Choosing a drug manufacturing site based on a product's point in the life cycle benefits patients, first by enabling rapid, reliable access to new therapeutics, and later by driving down the cost of mature products.
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In the initial days of integrated services, CDMOs were primarily geared toward early-stage development, helping clients obtain an investigational new drug (IND) application. Today, however, integrated CDMOs like Piramal Pharma Solutions assist companies across the entire development process, including late stage and commercial projects.
From discovery to intermediates, active pharmaceutical ingredients (APIs) and drug products, a CDMO requires expertise across multiple elements of the pharma process to deliver an integrated experience. Through comprehensive project management teams, PPS oversees and executes all elements of this work on behalf of its clients and their patients. By taking ownership of the end-to-end integrated project, we gain in speed while also de-risking transfers between multiple CDMOs.
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Other Available Whitepapers
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Deploying Bioavailability Enhancement Techniques to Improve Patients' Lives
Oral bioavailability is a constant challenge for developers of new chemical entities. Low solubility and permeability often reduce the fraction of an orally administered drug absorbed in the bloodstream. Increasing the dose to have adequate circulating drug at the intended site of action may not always be a feasible option. As such, drug developers need ways to improve the bioavailability of their molecules.
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Eastern & Western Manufacturig Solutions for Late Life Cycle Products
Choosing a drug manufacturing site based on a product's point in the life cycle benefits patients, first by enabling rapid, reliable access to new therapeutics, and later by driving down the cost of mature products. The challenge is to find production sites that cater to both the specific priorities faced at different points in the life cycle and the universal requirements that apply to all products at all times.
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