Logistics

INSIGHTS ON PHARMACEUTICAL LOGISTICS

Outsourcing To ISO 17025 Accredited Suppliers
Discover the advantages of outsourcing equipment calibration to ISO 17025 accredited suppliers, including cost efficiency and regulatory assurance, in our detailed analysis. Read more to transform your calibration processes.
A Temperature-Stable Replacement For Animal Trypsin In Cell Dissociation Applications
Improve cell dissociation with a gentle, recombinant enzyme. This temperature-stable protease shows dissociation kinetics similar to porcine trypsin but with lower cell toxicity and greater overall purity.
Building A Resilient Supply Chain For Your Next-Generation Peptide Therapeutic
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.
Windsor Framework: What Is It?
Learn about the Windsor Framework and how it addresses the challenges of medicine supply chains between the UK and the EU, creating stability and certainty in the post-Brexit world.

Strengthen Pharmaceutical Supply Chains With A U.S.-Based CDMO
6/5/2025

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.
5 Signs You've Outgrown Your Quality Management System (QMS)
12/27/2024

An outdated QMS limits growth. Explore how upgrading to an advanced, configurable system like MasterControl can ensure scalability, automation and innovation.
Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics
1/22/2025

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.
Optimized Processes: A Guide To Lyophilization Cycle Development
6/25/2024

Review the essential phases of the lyophilization cycle — freezing, primary drying, and secondary drying — and critical success factors to achieve optimal product quality and stability.
Accelerating Cold Chain Expansion: Responding To COVID-19 Challenges
8/21/2024

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.

Contract Manufacturing Of Devices

We offer a broad range of manufacturing services and capabilities to produce high-quality devices including pen-injectors, auto-injectors, and wearables.
Transport Solutions To Boost Your Line Efficiency

How can you safely transport masses of delicate syringes along production lines at a speed that benefits your business? What about all your specific product requirements? Our cutting-edge overhead conveying, lane management, accumulator and buffer solutions are scalable and adaptable – and we handle all your products with care.
Solid Dose Pharmaceutical Contract Packaging Capacities

Hard work is just part of the Ropack ethos, and we prove it daily through our output: high-capacity turnover that does not compromise our quality or excellence. All estimates based on three six-hour shifts per day.
Pharmaceutical Clinical Trial Distribution Services

Contracting an in-country pharmaceutical clinical depot brings efficiencies to your clinical trial distribution. From its facilities in Montreal, Quebec, Ropack handles most paperwork, permissions, components, warehousing, packaging, distribution, collection, and destruction as a single project.
PCI Clinical Trial Services

PCI is committed to supporting clients at every stage of the clinical cycle, delivering best-in-class services efficiently and effectively. We deliver a seamless clinical service including pharmaceutical development, clinical manufacturing, labeling, storage and distribution.