Understand Your Process: A Key To CMO Risk Mitigation

The global pharmaceutical industry outsourced an estimated $65 billion in drug manufacturing volume to contract manufacturing organizations (CMOs) in 2016, according to the research firm Mordor Intelligence. According to a December 2023 report, the sterile injectable drugs contract manufacturing outsourcing market is expected to exceed $24.2 billion in 2024. Pharmaceutical companies contract…

The Dating Game – Trust & Compatibility In Outsourcing Partnerships

When selecting a manufacturing outsourcing partner and outsourcing partnerships, it's essential to evaluate both trust and compatibility to navigate the complexities of the clinical trial pipeline effectively. Singota Solutions (Bloomington, Indiana CDMO) offers specialized aseptic manufacturing solutions (a small batch aseptic filler, aseptic filling, etc) that cater to early-phase clients.…

The Advantages Of A Cross-Functional Staff Model In Pharmaceutical Manufacturing

In the world of pharmaceutical manufacturing, Singota Solutions (Bloomington, Indiana CDMO) stands out by leveraging a cross-functional staffing model that spans sampling/dispensing, formulation, filling, and finishing. This approach is complemented by our small batch aseptic filler and comprehensive aseptic manufacturing solutions (including aseptic filling). Employees are cross-trained, allowing them to…

Systematic Approach To Early Phase Sterile Drug Product Technology Transfer

Initial scale-up of a sterile drug product manufacturing process (early phase) can present significant challenges and risks to new drug development timelines, budgets, product quality, and patient safety if not properly managed. At Singota Solutions (Bloomington, Indiana CDMO), our expertise in injectable formulation development, combined with our advanced aseptic manufacturing…

Real-Time Monitoring Of Pharmaceutical Shipments

In today’s technologically advanced world, real-time monitoring of pharmaceutical shipments is crucial. Ensuring the integrity of sensitive, high-value products requires strict adherence to procedures and policies. At Singota Solutions (Bloomington, Indiana CDMO), we excel in managing the complexities of the pharmaceutical supply chain. With our GMP compliant warehouse and expertise…

Creating A Streamlined Process For Establishing Mutual Confidentiality Disclosure Agreements With A CDMO

Navigating confidentiality disclosure agreements (CDAs) swiftly and effectively is essential for fostering trust and collaboration between clients and CDMOs in the pharmaceutical industry. With complexities such as disparities in templates and multi-party agreements, the process can be challenging. At Singota Solutions (Bloomington, Indiana CDMO), we leverage a combination of expertise…

5 Qualifying Questions To Evaluate Solution Providers For Temperature Controlled Shipping

In the realm of pharmaceutical logistics, navigating the complexities of temperature-controlled shipping requires more than just a refrigerated warehouse and trucks. Life sciences companies seeking solutions in this arena must scrutinize potential vendors' qualifications. From assessing physical assets like a small batch aseptic filler and aseptic manufacturing solutions to ensuring…

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