INSIGHTS ON PHARMACEUTICAL LOGISTICS
-
Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics
Join this roundtable of biopharmaceutical professionals as they share their insights to help you navigate important quality and planning decisions for the progression of your biologic.
-
Integrated Single-Site CDMO Model
A single‑site model reduces handoff risks, speeds timelines, strengthens quality oversight, and unifies development and manufacturing to improve reliability and execution efficiency.
-
Global Strategies For Resilience And Redundancy In Cell Culture Media Supply
Ensure your cell culture media supply remains uninterrupted. Explore proactive strategies for global manufacturing equivalency and consistent media delivery.
-
Accelerating Cold Chain Expansion: Responding To COVID-19 Challenges
Review how leveraging cross-functional teamwork helped complete a cold chain infrastructure expansion in a fraction of the expected timeline, ensuring the production of essential COVID-19 therapeutics.
-
Embracing Digital Transformation In Life Science Manufacturing: A Path To Excellence1/13/2025
Discover how life science manufacturers are supported in digital transformation, offering solutions for automation, data integration, and compliance to optimize operations.
-
Strengthen Pharmaceutical Supply Chains With A U.S.-Based CDMO6/5/2025
While certain ingredients require sourcing abroad, partnering with a U.S.-based company that owns its manufacturing assets allows for direct oversight of product quality and supply reliability.
-
Biopharma Supply, Reimagined: Regional, Resilient Manufacturing4/1/2026
Persistent disruption is redefining biopharma supply chains. Explore how regional manufacturing, integrated risk management, and closer collaboration help build resilience and improve agility.
-
Building A Resilient Supply Chain For Your Next-Generation Peptide Therapeutic1/23/2025
As peptide therapeutics continue to establish themselves as a leading technology for treating chronic indications, drug sponsors must identify reliable peptide building block suppliers to secure high-quality starting materials.
-
Biopharma Supply, Reimagined: Blarney, A Climate-Neutral Facility For Best-In-Class Filters11/11/2025
Explore how a new, climate-neutral manufacturing facility strengthens biopharma supply chains. Understand the benefits of its advanced filtration technologies and commitment to environmental sustainability.
PHARMACEUTICAL LOGISTICS SOLUTIONS
-
The counterfeiting of pharmaceutical products is one of the most significant tasks facing pharmaceutical packaging companies. Discover consulting for your supply chain that ensures compliance and enhances traceability.
-
Ropack's portfolio of primary pharmaceutical packaging methods meets the highest quality and safety standards.
-
Used VWR ULT freezer, model 5706, capable of -80 C temperatures, R-404a, R-508b refrigerant, 2 stage operation, with chart recorder and controls, (4) shelves, 208/230 volts, serial# 833437-852, built 2013.
-
Ropack offers a number of pouch and sachet filling services for powder, solid, liquid, and other dosage types.
-
SoftMax® Pro Software - The most published microplate reader control and data analysis software
Preconfigured protocols and custom assay workflows simplify microplate data acquisition and analysis
SoftMax® Pro Software for Windows 10 is designed to provide the simplicity, flexibility and power required for advanced data analysis. It provides ready-to-run protocols, analysis algorithms, and 21 different curve fit options. Every step is optimized for data acquired from a Molecular Devices microplate reader or data imported from another source to simplify analysis and reporting. Compliance tools are available for regulated laboratories providing end-to-end chain of custody.