The Role of AI in Quality Systems for Pharma, Now and in the Future

AI is poised to revolutionize how pharma companies approach quality management, from automating routine tasks to enhancing data accuracy and compliance. AI-driven tools can streamline processes, reduce human error, and provide predictive insights that improve decision-making. As the industry continues to evolve, understanding AI's role in quality systems is essential for staying ahead in an increasingly competitive market.

We see three stages of AI adoption in quality systems and software for the pharmaceutical industry:

1. Conversational Information Retrieval
2. Identifying Patterns and Correlations
3. Predictive Analytics

The potential impact of AI on quality systems in pharmaceutical companies is dramatic and evolving rapidly, but we have a clear vision of how to leverage AI in quality systems in the near term.

At Scigeniq, we are well down the path to integrating these advanced AI capabilities into our products. As we continue to innovate and develop our SaaS product suite, our plans and product roadmap will no doubt evolve because AI capabilities are evolving as fast as we can integrate them.

Learn more here.

Navigating ANVISA and The Unique Regulatory Environment in Brazil

This month, we also explored the complexities of navigating ANVISA, Brazil's National Health Surveillance Agency, and its unique regulatory environment. We highlight the distinct challenges that pharmaceutical companies face when seeking market approval in Brazil, including understanding ANVISA's stringent requirements and adapting to its regulatory framework.

We also offer insights into best practices for achieving compliance, emphasizing the importance of thorough preparation, local expertise, and staying updated with regulatory changes. Successfully navigating ANVISA's processes is crucial for pharmaceutical companies looking to enter and thrive in the Brazilian market.

Check out the full blog.

Customer Story: Globalpharma

Globalpharma, a leading generic pharmaceutical manufacturer in the GCC, partnered with Scigeniq to enhance its regulatory and document management processes.

• Regulatory Management Transformation: Implemented Scigeniq's RMS to replace Excel spreadsheets, improving data management and reporting.
• Document Automation: Adopted Scigeniq's DMS, automating document processes, integrating with SAP for batch number generation, and migrating 2,000 documents.

By implementing Scigeniq's Regulatory Management System (RMS) and Document Management System (DMS), Globalpharma streamlined data management, improved reporting, and automated document workflows.

The collaboration was marked by strong support from Scigeniq's experienced team, enabling GlobalPharma to overcome challenges and plan for future integrations.

Read their story.

Upcoming Events

Just a reminder of where we'll be in the fall.

• InnoPharma Conference in Campinas, S?o Paulo - September 12, 2024, COO, Wagner Moi will present. He'll discuss the value AI brings to operations software.
• CPHI - December 10-12, find us at Booth 3, C5. Drop by to chat or get a demo of one of our solutions. If you'd like to set up a meeting, reach out, and we'll schedule a time.

About Scigeniq

We are deeply committed to helping customers leverage world-class software solutions to drive dramatic improvements in quality, regulatory, and content-management processes. Check out our full suite of quality, training, document management, and regulatory solutions to automate and optimize end-to-end processes and deliver maximum impact. With decades of experience with some of the largest and best-known pharma companies in the Middle East and Africa, Brazil, and South America, we work hard to bring best practices and a pragmatic perspective to every customer’s implementation of their solutions.

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