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Aenova is a leading global contract manufacturer and development service provider for the pharmaceutical and healthcare industries. As a one-stop shop, Aenova develops, produces and packages all common dosage forms, product groups and active ingredient classes of pharmaceuticals and dietary supplements for human and animal health.
The Pros and Cons of Developing and Manufacturing Softgel Capsules.
Released By Aenova Group
Faster time to market with a holistic approach.
Dick is an experienced operations executive with over 30 years of experience in project and line management.
By: Charlie Sternberg
This project could reduce costs in pharmaceutical development and manufacturing.
By: Rachel Klemovitch
In today’s high-stakes pharma environment, where supply chain risks, rising tariffs, and time-to-market pressures dominate, smart manufacturers are turning to a powerful but underused tool: Foreign Trade Zones (FTZs). Our latest eBook, Foreign Trade Zones in Pharma Manufacturing, reveals how FTZs are helping drug makers cut costs, streamline customs, and bring manufacturing back to U.S. soil—without compromising on quality or regulatory compliance. Whether you're a sponsor, CDMO, or supply chain leader, this guide offers insights to help you compete more efficiently in a volatile global market.
Released By Jubilant HollisterStier CMO
For this roundtable, Contract Pharma called upon thought leaders across the pharmaceutical services sector to address “3 Key Trends” impacting the CDMO industry in 2025 and beyond.
By: Tim Wright
Looking at key trends in outsourcing, manufacturing, and regulatory compliance.
The new expansion will feature modernized machinery for faster production and more capacity.
Gil Roth, President of the Pharma & Biopharma Outsourcing Association, shared his insights in the CPHI Annual Report 2024, highlighting the key challenges the outsourcing industry may face as it heads into 2025. This is an edited version of that report; please note that it was written prior to the 2024 U.S. elections.
By: Gil Roth
A conversation with the CEO and president of JHS about the company's continued growth and the emerging trends shaping the CDMO landscape.
Bryan O’Donnell, Head of Quality at Gaelic Laboratories, explains how to navigate GMP challenges to ensure your company produces the highest quality pharma products that optimize patient safety and drug efficacy.
Aims to revolutionize pharmaceutical manufacturing with focus on advanced aseptic processing technology.
By: Kristin Brooks
Navigating GMP challenges with Bryan O’Donnell, Head of Quality at Gaelic Laboratories.
Adds capacity, talent and capabilities to support the growing demands for monoclonal antibodies, cell and gene therapy and mRNA workflows.
Aims to address critical biopharma industry challenges.
Adapting to the changing pharmaceutical landscape, key highlights for attendees, and looking ahead at strategic plans for CPHI.
Massive overhaul in works to embed greener processes.
By: Soman Harachand
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