Resource for professionals in the BioResearch industry- Information on BioPharm Contract Manufacturing, BioPharm Processing, BioResearch Technology, BioPharm Manufacturing, Mixing
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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.

Topics include:
  • Fermentation and Cell Culture
  • Separation & Purification
  • Manufacturing
  • Bioanalytical Methods & Assay Development
  • Validation & Quality Issues
  • Regulatory Compliance
  • Formulation
  • Single-Use Technologies
  • Economic Development
  • Contract Services and Outsourcing
  • Fill & Finish
  • Drug Delivery
  • Information Technology

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.



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Contact Information     
BioProcess International
One Research Drive, Suite 400A
Westborough, Massachusetts 01581
UNITED STATES
Phone: 508-616-5550
Fax: 508-616-0476
Contact: Kim Rafferty

Hot Products     
BioProcessIntllogo
Downstream Processing: May 2007 BioProcess International
Single-Use Technologies: May 2007 Supplement
Manufacturing/Compliance: June 2007 BioProcess International
The Industry Yearbook: July/August 2007
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
Quality/Bioanalysis: October 2007 BioProcess International
Downstream Processing: November 2007 BioProcess International
Manufacturing/Compliance: December 2007 BioProcess International

Featured Articles     
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


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