Displaying 1–2 of 2 results for Fill & Finish

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Where and What to Test: From Purified Bulk Drug Substance to Sterile Liquid ...

(Whitepaper)

This white paper focuses on what many consider the most critical part of a biological drug product’s manufacturing life cycle: going from the purified bulk drug substance (“PBDS”) to the sterile final drug product (“FDP”). Specifically, the white paper discusses establishing the testing “where ...

Selecting An Aseptic Fill/Finish Contract Manufacturer: Avoiding the Most ...

(Whitepaper)

Selecting and establishing an effective working relationship with an Aseptic Fill/Finish contract manufacturer can be a challenging task. The ramifications of making a poor decision can result in schedule delays, regulatory approval issues, and lost revenue.This white paper provides guidance on ...

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