Eggs in the infective stage of the chicken nematode Ascaridia galli are often required for in vivo andin vitro studies on this parasite. The reliability of any artificial A. galli infection depends on the viability and embryonation capacity of A. galli eggs. The aim of this study was to determine ideal storage conditions for maximising the viability of A. galli eggs and maintaining viability for the longest period. A 2 × 2 × 3 × 5 factorial experimental design was employed to investigate the effects of storage temperature (4◦C or 26◦C), storage condition (aerobic or anaerobic), storage medium (water, 0.1 N H2SO4 or 2% formalin) and storage period (4, 8, 12, 16 and 20 weeks). The viability of eggs was assessed after eggs in all treatment groups were held aerobically at 26◦C for 2 weeks after the storage period to test embryonation capacity. Based on morphological characteristics, they were categorised as undeveloped, developing, vermiform, embryonated or dead. The maintenance of viability during storage at 4◦C was optimal under anaerobic conditions while at 26◦C it was optimal under aerobic conditions. Anaerobic conditions at 26◦C led to a rapid loss of viability while aerobic conditions at 4◦C had a less severe negative effect on maintenance of viability. Egg storage in 0.1 N H2SO4 resulted in a significantly higher viability overall (54.7%) than storage in 2% formalin (49.2%) or water (37.3%) (P < 0.0001). Untreated water was the least favourable storage medium when eggs were stored at 26◦C while it was a medium of intermediate quality at 4◦C. The viability of A. galli eggs decreased significantly with storage time (P < 0.0001) depending on the other factors. The lowest rate of decline was seen with storage of eggs under anaerobic conditions at 4◦C or aerobic conditions at 26◦C in 0.1 N H2SO4. Eggs in these treatments retained up to 72% of overall viability at 20 weeks with a decline rate of approximately 2% per week with no significant difference between the two. Therefore, this study has clearly revealed opposing aerobic conditions required for prolonged storage of A. galli eggs in the preembryonated state at 4◦C. It has also identified that 0.1 N H2SO4 provides the best preservation against degradation during storage, particularly at 26◦C under aerobic conditions. Achieving strictly anaerobic conditions can be difficult to achieve so storage aerobically at 26◦C may be preferred for simplicity.