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2023 Nice Insight Reports
Cell & Gene Therapy: 2023 Market Analysis, CDMO Pricing and Benchmarking
Monoclonal Antibody & Recombinant Protein: 2023 Market Analysis, CDMO Pricing and Benchmarking
mRNA Vaccines & Therapeutics: 2023 Market Analysis, CDMO Pricing and Benchmarking
Sterile Drug Product: 2023 Market Analysis, CDMO Pricing and Benchmarking
Active Pharmaceutical Ingredients: 2023 Market Analysis, CDMO Pricing and Benchmarking
Antibody Drug Conjugates: 2023 Market Analysis, CDMO Pricing and Benchmarking
Contract Research Organizations: 2023 Market Analysis, Pricing and Benchmarking
Oral Solid Dosage: 2023 Market Analysis, CDMO Pricing and Benchmarking
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Process Development
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Biocatalysis
Olon Presents the First Results Announcing to Have Achieved Developing A New Production Process Through Engineering Target Enzyme
PR-M05-23-02
Sustainable Manufacturing
Sustainability in Pharmaceutical Manufacturing: A CDMO’s Contribution
PAO-11-022-CL-07
Multispecific Antibodies
Optimized Multispecific Antibody Design, Development, and Manufacturing
PAO-08-022-CL-04
Capacity Expansion
Avid Bioservices Announces Further Expansion of Process Development Capacity for Mammalian Cell Business
PR-M06-22-02
R&D
Driving Further Innovation by Integrating a Decentralized R&D Network
PAO-06-022-CL-02
Advanced Excipients
How the Developability Classification System and Advanced Excipients Enable the Formulation of Poorly Soluble APIs
PAO-04-022-CL-07
Mesenchymal Stem Cells
A Media Platform for Cost-Effective and Scalable 2D and 3D Bioreactor MSC Expansion
PAO-04-022-CL-05
Aseptic Processing
Unique Manufacturing Challenges Associated with Sterile Eye Ointments
PAO-04-022-CL-04
Vaccine and Cell & Gene Therapies
Expanding Manufacturing Capacity to Meet Market Demand for Vaccines and Cell and Gene Therapeutics
PAO-04-022-CL-02
Process Validation
Streamlining Process Validation for Drug Substance Manufacturing
PAO-02-022-CL-19
Oncolytic Viruses
Best Practices For Oncolytic Virus Design, Development, and Manufacturing
PAO-02-022-CL-17
Manufacturing Authorization
Vetter’s New Clinical Manufacturing Site Now Officially Authorized
PR-M01-22-12
mRNA
Integrated Support Facilitates mRNA Product Development and Commercialization
PAO-10-21-CL-15
Process Development
Designing More Sustainable Small Molecule API Manufacturing Processes
PAO-09-21-CL-05
Cell and Gene Therapy
6 Analytical Strategies to Consider Before Submitting Your Cell and Gene Therapy Application
PAO-06-21-CL-04
Synthetic Biology
An Unnatural Phenomenon: How Synthetic Biology May Disrupt Pharma and Beyond
PAO-06-21-NI-02
Gene Therapy
Avoiding Costly And Time-Consuming Mistakes In Gene Therapy Process Development
PAO-03-21-CL-08
Chemistry, Manufacturing, and Controls
Phase-Appropriate CMC Activities Facilitate the Transition from Early Development through Commercialization
PAO-01-21-CL-05
Process Development
Innovative Approach to Process Development
PAO-02-21-CL-02
Analytical Development
Solving Process Challenges Requires Flexibility to Explore Alternative Analytical Methods
PAP-Q4-19-CL-017
Translational Pharmaceutics
Measuring the Time and Cost Benefits of Integrated Product Development
PAP-Q4-19-CL-017
Strategic Partnership
Partnering for Success from Concept to Commercialization
PAP-Q4-19-CL-010
Capacity Expansion
Biotechpharma to Expand Process Development and GMP Manufacturing Capacity to 5,000 L
PR-M04-19-NI-057
Process Development
Overcoming Challenges in Microbial Process Development
PAP-Q1-2019-CL-010
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