Pharmaceutical validation & it's types

Pharmaceutical validation & it's types ppt

1. VALIDATION & IT’S TYPES Presented by: Alexa Jacob 1 st yr M.Pharm Department of pharmaceutics St.joseph’s college of pharmacy,cherthala 1

2. CONTENTS 2

3. DEFINITION Validation means rectification or confirmation. Validation can be defined as a procedure that demonstrates that a process under standard conditions is capable of consistently producing a product that meets the established product specifications. 3

4. TYPES 4

5. 1) ANALYTICAL METHOD VALIDATION Method validation must prove that the analytical method used for a specific test is suitable for which it is to be carried out. Methods should be validated when:- When they are to be established for routine use. When the method is to be changed due to change in conditions. Whenever the equivalence between new method and the standard are demonstrated 5

6. TYPES OF PROCEDURES TO BE VALIDATED 1) ACCURACY:- The accuracy of an analytical method refers to the closeness of agreement between the observed value and the value which is either conventially a true one or reference one. 2 ) PRECISION:- The precision of an analytical method refers to the closeness of values obtained from a series of tests. 3) REPEATABILITY:- Repeatability is established when the same sample is estimated repeatedly by the same analyst using same analytical method within the same laboratory using same instrument and performed within a short period of time. 6

7. 4) INTERMEDIATE PRECISION:- When the test is repeated on different days by different persons or using different instruments within the same laboratory,the variation is expressed in terms of intermediate precision. 5) REPRODUCIBILITY:- When a method is standardized,the test is carried out in different laboratories using the same method,the precision between the laboratories is refered to as reproducibility. 6) SPECIFICITY:- Specificity is the ability of a test method to measure the analyte explicity in the presence of other components. 7

8. 7 ) LINEARITY:- Linearity of an analytical method refers to it’s ability to measure a specific component within a range. 8) DETECTION LIMIT 9) QUANTITATION LIMIT 10) ROBUSTNESS 11) RANGE 8

9. 2) EQUIPMENT VALIDATION Equipment validation is to provide a high level of documented evidence that the equipment and the process confirm to a standard. TYPES 9

10. It ensures that all major processing and packing equipment and ancillary systems are in conformity with installation specification,equipment manuals ,schematics Important IQ considerations :- Calibration,preventive maintenance Safety features Software documentation Equipment design features (a) INSTALLATION QUALIFICATION (IQ) 10

11. It is done to provide a high degree of assurance that the equipment functions as intended. It is conducted in 2 stages- component operational qualification & system operational qualification. Important OQ considerations :- Software procedures Raw material specification Process operation procedures Material handling requirements (b) OPERATIONAL QUALIFICATION (OQ) 11

12. It is a documented review of the design, at an appropriate stage in the project, for conformance to operational and regulatory expectation. Important DQ considerations are:- GMP’s and regulatory requirements Reliability and efficiency Safety and environment impact Construct ability and installation of equipment (c) DESIGN QUALIFICATION (DQ) 12

13. It is a documented verification that all aspects of a facility, utility or equipment perform as intended in meeting pre-determined acceptance criteria. Important PQ considerations:- Actual product & process parameters Acceptability of the product Process repeatability Long term process stability (d) PERFORMANCE QUALIFICATION(PQ) 13

14. 3) CLEANING VALIDATION Cleaning validation ensures that there is no cross contamination in a multi-product manufacturing plant and also prevents microbial contamination Once a product is manufactured,the equipment is cleaned using appropriate cleaning SOP’S established during IQ of the equipment TYPES OF CONTAMINATION TO BE CONSIDERED IN CLEANING VALIDATION Cross contamination Microbial contamination Contamination by cleaning or sanitizing agent Contamination by other agents 14

15. 4) PROCESS VALIDATION Process validation is the means of ensuring & providing documentary evidence that processes are capable of repeatedly & reliably producing a finished product of the required quality. TYPES 15

16. It is conducted prior to the distribution of either a new product or a product made under a modified production process, where the modifications are significant & may affect the product characteristics. It includes:- Initial stages of formulation devolepment & process devolepment Setting of process sampling plans Designing of batch records Defining raw material specifications Transfer of technology from scale up to commercial size batches Environmental controls (a) PROSPECTIVE VALIDATION 16

17. Here, the validation protocol is executed before the process is put into commercial use. It is generally considered acceptable that three consecutive batches within the finally agreed parameters,giving product of the desired quality would constitute a proper validation of the process. 17

18. It is a process where current production batches are used to monitor processing parameters. It gives of the present batch being studied, and offers limited assurance regarding consistency of quality from batch to batch. Examples of these may be when:- A previous validated process is being transferred to a third party contract manufacturer or to another site (b) CONCURRENT VALIDATION 18

19. The number of batches produced are limited Process with low production volume per batch and market demand The product is a different strength of a previously validated product with the same ratio of active or inactive ingredients 19

20. It is conducted for a product already being marketed and is based on extensive data accumulated over several lots and over time. This validation may be used for older products which were not validated by the fabricator at the time that they were first marketed. Retrospective validation is only acceptable for well established detailed processes and will be inappropriate when there have recent changes in the formulation of the products,operating procedures,equipment & facility. (c) RETROSPECTIVE VALIDATION 20

21. Some of the essential elements of this validation are:- Batches manufactured for a definite period Number of lots released per year Master manufacturing/packaging documents List of process deviations,corrective actions & changes to manufacturing documents Data for stability testing for several batches 21

22. Process re-validation is required when there is a change in any of the critical process parameters , formulation,primary packaging components,major equipmenta or premises Examples when process re-validation is required when:- Changes in raw materials ( physical properties such as density,viscosity,particle size distribution) Changes in source of active raw material manufacturer (d) PROCESS RE-VALIDATION 22

23. Changes in packaging material ( primary container/ closure system) Changes in the process (Mixing time,drying temperatures & batch size) Changes in the equipment Changes in the plant/facility 23

24. REFERENCE Industrial pharmacy , A Comprehensive approach, by D.K Tripathi , Pg no: 671-699 Pharmaceutical process validation : An overview , by M.d Shoaib Alam etal;Journal of advanced pharmacy education & research , oct-dec 2012,vol 2, issue 4, pg no: 190-196 24

25. THANKYOU… 25