer Correct ? | 5 Yes | 1 No |
Answer / umesh wangikar
Documented evidence which provides a high degree of assurance that a specific process will consistently result in a product that meets its predetermined specifications and quality characteristics.
UMESH WANGIKAR
MUMBAI
| Is This Answer Correct ? | 2 Yes | 0 No |
Answer / ravindra
Process Validation means that your process which give high
degree of assurance that the process Consistantly gives the
product within the predetermine specification & quality
attributes
| Is This Answer Correct ? | 2 Yes | 0 No |
Answer / suresh babu
Establishing by objective evidencethat a process
consistentlyproduces a result or product meeting its
predetermined requirements.
| Is This Answer Correct ? | 1 Yes | 0 No |
Answer / alexander
Process Validation ; Sumarised Data of Validated Process cross checked at every interval of Formulation Having Written Evidence From Both QA & QC
| Is This Answer Correct ? | 1 Yes | 0 No |
Answer / sandeep gaikwad
Process validation is defined as the collection and evaluation of data, from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products
| Is This Answer Correct ? | 0 Yes | 0 No |
How to perform forced degradation on tablet sample or suspensions?
when we connect the capacitor banks in series with the circuit? 2 144 pH is having unit?
How to register or submit drug master file to any regulatory agency?
Tolerance limit for dissolution media rpm sampling point.
how many persons involed for an internal audits?and who will audit the qa persons?
What is the difference between Deviation and Out of Specification ?
What experience do you have in training?
what is the leak test procedure of filled bottles (liquid)
what do you call "talking while sleeping at night" in english langusge?
How do you fix the known and unknown impurity limit for a drug substance?
human body absorbs maximum amount of nutrients in
why u want join cipla company as a medical representative