Explore recent issues of Contract Pharma covering key industry trends.
Read the full digital version of our magazine online.
Behind every facility expansion, technology investment, and quality milestone in the CDMO sector is a leadership team making deliberate choices about where to focus, how to grow, and when to take calculated risks.
Stay informed! Subscribe to Contract Pharma for industry news and analysis.
Get the latest updates and breaking news from the pharmaceutical and biopharmaceutical industry.
Discover the newest partnerships and collaborations within the pharma sector.
Keep track of key executive moves and promotions in the pharma and biopharma industry.
Updates on the latest clinical trials and regulatory filings.
Stay informed with the latest financial reports and updates in the pharma industry.
A video roundup of the week’s top industry news stories.
Expert Q&A sessions addressing crucial topics in the pharmaceutical and biopharmaceutical world.
In-depth articles and features covering critical industry developments.
Access exclusive industry insights, interviews, and in-depth analysis.
Insights and analysis from industry experts on current pharma issues.
A one-on-one video interview between our editorial teams and industry leaders.
Listen to expert discussions and interviews in pharma and biopharma.
Contract Pharma Stream offers a centralized destination where users can watch expert-led sessions anytime, anywhere
A detailed look at the leading US players in the global pharmaceutical and BioPharmaceutical industry.
Browse companies involved in pharmaceutical manufacturing and services.
Comprehensive company profiles featuring overviews, key statistics, services, and contact details.
A comprehensive glossary of terms used in the pharmaceutical and biopharmaceutical industry.
Watch in-depth videos featuring industry insights and developments.
Download in-depth eBooks covering various aspects of the pharma industry.
Access detailed whitepapers offering analysis on industry topics.
View and download brochures from companies in the pharmaceutical sector.
Explore content sponsored by industry leaders, providing valuable insights.
Stay updated with the latest press releases from pharma and biopharma companies.
Explore top companies showcasing innovative pharma solutions.
Meet the leaders driving innovation and collaboration.
Engage with sessions and panels on pharma’s key trends.
Hear from experts shaping the pharmaceutical industry.
Join online webinars discussing critical industry topics and trends.
A comprehensive calendar of key industry events around the globe.
Live coverage and updates from major pharma and biopharma shows.
Find advertising opportunities to reach your target audience with Contract Pharma.
Review the editorial standards and guidelines for content published on our site.
Understand how Contract Pharma handles your personal data.
View the terms and conditions for using the Contract Pharma website.
What are you searching for?
Aims to provide a coordinated pathway to bring clinical and commercial gene therapy materials from the U.S. into the EU and the UK.
October 8, 2026
By: Kristin Brooks
Editor’s take: With the increasing complexity of CGT programs, sponsors are focusing on strategic partnerships to expand their offerings.
Andelyn Biosciences, a US-based cell and gene therapy CDMO, and PQP Group entered a strategic partnership to expand support for sponsors supplying cell and gene therapy products to clinical sites in the EU and UK. PQP, headquartered in the UK and the Netherlands, holds Manufacturing and Import Authorizations and provides Qualified Person (QP) services that enable clients to import and release medicinal products from outside these territories, supporting Clinical Trial Authorizations (CTAs) and related supply.
The relationship establishes a standard process to support sponsors in these regions. Andelyn and PQP have completed foundational work designed to enable an efficient and well-defined process for clients and sponsors.
This framework integrates Andelyn’s development, manufacturing, quality, and supply chain capabilities with PQP’s services, including QP audit reports, QP declarations, Product Specification File (PSF)creation, Investigational Medicinal Product Dossier (IMPD) and batch review, batch certification, import and shipping services (importer of record, broker, import license, and depot storage), and distribution support.
Together, Andelyn and PQP aim to provide sponsors with a more coordinated pathway to bring clinical and commercial gene therapy materials from the U.S. into the EU and the UK.
“Expanding access to reliable clinical supply pathways is an important step toward helping our clients advance life-changing cell and gene therapies globally,” said Matt Niloff, CCO at Andelyn. “Through this relationship with PQP Group, we are supporting sponsors with an integrated approach that combines Andelyn’s manufacturing and quality capabilities with specialized EU and UK QP, import, and distribution expertise.”
“PQP is pleased to partner with Andelyn to provide a coordinated clinical supply offering for sponsors advancing innovative therapies into the EU and UK,” said Stephan Croft, Co-founder and QP at PQP Group. “By combining Andelyn’s established cell and gene therapy manufacturing capabilities with PQP’s QP and regional supply-chain expertise, we are helping sponsors navigate critical steps in importing, certifying, and delivering clinical material.”
Get the latest Contract Pharma news, insights and analysis in your Google Search and AI experiences.
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !