Post by Donic Chien-Sheng Lu
PMO Supervisor at Anivance AI Corporation
"๐๐ก๐ฒ ๐๐ซ๐ ๐๐ง-๐จ๐ง-๐-๐๐ก๐ข๐ฉ ๐ข๐ฌ ๐ญ๐ก๐ '๐๐ฎ๐ซ๐ฏ๐ข๐ฏ๐๐ฅ ๐๐๐๐๐ง๐ฌ๐' ๐๐จ๐ซ ๐๐๐๐ฌ ๐๐ง๐ ๐ญ๐ก๐ '๐๐ฎ๐๐๐๐ฌ๐ฌ ๐๐ง๐ ๐ข๐ง๐' ๐๐จ๐ซ ๐๐ก๐๐ซ๐ฆ๐." Despite decades of advancement, ๐ง๐๐๐ซ๐ฅ๐ฒ ๐๐% ๐จ๐ ๐๐ซ๐ฎ๐ ๐๐๐ง๐๐ข๐๐๐ญ๐๐ฌ that enter clinical trials fail to reach approval. The industry is at a crossroads. Traditional animal testing is becoming an "๐จ๐ฎ๐ญ๐๐๐ญ๐๐ ๐ฌ๐ญ๐๐ง๐๐๐ซ๐" of high risk and low predictability. With the ๐ ๐๐ ๐๐จ๐๐๐ซ๐ง๐ข๐ณ๐๐ญ๐ข๐จ๐ง ๐๐๐ญ ๐.๐ green-lighting new approach methodologies, providing only animal data is now synonymous with providing high-risk data. ๐๐ซ๐ ๐๐ง-๐จ๐ง-๐-๐๐ก๐ข๐ฉ (๐๐จ๐): ๐๐ก๐ ๐๐ฎ๐ซ๐ฏ๐ข๐ฏ๐๐ฅ ๐๐๐๐๐ง๐ฌ๐ For CROs, an OoC platform is no longer an "extra expense"โit is a strategic necessity. ๐๐ฎ๐ฆ๐๐ง-๐๐๐ง๐ญ๐ซ๐ข๐: The leading standard for human physiological simulation. ๐๐๐๐ข๐ฌ๐ข๐ฏ๐ ๐๐ฒ๐ง๐๐ซ๐ ๐ฒ: Use OoC to obtain decisive results first, followed by more precise, targeted animal testing. This reduces waste and accelerates timelines. ๐ ๐ฎ๐ญ๐ฎ๐ซ๐-๐๐ซ๐จ๐จ๐: Transition from a "testing vendor" to a "risk-reduction partner." Stop reinforcing the 90% failure rate. Itโs time to provide human-relevant certainty. #Anivance #Biotech #CRO #FDA #OrganOnAChip #DrugDiscovery #Innovation #Pharma "๐๐ก๐ ๐๐ซ๐ข๐๐ ๐ ๐๐๐ญ๐ฐ๐๐๐ง ๐ ๐๐% ๐๐๐ข๐ฅ๐ฎ๐ซ๐ ๐ซ๐๐ญ๐ ๐๐ง๐ ๐๐ฅ๐ข๐ง๐ข๐๐๐ฅ ๐๐๐ซ๐ญ๐๐ข๐ง๐ญ๐ฒ ๐ข๐ฌ๐ง'๐ญ ๐ฃ๐ฎ๐ฌ๐ญ ๐ ๐ง๐๐ฐ ๐ญ๐จ๐จ๐ฅโ๐ข๐ญ'๐ฌ ๐ ๐ง๐๐ฐ ๐ฌ๐ญ๐๐ง๐๐๐ซ๐."