The Role of Technology and Automation in Contract Manufacturing
Being a successful contract pharmaceutical manufacturer means being able to ensure that a number of operations ranging from sourcing to manufacturing to quality check to storage and supplying the shipment to the clients take place efficiently one after the other or even simultaneously. To do all of this in a...
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Bridging the Demand-Manufacturing Gap in the Growing Large Volume Parenteral (LVP) Market: The Role of CDMOs
There is a rise in the demand for large-volume parenterals (LVPs) due to an increase in the number of surgeries and people requiring frequent hospitalizations due to chronic diseases. As opposed to the climbing interest in LVP, pharma companies are unable to cater to this burgeoning demand as very...
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Addressing Global Health Disparities: Access to Medications
Health disparities are discrepancies that socially disadvantaged populations face with respect to the burden of disease, injury, violence, or opportunity to reach optimal health. These differences are preventable. They occur due to a plethora of factors. These include but are not limited to poverty, environmental threats, individual and behavioral...
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June 8, 2023
| Pharmaceuticals
How can companies benefit from integrating contract manufacturing in pharma in early-stage drug development and manufacturing projects?
Contract manufacturing in pharma Contract manufacturing in pharma refers to the outsourcing of the production of pharmaceutical products to specialized companies that have the expertise and equipment to manufacture them known to be pharmaceutical contract manufacturing organizations (CMOs) or contract development and manufacturing organizations (CDMOs). By outsourcing to...
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Find the pharma contract manufacturer for Sterile Fill-Finish in ampoules for Complex Drug Products.
An Introduction Sterile fill-finish in ampoules for complex drug products refers to the process of filling and sealing pre-sterilized glass vials, known as ampoules, with complex drugs that require special handling or contain sensitive or biologically active ingredients. The process involves rigorous quality controls to ensure that the...
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Role of CDMOs in Enhancing Syrup Formulations Taste for better patient acceptability
Taste & Syrup Formulations Enhancing syrup formulations' taste for better patient acceptability is required because the taste is an important factor in medication adherence. When a medication tastes unpleasant, patients are less likely to take it as prescribed, leading to poor treatment outcomes. Improving the taste of syrup...
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Unlock the Potential of Twist-Off Capsules for Precise Dosing and Versatile Formulations with a Leading Pharmaceutical Contract Manufacturer
Pharmaceutical contract manufacturers The pharmaceutical sector is known for its consistency, accuracy, and reliability. The same is maintained in all its endeavors. Pharmaceutical contract manufacturers have made this more acceptable with their able support and skilled competencies which helped the pharma companies to come up with the latest...
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CDMO Explore the Potential of Mouth Melt Powder for better patient compliance
CDMOs and Mouth Melt Powder CDMOs (Contract Development and Manufacturing Organizations) are continuously exploring innovative dosage forms to improve drug delivery and patient compliance. The mouth melt powder is one such innovative dosage form designed to provide a convenient and palatable option for patients who have trouble swallowing...
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Finding the best CDMO for enhancing the permeation of gel formulations for better pain management
Permeation of gel formulations: An Introduction Permeation refers to the process by which a substance moves through a barrier, such as skin or a membrane. In the context of gel formulations, permeation refers to the ability of the gel to penetrate the skin or other tissues and deliver...
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The Pharma Third Party Manufacturing site should be capable of assisting in early-stage process development for both API and finished drug products.
Active Pharmaceutical Ingredient (API) API stands for "Active Pharmaceutical Ingredient," is the part of a drug that produces the intended pharmacological effect and is responsible for the therapeutic activity of a medication. Simply, the API is the chemical substance that is responsible for treating a specific condition...
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