Team Name | Nupeak Pioneers |
Track |
Healthcare and Life Sciences |
Use Case |
In the pharmaceutical industry, manufacturing processes play a crucial role to ensure the production of safe and effective medications. The formulation and manufacturing of pharmaceutical products involve complex procedures, with numerous variables that can impact product quality. A critical aspect of this process is achieving consistency in product quality and efficacy batch after batch. This is where Golden Batch analysis plays a pivotal role. A Golden Batch is characterized as "the chronological sequence of measured values obtained from a specific batch that achieved quality standards." Essentially, it serves as a method to pinpoint an optimal output and enhance the manufacturing procedures to recreate the circumstances leading to its attainment. Subsequently, they can adjust and fine-tune their manufacturing processes to replicate these conditions consistently. This not only ensures the production of high-quality medications but also helps in maintaining regulatory compliance and meeting stringent industry standards. Ultimately, Golden Batch analysis serves as a crucial tool for pharmaceutical manufacturers in their pursuit of consistent product quality, safety, and efficacy. |
Technology | SAS Viya, SAS Visual Analytics, SAS Model Manager |
Region | India, Asia Pacific |
Team lead | Manish Bajpai |
Team members | @Dimplegoswami @avantikabhosale @manish_bajpai |
Social media handles | NA |
Is your team interested in participating in an interview? | Y |
Optional: Expand on your technology expertise | NA |
Pitch video
Jury Video
The Golden Batch Analysis Solution is highly valuable for ensuring cGMP (current Good Manufacturing Practices) compliance in the pharmaceutical industry. By leveraging advanced data analytics and historical performance data, it enables manufacturers to identify optimal production conditions and improve batch consistency. This approach enhances process understanding, reduces variability, and minimizes the risk of deviations, ultimately leading to higher product quality and safety. Additionally, it supports continuous improvement initiatives and regulatory compliance, making it an essential tool for pharmaceutical manufacturers striving for operational excellence.
Join us for SAS Innovate 2025, our biggest and most exciting global event of the year, in Orlando, FL, from May 6-9.
Early bird rate extended! Save $200 when you sign up by March 31.
Build your skills. Make connections. Enjoy creative freedom. Maybe change the world. Join us at the 2025 SAS Hackathon Sept. 15 – Oct 10. Visit the SAS Hackathon homepage.
Check it out!