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Grifols
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New CDMO Facility
Leveraging a State-of-the-Art CDMO Facility to Advance Healthcare
PAO-02-23-PATV-04
Parenteral Drug Products
Innovating to Optimize Quality in Injectable Drugs
PAO-11-022-CL-16
Alzheimer's Vaccine
Araclon Biotech Advances in Its Innovative Vaccine and Diagnostic Test for Alzheimer's
PR-M03-22-06
Parenteral Manufacturing
Staying Ahead of Trends in Small-Volume Parenteral Manufacturing
PAO-01-22-R250-08
Recombinant Proteins
Meeting the Renewed Demand for Microbial Protein Production
PAO-01-22-R250-07
Parenteral Drugs
A CDMO Dedicated to Supporting Small-Volume, Small-Molecule Parenteral Projects
PAO-12-21-CL-02
Hyperimmunes
GigaGen Publishes Research on Company’s Recombinant Hyperimmunes in Nature Biotechnology
PR-M04-21-018
Acquisition
Grifols Reinforces its Innovation Strategy After Completing the Acquisition of GigaGen to Boost a Novel Method to Generate a Wide Range of Immunoglobulins
PR-M11-20-045
Parenterals
Trends Shaping the Dynamic Market for Parenterals
PAP-Q3-20-CL-018
Continuous Improvement
The Critical Role of Continuous Improvement in Parenteral Drug Manufacturing
PAP-Q1-20-CL-010
M&A
Aradigm Announces Entering into an Asset Purchase Agreement with Grifols, S.A.
PR-M02-20-NI-031
Orphan Drugs
Customer Engagement and Information Sharing are Essential for Success in Orphan Drug Outsourcing
PAP-Q3-19-CL-013
FDA Approval
Grifols Announces FDA Approval of Xembify®, 20% Subcutaneous Immunoglobulin for Primary Immunodeficiencies
PR-M07-19-NI-018
Parenteral Manufacturing
Catering to a Growing Demand for Small-Volume Parenteral Manufacturing
PAO-M04-19-CL-001
Parenteral Solutions
Supporting Small and Emerging Pharma through Collaboration and Specialized Expertise
PAP-Q2-2019-CL-017
Form-Fill-Seal
Investing in Form-Fill-Seal Technology
PAP-Q1-2019-CL-011
Facility Opening
Grifols Announces the Opening of its new Plasma Donor Center in Russellville, AR
PR-M03-19-NI-082
FDA Approval
Grifols Receives FDA Approval for Procleix Babesia Assay for Donor Screening on Procleix Panther System
PR-M02-19-NI-017
Quality
Continuous Quality is Essential in Parenteral Manufacturing
PAO-M12-18-CL-003
FDA Approval
FDA Approves Grifols ID CORE XT Test For Molecular Red Blood Cell Typing
PR-M10-18-NI-047
Terminal Sterilization
Terminal Sterilization for Parenteral Drugs: Finding the Right CDMO Partner
PAP-Q3-18-CL-015
FDA Approval
Grifols Achieves Key Milestone with FDA Approval of the New Consolidated Manufacturing Facility (CMF) for Production of Recombinant Proteins
PR-M08-18-NI-123
Parenterals
A Risk Analysis Approach to Producing Environmentally Sensitive Parenterals
PA0-M06-18-CL-007
FDA Approval
Grifols Expands its NAT Solutions Portfolio with New FDA Approvals for Two Assays
PR-M06-18-NI-064
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