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CELEBRATING 30 YEARS WITHmoRE THAN 31,000 SUBSCRIBERS
www.BioPharmInternational.com
Covering the biopharmaceutical developmentand manufacturing industry since 1988
2018 EDITORIAL CALENDAR
www.BioPharmInternational.com
CELEBRATING 30 YEARS WITH moRE THAN 31,000 SUBSCRIBERS
Editorial CovEragE
EXPERT INSIGHT AND ANALYSIS
BioPharm International provides the biopharmaceutical industry with comprehensive coverage of key scientific, technology, regulatory, and business topics. The editorial mix of peer-reviewed papers, practical advice on managing bioprocessing and technology, regulatory and business columns, and expert commentary provides comprehensive coverage of upstream and downstream processing, manufacturing operations, regulations, formulation, scale up/technology transfer, drug delivery, analytical testing, and more.
The insight and analysis covers biologic-based therapies including monoclonal antibodies, biosimilars/biobetters, protein therapeutics, vaccines, cell/gene therapies, antibody drug conjugates, and other emerging therapies.
Special iSSueSJuly BioPharm International’s 30th Anniversary IssueDuring the past 30 years, BioPharm International has chronicled advances in biologic drug development and manufacturing, providing insight and analysis of key science and business trends. In this commemorative 30th anniversary issue, the editors track these developments and make projections for the future.
MarchOutsourcing Resources eBookHow are contract development and manufacturing contract service organizations meeting the development and manufacturing needs of innovator biopharmaceuticals and biosimilars companies? The editors examine trends, partnerships, manufacturing capacity, regulatory, supply chain, and technical expertise issues.
June Single-Use Systems Advance Commercial Production eBookAs more therapies developed using single-use technologies are approved, the industry must address any hurdles that may hinder the widespread adoption of single-use systems for commercial production. The editors examine the technology, practices, and regulatory approval questions that remain.
October Best Practices for Today’s Biopharma Laboratory eBookAnalytical studies are vital to every step of biologic drug research, development, and quality control. The editors report on the latest trends in analytical techniques, as well as new instruments, equipment, and supplies used in the analysis of raw materials, drug substances, and drug products.
Through expert interviews, roundtable discussions, literature reviews, and survey analyses, the editors report on emerging trends, strategies, and best practices in these key areas.
To learn about contributions, visit www.biopharminternational.com/biopharm-international-info-authors.
EDITORIAL FEATURES
Peer-Reviewed Research Papers
BioPharm International publishes peer-reviewed papers in the form of technical case studies/application notes; topical literature or patent reviews; novel research; or science-based opinion papers. All papers undergo a double-blind peer-review process by BioPharm International’s Editorial Advisory Board of leading scientists, managers, directors, and consultants.
Technical Articles
Feature articles in BioPharm International offer timely technical and scientific discussions of ongoing drug development challenges and solutions. Articles are authored by industry experts and the magazine’s editorial team. Topics cover the full spectrum of biopharmaceutical development and manufacturing including upstream processing, downstream processing, manufacturing, quality and regulations, analytics, facilities and equipment, laboratory operations, packaging, logistics, supply chain, and business issues including intellectual property, market research, and funding.
Regulatory Beat
The latest developments, guidance documents, and enforcement action from international regulatory authorities, as well as expert analysis, are addressed in this monthly feature.
Perspectives on Outsourcing
Contract service providers and users stay current on trends, partnerships, and business activities through the Perspectives on Outsourcing column.
Product Spotlight
New products for bioprocessing applications and analytical testing are profiled in each issue.
Ask the Compliance Expert
Questions about enforcement, standard operating procedures, working with FDA, and other compliance issues are answered by regulatory experts.
www.BioPharmInternational.com
CELEBRATING 30 YEARS WITH moRE THAN 31,000 SUBSCRIBERS
2018 ediTorial calendarJanuaryAd Close: December 7, 2017
focus » 2018 Biopharma Outlook
peer-reviewed research/technical notes
early Development pipeline » Monoclonal Antibodies
Upstream processing » Cell Culture
Downstream processing » Separation and Purification
manufacturing » Fluid Handling Systems
Quality/regulations » API Development and
Approval Trends
analytics » Stability Testing
operations » Process Monitoring/Controls
supply chain » Track and Trace/Serialization
outsourcing » Perspectives on Outsourcing
BioBusiness » Economic Development
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » Product/Service Profile in BioPharm
International’s e-Bulletin Newsletter
shows » CASSS – WCBP, Jan. 30–Feb. 1,
Washington, DC
FebruaryAd Close: January 9
focus » Analytical Instruments and Methods
peer-reviewed research/technical notes
Upstream processing » Biologic-Drug Formulation
Downstream processing » Single-Use Manufacturing
manufacturing » Cell/Gene Therapies Development
Quality/regulations » Critical Quality Attributes
analytics » Lab Data Integrity
operations » Facilities
packaging » Container Closures
outsourcing » Outsourcing Analytics
BioBusiness » Global Biopharma Markets
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » Pittcon Preview in BioPharm
International’s e-Bulletin Newsletter
shows » Pittcon, Feb. 26–March 1, Orlando
MarchAd Close: February 7focus » Biologic-Drug Development Trends
peer-reviewed research/technical notes
early Development pipeline » Antibody-Drug Conjugates
Upstream processing » Process Modeling
Downstream processing » Process Controls
manufacturing » Fill/Finish
Quality/regulations » Quality Agreements
analytics » Analytical Best Practices
operations » Lab Operations
supply chain » Cold Chain
outsourcing » Perspectives on Outsourcing
BioBusiness » Intellectual Property
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » INTERPHEX Exhibitor Guide in
BioPharm International’se-Bulletin Newsletter
» Interphex Exhibitor Guide (Print)shows » BioProcess International West,
March 19–22, San Francisco, CA » PDA Annual Meeting, March
19–21, Orlando, FL » World Vaccines Congress,
April 3–5, Washington, DCspecial themed e-BookOutsourcing ResourcesAn annual review of the market for outsourced contract services, regulatory topics, manufacturing, development, and supply chain issues.
