About Us
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BioProcess International provides the biotechnology industry with peer-reviewed editorial necessary to successfully drive products through the biopharmaceutical, biovaccine and biodiagnostic development process. BioProcess International covers the development and manufacture of biopharmaceutical applications including: proteins, peptides, hormones, vaccines, oligonucleotides, gene therapies, cell and tissue therapies, and biodiagnostics.
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Topics include:
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Our BPA audited circulation consists of 30,029 mid-to-upper managers working in all phases of the biotherapeutic development in the US, Europe and Canada.
Contact Information
BioProcess International
One Research Drive, Suite 400A
Westborough, MA 01581
UNITED STATES
Phone: 508-616-5550
Fax: 508-616-0476
Contact: Kim Rafferty
Hot Products
- Downstream Processing: May 2007 BioProcess International
- Single-Use Technologies: May 2007 Supplement
- Production: September 2007 BioProcess International
- BioProcess International Conference & Exhibition Official Pre-Show and On-Site Event Guide: September 2007 Supplement
- Quality/Bioanalysis: October 2007 BioProcess International
- BPI’s 5th Anniversary Issue: October 2007 Supplement: BPI’s 5th Anniversary Issue
- Downstream Processing: November 2007 BioProcess International
- Manufacturing/Compliance: December 2007 BioProcess International
Featured Articles
- Management Engagement Is Key To Successful Quality Systems
- Emerging Analytical Technologies For Biotherapeutics Development
- Current Status Of Protein Quantification Technologies
- CMOs Can Add Value To Outsourced Projects
- Delivery Technology Reenergizes DNA Drug Development
- Demonstrating Comparability For Well-Characterized Biotechnology Products
- Integrating Modular Design: Build Execution Strategies Into Biotech Projects
- How To Improve Your Implementation Of Two-Dimensional Preparative HPLC
- Comparing Shaker Flasks With A Single-Use Bioreactor For Growing Yeast Seed Cultures
- Cell Cultivation Process Transfer And Scale-Up
- Critical Issues In Outsourcing To A CMO
- Shared Risk: A Regulatory Management Strategy
- Cleaning And Cleaning Validation In Process Chromatography
- Regeneration Studies Of Anion-Exchange Chromatography Resins
- The Basics Of Cleaning And Cleaning Validation
- Special Challenges In Production Of Biopharmaceutical Dosage Forms
- Single-Use Bioreactors: A Brief Review Of Current Technology
- A Sensitive, Compact, In Situ Biomass Measurement System
- A Strategy For Developing A Monoclonal Antibody Purification Platform
- Comparing Automated And Manual Cell Counts For Cell Culture Applications
- Technical Transfer Of Manufacturing Processes From Client Sites To A CMO
- The Case for “Good Storage Practice” In Biopharmaceutical Development
- The Case for “Good Storage Practice” In Biopharmaceutical Development
- The Case for “Good Storage Practice” In Biopharmaceutical Development
- Critical Success Factors For Planning For Site Selection And Patient Recruitment Planning
- The Art And Science Of Auditing Clinical Trials
- Designing A Production Laboratory For Clinical Materials
- A Survey Of Bioassays In The Biopharmaceutical Industry
- The Case For XML Authoring And Content Life-Cycle Management
- Deactivation Of Single-Use Bioprocessing Systems Using Aqueous Chlorine Dioxide
- Smart Polymers Are In The Biotech Future
- Successful CMO Selection
- Successful CMO Selection: CMC Strategies For Outsourcing Biopharmaceutical Product Manufacturing
- Smart Polymers Are In The Biotech Future
- US Pharmacopeia Pharmaceutical Waters Part 3: General Information Chapters
- Analytical Technology And PAT
- Improved Expression Vector Activity Using Insulators And Scaffold/Matrix-Attachment Regions
- Mammalian Expression Cassette Engineering For High-Level Protein Production
- Mammalian Expression Cassette Engineering For High-Level Protein Production
- Mammalian Expression Cassette Engineering For High-Level Protein Production
- Mammalian Expression Cassette Engineering For High-Level Protein Production
- Application Of Disposable Pressure Sensors To A Postcentrifugation Filtration Process
- Quantifying Sterilizing Membrane Retention Performance
- Scaling Up From Bench Through Commercialization
- Process Development: Turning Science Into Technology
- Analytical Instrument Qualification
- Ultrasensitive Calorimetry: One Of The Best Kept (And Advanced) R&D Secrets?
- The Case For 'Good Storage Practice' In Biopharmaceutical Development
- A Bioassay Glossary
- Particle Counting Basics: Using Airborne-Particle Counters For ISO Certified Cleanrooms
- Design And Performance Of Viral Clearance Studies
- Mammalian Expression Cassette Engineering For High-Level Protein Production
- High-Throughput Screening Of Cell Lines Expressing Monoclonal Antibodies
- Bioreactor Control
- Bioreactor Monitoring, Modeling, And Simulation
- Building Process Control Into Chromatographic Purification Of Viruses, Part 2
- Building Process Control Into Chromatographic Purification Of Viruses, Part 1
- Cell Line Engineering Methods For Improving Productivity
- Special Challenges In Production Of Biopharmaceutical Dosage Forms
- A Practical Model For Outsourced Biomanufacturing
- Preparation Of Redundant, Disposable Filtration Systems
- A Simple Method For Evaluating Filtration Membranes
- Whole-Genome Evolution Technology: Improving Protein And Antibody Yields In Scalable Mammalian-Cell–Based Manufacturing
- Enterprise Resource Planning Systems
- Long-Term Stability Study And Topology Analysis Of Plasmid DNA By Capillary Gel Electrophoresis
- Rapid Isolation of Monoclonal Antibody Producing Cell Lines
- Post-Approval Research: Safety Net Or Power Tool?
