Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5517061 | Biologicals | 2017 | 5 Pages |
â¢The consistency approach is a primal way for batch release without animal testing.â¢Transition to this approach raises barriers but fortunately also drivers.â¢A workshop was held to identify and better understand the drivers and barriers.â¢This report summarises the outcome of the workshop.â¢Recommendations are to improve the regulatory process for the consistency approach.
Safety and potency assessment for batch release testing of established vaccines still relies partly on animal tests. An important avenue to move to batch release without animal testing is the consistency approach. This approach is based on thorough characterization of the vaccine, and the principle that the quality of subsequent batches is the consequence of the application of consistent production of batches monitored by a GMP quality system. Efforts to implement the consistency approach are supported by several drivers from industry, government, and research, but there are also several barriers that must be overcome. A workshop entitled “Consistency Approach, Drivers and Barriers” was organized, which aimed to discuss and identify drivers and barriers for the implementation of the 3Rs in the consistency approach from three different perspectives/domains (industry, regulatory and science frameworks). The workshop contributed to a better understanding of these drivers and barriers and resulted in recommendations to improve the overall regulatory processes for the consistency approach. With this report, we summarise the outcome of this workshop and intend to offer a constructive contribution to the international discussion on regulatory acceptance of the consistency approach.