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Quality
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Cell and Gene Therapy
Quality and Regulatory Challenges Surrounding New Cell and Gene Therapy Products
PAO-09-21-CL-07
Customer Centricity
What to Look for When Choosing the Right CDMO
PAO-09-21-CL-02
Quality
The Future of the Delivery of Quality
PAO-07-21-CL-01
Client Service
Avara on Client Service and Innovation— We Make It. About You.
PAO-07-21-CL-07
Quality
Strong Quality Systems and Quality Culture Ensure Inspection-Ready Status
PAO-06-21-CL-12
Visual Inspection
Inspection of BFS Containers–Reaching New Heights of Performance with 13 Cameras
PAO-06-21-CL-07
Gene Therapy
Planning for Success, Addressing Quality Early for Gene Therapies
Quality
Quality and Compliance Ensures Business Sustainability for Avara Arecibo Clients
PAO-05-21-CL-04
Gene Therapy
Avoiding Costly And Time-Consuming Mistakes In Gene Therapy Process Development
PAO-03-21-CL-08
Nitrosamine
Supporting Drug Manufacturers with Emprove® Nitrosamine Declarations
PAO-02021-CL-05
Extractables & Leachables
Aiding Material Qualification and Risk Assessment for Single-Use Biomanufacturing
PAP-Q4-20-CL-015
Vaccine Distribution
Anticipating the Logistics of a COVID-19 Vaccination Effort
PAP-Q3-20-CL-010
Parenterals
Trends Shaping the Dynamic Market for Parenterals
PAP-Q3-20-CL-018
Bioanalysis
How Bioanalysis Supports the Development of New Cell and Gene Therapies
PAP-Q3-20-CL-012
Secure Validated Shipping
The Essentiality of Transportation to the Pharma Industry
PAP-Q2-20-CL-004
Integration
Creating Value through Best Practices Across a Global, Integrated Service Provider
PAP-Q2-20-CL-009
Quality
Impurity Identification in Small-Molecule APIs
PAO-01-20-CL-005
Quality Compliance
How a Quality Culture Contributes to Global Compliance
PAP-Q4-19-CL-007
Innovation
Creating a Global CDMO Focused on Quality, Innovation and Happiness
PAP-Q3-19-CL-028
Quality
The Link Between a Robust Company Culture and Quality
PAO-06-2019-CL-001
Sterile
Quality and Experience Crucial for Sterility Assurance
PAP-Q2-2019-CL-014
Outsourcing
Aligning the Outsourcing Relationship
PAP-Q1-2019-CL-006
Stem Cells
Statement by FDA on Efforts to Stop Stem Cell Clinics and Manufacturers from Marketing Unapproved Products and Advance Legitimate Development
PR-M04-19-NI-031
Compounded Drugs
Statement from FDA on New 2019 Efforts to Improve the Quality of Compounded Drugs
PR-M04-19-NI-030
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