Saturday December 28, 2024
|
Subscribe
|
Contribute
|
About
|
Access Your Account
|
Register
|
Login
|
Home
|
Issue Archive
|
Featured Reports
|
eBooks
|
BioProcess Insider
|
Multimedia
|
BPI White Papers
|
Webinars
|
Posters
|
BioProcess International Events
|
BioProcess International US West
|
BioProcess International Europe
|
BioProcess International Academy
|
Events
Covering the whole development process for the global biotechnology industry
Upstream
Processing
Bioprocessing begins upstream, most often with culturing of animal or microbial cells in a range of vessel types (such as bags or stirred tanks) using different controlled feeding, aerating, and process strategies.
Assays
Biochemicals/Raw Materials
Bioreactors
Cell Culture Media
Expression Platforms
Fermentation
Perfusion Cell Culture
Upstream Contract Services
Upstream Single-Use Technologies
Downstream
Processing
Beginning with harvest of material from a bioreactor, downstream processing removes or reduces contaminants to acceptable levels through several steps that typically include centrifugation, filtration, and/or chromatographic technologies.
Filtration
Separation/Purification
Viral Clearance
Chromatography
Downstream Contract Services
Downstream Single-Use Technologies
Manufacturing
Drug products combine active pharmaceutical ingredients with excipients in a final formulation for delivery to patients in liquid or lyophilized (freeze-dried) packaged forms — with the latter requiring reconstitution in the clinical setting.
Personalized Medicine
Single Use
Supply Chain
Vaccines
MAb
Biosimilars
Cell/Gene Therapies
Emerging Therapeutics
Facility Design/Engineering
Continuous Bioprocessing
Fill/Finish
Formulation
Information Technology
Manufacturing Contract Services
Process Monitoring and Controls
Analytical
Many technologies are used to characterize biological products, manufacturing processes, and raw materials. The number of options and applications is growing every day — with quality by design (QbD) giving impetus to this expansion.
Culture Development
Cell Line Development
Downstream Development
Downstream Validation
Laboratory Equipment
PAT
Pre-Formulation
Product Characterization
QA/QC
Upstream Development
Upstream Validation
Leachables/Extractables/Particulates
Business
Even as it matures, the biopharmaceutical industry is still a highly entrepreneurial one. Partnerships of many kinds — from outsourcing to licensing agreements to consultancies — help companies navigate this increasingly global business environment.
Careers
CMC Forums
Economics
Intellectual Property
Pre-Clinical and Clinical Trials
Regulatory Affairs
Risk Management
BioRegions
Author Archives:
BPI Contributor
Considerations for Aseptic Filling of Parenterals
by
BPI Contributor
Design and Performance of Viral Clearance Studies
by
BPI Contributor
Products, Services, and Literature
by
BPI Contributor
The Expanding Role of Biologics in the Pharmaceutical Industry
by
BPI Contributor
The Market Need for Reconstitution Systems
by
BPI Contributor
Vaccines: Quality Control, Scale-Up, and Manufacture
by
BPI Contributor
Cell Culture and Upstream Processing
by
BPI Contributor
Comparing Automated and Manual Cell Counts for Cell Culture Applications
by
BPI Contributor
Conference-at-a-Glance
by
BPI Contributor
Criteria for Selection of IgG Isotype and Glycoform of Antibody Therapeutics
by
BPI Contributor
Page 156 of 233
<
1
...
151
152
153
154
155
156
157
158
159
160
...
233
>
Home
Issue Archive
â–¼
Featured Reports
eBooks
BioProcess Insider
Multimedia
â–¼
BPI White Papers
Webinars
Posters
BioProcess International Events
â–¼
BioProcess International US West
BioProcess International Europe
BioProcess International Academy
Events