- Successful Outsourcing Of Clinical Drug Developments
- Fourier-Transform Midinfrared Spectroscopy For Analysis And Screening Of Liquid Protein Formulations, Part 1
- Fourier-Transform Midinfrared Spectroscopy For Analysis And Screening Of Liquid Protein Formulations, Part 2
- Current And Future Frameworks For Cell- And Tissue-Based Products
- Biosimilars: A Portrait
- USP Pharmaceutical Waters, Part 1
- USP Pharmaceutical Waters, Part 2
- A Stirred-Tank Bioreactor: Delivered In Eight Weeks And One Hour
- Refolding Recombinant Human Granulocyte Colony Stimulating Granulocyte Colony Stimulating
- A Fully Disposable Monoclonal Antibody Manufacturing Train
- Incorporating Single-Use Systems In Biopharmaceutical Manufacturing
- Fed-Batch Mammalian Cell Culture In Bioproduction
- A 96-Well Plate Assay For Relative Monocolonal Antibody Titers
- Considerations For Aseptic Filling Of Parenterals
- The Market Need For Reconstitution Systems
- An Improved Method For Virus Filter Qualification And Implementation
- An Experimental Approach To Optimization Of Ultrafiltration
- A System Approach To Improving Yields In A Disposable Bioreactor
- Large-Scale Disposable Shaking Bioreactors: A Promising Choice
- Fourier-Transform Midinfrared Spectroscopy For Analysis And Screening Of Liquid Protein Formulations, Part 1
- Fourier-Transform Midinfrared Spectroscopy For Analysis And Screening Of Liquid Protein Formulations, Part 2
- Managing A Biopharmaceutical Supply Chain
- Key Considerations In Process Transfer
- Providing Sterility Assurance Between Stainless Steel And Single-Use Systems
- Evolving Toward Single-Use Bioprocessing: From Solutions To Holistic Value Creation
- Parenteral Packaging Concerns For Biotech Drugs: Compatibility Is Key
- If You Didn't Write It Down, It Didn't Happen
- Chlorine Dioxide, Part 2: A Versatile, High-Value Sterilant For The Biopharmaceutical Industry
- Addressing Product Improvement Using Chemical Modification In Biopharmaceutical Manufacture
- Sterility Assurance With Filtration: Taking Bioburden, Membrane Integrity, And Process Conditions Into Account
- Biopharmaceutical Filtration Validation: A Perspective On Regulations And Business Risk
- Large-Scale Disposable Shaking Bioreactors
- How Monosodium Glutamate Lot-To-Lot Variability Affects Process Performance Of Recombinant E.Coli
- Successful CMO Selection
- Technical Transfer Of Manufacturing Processes From Client Sites To A CMO
- Clinical Supplies Excellence: Are You Set Up To Succeed?
- Requirements For Outsourced Cold Chain Logistics And Storage In Biopharmaceutical Development
- Analytical Instrument Qualification
- Design And Scale-Up Of Bioreactors Using Computer Simulations
- Controlling And Monitoring Critical Stephen J. Davis
- Adaptive Automation Accelerates Process Development
- An Approach To Optimizing Large-Scale Cell Harvest
- Large-Scale Beta-Propiolactone Inactivation Of HIV For Vaccines
- Turning Science Into Technology
- From Aha! To Saving Lives
- Parenteral Packaging Concerns For Biotech Drugs
- The Critical Role Of Bioprocessing Contracts
- Using Liquid Nitrogen To Maximize Lyophilization Manufacturing Capacity
- The New GMP Environment For Investigational Medicinal Products In The European Union
- Outsourced Aseptic Fill/Finish And Stability Programs For Biopharmaceuticals
- What Are The Options? Many Questions, Many Choices
- NS0 Serum-Free Culture And Applications
- BVD Virus: Understanding And Managing The Hazard
- Bringing Together Software Audit Data For Regulatory Compliance
- CRO Industry Rides High On Emerging Opportunities In Eastern Europe
- Four Preparatory Steps To Successfully Refurbishing Pharmaceutical Production
- Biotech In Puerto Rico
- Strategies For Outsourcing Validation
- Environmental Monitoring
- Checking Pipette Performance On The Bench Top
- GMP Compliance And Pilot Plant Manufacture
- Case Study Of A Clinical-Scale CGMP Production Facility
- Case Study Of A Clinical-Scale CGMP Biopharmaceutical Production Facility
- Methods And Considerations For Disposable Implementation
- Strategies For Optimizing Today's Increasingly Disposable Processing Environments
- USP Pharmaceutical Waters, Part 1
- In-Line Buffer Dilution: The 'Killer App' For Process Analytical Technology
- Making An Informed Membrane Filter Choice
- Considerations For Use Of Disposable Technology In Contract Manufacturing
- Substantially Improved Stability Of Biological Agents In Dried Form
- Monitoring 'Live' Cell Concentrations In Real Time
- Designing A Concept Facility Based On Single-Use Systems
- Characterization Of Alternatives To Animal-Derived Raw Materials
- Characterization Of Microbial Seeds
- Aligning Expectations - Keys To Successful Contract Manufacturing
- Validation Of Pretrial ELIspot Measurements For Predicting Assay Performance During A Clinical Trial