Insights On Pharmaceutical Packaging
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A Risk-Based Approach To Injectable Combination Product Development
3/14/2023
Examine how to establish a holistic approach to drug-device combination product (DDCP) development and how to assess and manage risk throughout the development and approval process.
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Stability Chambers: Testing, Equipment, And Uses
3/7/2023
Performing stability studies is a critical step in the drug development process. Discover the ways to ensure that your drug is safe and effective as it goes to market.
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Semi-Solid And Semi-Liquid Dosage Forms: What To Know
3/7/2023
Interest in semi-solid dose (SSD) forms has been on the rise. Learn more about the advantages of formulating medications into SSD forms as well as the challenges to consider.
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Lyophilization Contract Manufacturing Services: What To Know
3/7/2023
Explore the best ways to optimize your lyophilization cycle and the benefits of partnering with an experienced pharmaceutical contract manufacturing services provider.
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Meeting The Growing Demand For Pre-Filled Syringes
3/7/2023
The market for pre-filled syringes is growing rapidly. Learn more about the benefits for consumers, providers, and manufacturers, and the importance of partnering with a reliable fill finish facility.
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Transitioning From A Vial To PFS Or Cartridge In An Auto-Injector Device
12/2/2022
Explore how to approach the transition of migrating from a vial to a syringe or cartridge, the necessary compatibility testing, and the stresses on the bulk product during formulation and filling.
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Keys To Successful Blinded Labeling
11/15/2022
The content and creation of blinded labels are tightly regulated and benefit from the guidance of an experienced partner.
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Evaluation And Management Of Vendor-Qualified Thermal Solutions
10/27/2022
Evaluating vendor qualification of thermal solutions is necessary due diligence in an industry where risk guides nearly all decision-making, as well as many regulatory mandates.
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Inside An Onsite Test Lab
10/13/2022
Learn about the extensive testing and validation to ensure product performance based on risk assessments performed under CPC’s ISO 13485 quality system, streamlining approval processes and allowing manufacturers to reach market faster and with less work.
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Planning Your Packaging For A Seamless Transition From Clinic To Launch
7/19/2022
Explore how clinical and commercial teams should work together for clinical supply packaging, how the COVID-19 pandemic has changed things, and what to consider when looking for a packaging partner.