1. Presented By : Guided By : Ch.Mahesh Babu.Mrs.Mcthel M.PHARMACY Asst.professor Dept of pharmaceutics NIRMALA COLLEGE OF PHARMACY

2. Stability testing is an integral part of pharmaceutical development. The primary purpose of stability testing is to provide supporting evidence on stability behavior of pharmaceutical drug products. Many factors drive the process of industrial stability testing for pharmaceutical development.

3. It is an evolutionary concept covering the life cycle of pharmaceutical product development. In early discovery phase the primary focus is to generate stability characteristics of a chemical /biological entity. In later stages,the goal is to establish shelf life for formulations packaged in final package intended for commercial introduction.

4. Discovery phase Pre clinical stage Pre-IND stage IND stage Product development stage NDA stage Approved product stage Revised product stage

5. DISCOVERY PHASE To help select the most satisfactory chemical entity possessing the right pharmacological, toxicological & pharmaceutical profile. The pharmaceutical profile is mostly focused towards the optimum chemical and physical stability characteristics. To select the right physical form(base, salt,ester) These studies help establish the boundaries with in which one must operate to design formulations.

6. The development of early dosage form for pre clinical testing in humans require an extensive stability evaluation. Preliminary stability testing on all formulations must be carried out using stability indicating assays in accordance with GLPs. It requires an entrance assay prior to the initiation of toxicological testing and an exit assay, must be performed at the end of the studies.

7. Pre-formulation & stability evaluation of chemical entity is carried out according to ICH guidelines. In addition to normal preformulation evaluations,forced degradation studies under highly stressed stability conditions is under taken. DOSAGE FORMPARAMETERS SOLIDTemperature, humidity, photo degradation. solutionspH, ionic strength, additives

8. Accelerated and normal storage temperature testing of drug substance and for clinical formulation must be initiated. The goal of these studies should be to generate information to insure that the clinical formulations are likely to remain stable during the planned clinical studies.

9. Intermediate stability testing is done in this stage. Interim stability testing is conducted to establish the maximum time for which a drug product can be stored in interim containers for further processing.

10. Formal stability program is established for generation of stability data for registration applications. The stability of drugs should be evaluated in containers used for marketing. Care should be exercised in selection of the size, surface-to volume ratio of the container.

11. The goal of the stability evaluation program during this phase is to confirm or extending the expiration date. The commitment in this stage mandates that any batch that is found out of specification will be with drawn from the market.

12. Most products undergo post approval changes. They may be internally driven or externally driven. Internally driven : changing size & shape of dosage forms, changes in package design and others. Externally driven : deletion of dyes, formulation changed and others.

13. Establishment of stability testing function requires an extensive development of documentation to maximize the compliance and to minimize the regulatory citations.

14. The guidelines in section 211.166 of 21 CFR states there shall be a written stability testing program designed to assess the stability characteristics of drug product. a written stability testing program is critical for the establishment of the stability testing function.

15. The stability protocol should record the purpose for conducting the stability test the method used, the testing frequency,storage conditions and several other factors. The commitment requires submission of stability data at periodic intervals as specified in the application.

16. Current good manufacturing practices mandate that every organization develops a set of SOPs to describe their operations. It is almost impossible to develop a stability management function with out having a comprehensive set of SOPs

17. Regulations require that each person engaged in the manufacturing processing should have education or training to enable that person to perform the assigned functions. Training shall be in the particular operations that the employees performs. Training must be conducted by qualified individual on a continuous basis with sufficient frequency.

18. During discovery phase stability evaluation is used in the conduct of pre-clinical safety. This data helps to establish retest period for drug substances. Selection of three pilot batches is used for statistical evaluation.

19. Based on the analysis the world is divided in to 4 climatic zones.

20. W ORLDWIDE ZONES AND THE TEMPERATURE AND HUMIDITY CONDITIONS ZoneMean kinetic temperature Yearly average humidity (%RH) Zone I ( Moderate) 21 ̊ C 45 Zone II (Mediterranean) 25 ̊ C 60 Zone III (Hot, dry) 30 ̊ C 35 Zone IV (Very hot, moist) 30 ̊ C 70

21. C OUNTRIES BELONGING TO VARIOUS ZONES RegionsZone I &IIZone III&IV EUROPEAll countries AMERICAArgentina, Bolivia, Canada, Mexico, US Brazil, Columbia, Cuba, Jamaica ASIAAfghanistan, China, Iran, Nepal, Turkey Bahrain, Hong Kong, India, Oman, Pakistan, Srilanka,UAE AFRICAEgypt, Algeria, South Africa, Libya Angola, Benin, Congo, Uganda, Sudan, Somalia, Senegal

24. Study Storage condition Minimum time period covered by data at submission Long Term (Ambient) 25º C ± 2º C 60%RH ± 5% 12 months Intermediate (controlled) 30º C ± 2º C 60%RH ± 5% 6 months Accelerated 40º C ± 2º C 75%RH ± 5% 6 months

25. To simulate the transportation and shipment conditions in the stability studies thermal cycling is done Testing parameters for those studies should include not only the chemical analysis but also physical changes.

