Outsourcing to a CDMO can significantly reduce operational costs and increase efficiency. By partnering with Lannett CDMO, companies can leverage our expertise and infrastructure, allowing them to focus on their core competencies.

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#PharmaOutsourcing #OperationalEfficiency #CostReduction
#PharmaceuticalManufacturing #BusinessPartnership #Lannett #lannettcdmo

Accelerate Your Drug to Market. Overcome development challenges and speed up your launch with a good CDMO partnership. Discover how a CDMO partnership can help overcome development challenges and speed up market launch.

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Enhancing Efficiency and Resilience in Pharmaceutical Supply Chain Management
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The Importance of Quality Assurance in the Pharmaceutical Industry
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Navigating the Complex World of Pharmaceutical Regulatory Support
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Behind every pill lies meticulous precision and unwavering commitment to quality. Welcome to the heart of pharmaceutical manufacturing.

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Lannett CDMO is established on a long history of excellence, quality, and trust. When we work with you, we ensure that your product gets the attention and care it deserves from concept to delivery. For 75 years, we have maintained this level of commitment with our partners, and will continue to do so for as long as we are able.

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#excellence #quality #commitment #cdmo #CellTherapyManufacturingMarket

Understanding Pharmaceutical Supply Chain Management: A Comprehensive Guide

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Effective #SupplyChainManagement ensures seamless operations and secure delivery of high-quality products to patients. From sourcing raw materials to distribution, our meticulous approach guarantees reliability and efficiency at every step. We can help you strategically navigate the complexities of supply chain management.
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Lannett CDMO utilizes wet high-shear granulation. This is when a liquid binder is added to the powder mixture to form granules. This process can be used for producing:

Tablets: For granules with good flow properties and compressibility.
Capsules: For uniformity and flowability for capsule filling.
Controlled Release: For specific release profiles with set parameters and properties.

Got a particular Oral Solid Dosage form in mind? Talk to us to find out more.

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Lannett’s laboratories are well-equipped and spacious; our walk-in and reach-in stability chambers can be validated at a variety of conditions, the common being:

- Long-term (25°C and 60%RH or 25°C and 40%RH)
- Intermediate (30°C and 65% RH)
- Accelerated (40°C and 75%RH or 40°C and 25%RH)

Our laboratory capabilities are all about providing solutions fitted to your needs.

https://www.lannettcdmo.co...

Lannett’s laboratories are well-equipped and spacious; our walk-in and reach-in stability chambers can be validated at a variety of conditions, the common being:

- Long-term (25°C and 60%RH or 25°C and 40%RH)
- Intermediate (30°C and 65% RH)
- Accelerated (40°C and 75%RH or 40°C and 25%RH)

Our laboratory capabilities are all about providing solutions fitted to your needs.

https://www.lannettcdmo.co...

High-shear granulators are specialized equipment particularly used for producing oral solid dosage forms like tablets. These machines combine blending and granulation in one process, making them highly efficient for producing uniform granules. Thanks to advanced machines like these, Lannett CDMO is able to achieve high product yield rate and on-time delivery.

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#OralSolidDoses #Granulation #OnTimeDelivery #Lannett hashtag#LannettCDMO

Ensuring Excellence: The Role of Quality Management Systems in the Pharmaceutical Industry
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Supply chain management (SCM) is critical in the pharmaceutical industry, where the stakes are higher than in most other sectors.

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Analytical development is a crucial aspect of pharmaceutical and biotechnology industries. It encompasses the processes and methodologies involved in developing reliable, accurate, and reproducible analytical methods to assess the quality, safety, and efficacy of drug substances and products.
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The Art and Science of Formulation Development in Pharmaceuticals
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Regulatory agencies like the US Food and Drug Administration (FDA) set strict guidelines to ensure the safety and efficacy of drugs.
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Outsourcing for Efficiency: Exploring Contract Manufacturing in Pharmaceuticals
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The Digital Revolution in Pharma: How CDMOs are Embracing Tech for a Healthier Future
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In the dynamic landscape of pharmaceuticals, contract manufacturing plays a pivotal role in bringing innovative therapies to patients worldwide.

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Precision medicine is founded on the principle that each person's genetic makeup influences their susceptibility to diseases, their response to treatments, and their overall health outcomes. By analyzing an individual's genome, scientists can identify genetic variations that may predispose them to certain diseases or influence their response to specific medications. Armed with this knowledge, healthcare providers can tailor treatments to target the underlying molecular mechanisms of diseases, maximizing efficacy and minimizing side effects.

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CDMOs often have established quality systems and expertise in navigating the complex and evolving regulatory landscape in the pharmaceutical industry. This expertise is valuable for clients seeking to ensure compliance and a smooth regulatory pathway. If you have questions and needs in this area, give us a call. We're more than ready and willing to help you with regulatory compliance.

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Quality control (QC) in the pharmaceutical industry is a critical component of ensuring the safety, efficacy, and quality of pharmaceutical products.
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pharma contract manufacturing organizations play a vital role in driving innovation, enhancing efficiency, and advancing global healthcare. Through collaboration, expertise, and a relentless commitment to quality, CMOs empower pharmaceutical companies to bring life-saving medications to patients around the world. As the industry continues to evolve, the strategic partnership between pharmaceutical companies and CMOs will remain a cornerstone of success, driving innovation, and improving patient outcomes for years to come.

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