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1849 E. 1450 Rd. , Lawrence, KS, 66044, US
CritiTech is a multi-service CDMO specializing in pre-formulation, formulation, particle engineering, analytical methods and testing, and preclinical to GMP manufacturing. We use spray drying, jet milling and our proprietary Purcision platform to engineer non-cyto, cyto, potent, and inhaled drugs. CritiTech produces fast, impactful and quality results.
The Future of Oral Solids explores how innovation, advanced manufacturing, and integrated CDMO partnerships are reshaping the oral solid dosage (OSD) landscape, now and in the years ahead.
Released By Adare Pharma Solutions
Codis launches as a global CDMO specializing in spray drying, amorphous solid dispersions, and particle engineering, uniting Particle Dynamics and EUROAPI’s former Haverhill facility under one brand.
Released By Codis
Sentry’s foreign trade zone expertise helps pharmaceutical companies mitigate risks from tariffs and global trade volatility.
Released By Sentry BioPharma Services, Inc.
AGC Biologics to provide GMP manufacturing for AAVantgarde’s two novel candidates designed to address progressive and irreversible vision loss.
By: Charlie Sternberg
Underscores the facility’s dedication to upholding the highest standards of quality across operations.
A conversation with Upperton’s Director of Pharmaceutical Sciences
Released By Upperton
The collaboration will leverage AGC Biologics' mRNA manufacturing knowledge and expertise to combat a leading cause of human mortality.
Non-exclusive license provides Solid’s proprietary, next-gen capsid, AAV-SLB101, to Andelyn Biosciences.
Over the past 20 years, the company has grown from a small startup into a trusted CDMO partner for biopharma companies worldwide.
A guide to the advantages and disadvantages of One-site vs Multi-site/Global CDMOs
Lessons Learned and Best Practices from a CDMO Perspective
Ji will drive strategic planning, operations, and the continued expansion of the company’s development and manufacturing capabilities.
By: Kristin Brooks
Stewart will lead integration of technology and process transformation initiatives across Avid's development and manufacturing network.
The Challenge of Adapting to Shifting Requirements
Released By ROIS CDMO
Hancock is a biotechnology executive with more than 40 years of leadership experience in CDMOs and pharmaceutical development companies.
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