26. Photostability testing studies include: Test on drug substance. Test on exposed drug product outside the immediate pack. Test on drug product in the immediate pack. Test on drug product in the marketing pack. Light source Option 1: Artificial daylight lamp combining both visible & UV output similar to D65 & ID65. Option 2: Cool white fluorescent & near UV lamp output max. energy emitted

27. Sample exposed to light source/actinometric system Eg: Quinine chemical actinometry 2%w/v aq.solution of quinine monohydrochloride dihydrate Option 1: In 20ml colourless ampoule at 400 nm Option 2: In 1cm quartz cell-(sample) and control wrapped with Aluminium foil Change in absorbance calculated by A = AT-A0

29. Photostability testing Forced degradation Confirmatory testing Evaluate the photosensitivity Its used alone or in solution Placed in chemically inert & transparent containers. Variety of exposure condition Information necessary for handling, packaging and labeling To study, identify precautionary measures needed in manufacturing or in formulation

30. The containers should be tested in all directions i.e..up right,inverted,on the side positions. This is done for long term and accelerated stability testing. This is to ensure that there are no adverse effects from any interaction is produced.

31. For long-term storage 12 month study Testing frequency 0 3 6 9 12 For accelerated storage 6 month study Testing frequency 0 3 6 (initial) (final) If significant change occur Increase the testing by adding sample at final time point Include 4 th time point in study design For intermediate storage 12 month study - Testing frequency 0 6 12 If significant change occur - A 4 th time point can be included

32. According to the section 211.166 of 21 CFR states that testing of drug products for re constitution at the time of dispensing as well as after they are reconstituted. For reconstituted products two distinct stability periods are in operation. First period: long term and accelerated stability testing prior to reconstitution. Second period: short term stability after reconstitution

33. Dosage formEvaluation TabletsAppearance,colour,odour,assay,degra dation products,dissolution,moisture and friability. Hard gelatin capsulesAppearance,colour,odour,assay,degra dation products,dissolution,moisture and microbial limits Soft gelatin capsulesAppearance,colour,odour,assay,degra dation products,dissolution,moisture and microbial limits,pH,leakage. EmulsionsAppearance,colour,odour,assay,degra dation products, microbial limits,PH,viscosity,preservative content and distribution of dispersed phase globules.

34. Dosage formEvaluation Oral solutionsAppearance,colour,odour,assay,degrad ation products, PH,microbial limits, preservative content. Oral suspensionsAppearance,colour,odour,assay,degrad ation products, PH,microbial limits, preservative content,redispersibility,rheological properties, mean size and distribution of particle. Oral powdersAppearance,colour,moisture,and reconstitution time. Inhalations and nasal spraysAppearance,colour,odour,assay,degrad ation products, dose content uniformity, microscopic evalution,water content, leak rate, microbial limits. Topical,opthalamic,ointments,creams,l otions,pastes,gels,solutions. Appearance,clarity,colour,homgeneity, odour,ph,resuspendibility,viscosity,par ticle size distribution,assy,degraation products,preservatives,microbial limits, weight loss.

35. Dosage formEvaluation Small volume parenteralsAppearance,colour,clarity, assay,presarvative content, degradation products, particulate matter, sterility, Large volume parenteralsAppearance,colour,clarity, assay,presarvative content,degradation products,particulate matter,sterility,pH,pyrogeni city,volume.

36. Bracketing is the design of a stability schedule such that samples on the extremes of certain design factors are tested at all time points. Protocols for bracketing designs should be endorsed by the FDA prior to initiation of primary stability studies (FDA 1998). Bracketing design is suitable and applicable to identical or closely related formulations packaged in different size identical container/closure system.

37. MATRIXING Matrixing is the design of a stability schedule such that the selected subset of the total number of possible samples for all factor combinations would be tested at a specified time point. 3 rd month 6 th month