Newsletter | May 18, 2020

05.18.20 -- An Introduction To Quality Agreements For Pharmaceutical Outsourcing

Featured Editorial
Industry Insights
Solving The OOS Problem With Continuous Manufacturing

With continuous manufacturing, it is possible to monitor product quality continuously and make adjustments in real time to keep the product in spec.

Seven Strategies To Avoid Delays In Clinical Supply

Ensuring an adequate, timely, and quality supply of comparator product for clinical trials is critical, but clinical trial sponsors face several challenges in this endeavor. Delivery delays or under-projection of needed quantities could have a negative impact on timelines, budgets, and patients relying on new treatment options for unmet needs. In this article, learn seven strategies to help you avoid clinical supply delays.

Novel Uses For Oral Solid Doses Driving Life Cycle Management Strategies

With few potential blockbuster drugs in the pharma pipeline right now, drug companies are increasingly looking at other options to meet the needs of patients and increase revenue in the oral solid dosage arena.

Does Selecting A CDMO Based On Contract Price Really Save You Money?

Before you sign on the dotted line, do a little digging to unearth potential costs that could turn your development program into a cash-burning exercise.

Guidelines To Bring Your Biologic To Market: Are You Prepared?

Are you up to the task of bringing a biologic drug to market? Do you have a strategy and plan for moving forward? Here we explore this, from a biopharma process development and manufacturing perspective.

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