www.BioPharmInternational.com
CELEBRATING 30 YEARS WITH moRE THAN 31,000 SUBSCRIBERS
2018 ediTorial calendarAprilAd Close: March 12
focus » Biologics-Drug Delivery Systems
peer-reviewed research/technical notes
Upstream processing » Single-Use Systems
Downstream processing » Process Chromatography Selection
manufacturing » Biosimilars/Biobetters Development
Quality/regulations » Equipment Qualification
analytics » Protein Characterization
operations » Equipment
packaging » Aseptic Manufacturing Processes
outsourcing » Outsourcing Development
BioBusiness » Investment Outlook
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » CPhI North America Exhibitor
Guide in BioPharm International’s e-Bulletin Newsletter
» CPhI North America Exhibitor Guide (Print)
shows » INTERPHEX, April 17–19, New York » CPhI North America, April
24–26, Philadelphia
MayAd Close: April 11
focus » Continuous Biomanufacturing
peer-reviewed research/technical notes
early Development pipeline » Cell/Gene Therapies
Upstream processing » Cell Line Quality
Downstream processing » Viral Clearance
manufacturing » Single-Use vs. Stainless Steel
Quality/regulations » International Regulations
analytics » Cleaning Validation
operations » Process Monitoring/Controls
supply chain » Logistics/Shipping
outsourcing » Perspectives on Outsourcing
BioBusiness » Market Research Update
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » BIO International Enhanced
Exhibitor Showcase (1/4 page equivalent)
» BIO Preview in BioPharm International’s e-Bulletin Newsletter
shows » BIO International Convention,
June 4–7, Boston
June Ad Close: May 10
focus » Fill/Finish Quality
peer-reviewed research/technical notes
Upstream processing » Bioreactors
Downstream processing » Cell Harvesting
manufacturing » Protein Therapeutics Development
Quality/regulations » Process Validation
analytics » Adventitious Agent Testing
operations » Facilities
packaging » Clinical Trial Materials
outsourcing » Outsourcing Manufacturing
BioBusiness » Partnering
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print)
special themed e-BookSingle-Use Systems Advance Commercial ProductionA review of new technologies and processes that are helping to drive the adoption of single-use systems for the commercial production of biologic-based drugs.
www.BioPharmInternational.com
CELEBRATING 30 YEARS WITH moRE THAN 31,000 SUBSCRIBERS
2018 ediTorial calendarJulyAd Close: June 12
focus » BioPharm International’s
30th Anniversary Issue
peer-reviewed research/technical notes
early Development pipeline » Biosimilars/Biobetters
Upstream processing » Advances in Upstream Processing
Downstream processing » Advances in Downstream Processing
manufacturing » Advances in Manufacturing
Quality/regulations » Quality Advances
analytics » Advances in Analytics
operations » Equipment
packaging » Advances in Packaging
outsourcing » Perspectives on Outsourcing
BioBusiness » Economic Development
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » FREE Product/Service
Innovation Profile Page (Full-page Advertisers)
AugustAd Close: July 11
focus » Cell Line Development
peer-reviewed research/technical notes
Upstream processing » Expression Systems
Downstream processing » Residual Impurities
manufacturing » Cell/Gene Therapies Development
Quality/regulations » Investigations/Root Causes
analytics » Extractables and Leachables Testing
operations » Lab Operations
supply chain » Cold Chain
outsourcing » Outsourcing Analytics
BioBusiness » Managing Risk
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » FREE Ad Performance Study
SeptemberAd Close: August 10focus » Increasing Bioprocessing Efficiencies
peer-reviewed research/technical notes
early Development pipeline » Protein Therapeutics
Upstream processing » Raw Materials
Downstream processing » Batch vs. Continuous Processing
manufacturing » Process Analytical Testing
Quality/regulations » Quality by Design
analytics » Microbial Contamination
operations » Facilities
packaging » Vials
outsourcing » Perspectives on Outsourcing
BioBusiness » Intellectual Property
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » Product/Service Profile in BioPharm
International’s e-Bulletin Newslettershows » PDA/FDA Joint Regulatory Conference,
Sept. 9–12, Washington, DC » CPhI Worldwide, Oct. 9–11,
Madrid, Spain
www.BioPharmInternational.com
CELEBRATING 30 YEARS WITH moRE THAN 31,000 SUBSCRIBERS
2018 ediTorial calendarOctoberAd Close: September 11
focus » Single-Use Systems
peer-reviewed research/technical notes
Upstream processing » Glycosylation
Downstream processing » Lyophilization
manufacturing » Monoclonal Antibodies Development
Quality/regulations » Mock Inspections
analytics » Analytical Best Practices
operations » Process Monitoring/Controls
supply chain » Raw Materials Tracking
outsourcing » Outsoucing Development
BioBusiness » Investment Outlook
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » Free 3-minute Podcast - posted
online and e-mailed (one month) » AAPS Preview in BioPharm
International’s e-Bulletin Newsletter
shows » AAPS 2018 PharmSci360,
Nov. 4–7, Washington DCspecial themed e-BookBest Practices for Today’s Biopharma LaboratoryMethod development, analytical techniques, and profiles of new instruments, equipment, and supplies used in the testing and analysis of raw materials, drug substances, and drug products.
NovemberAd Close: October 11
focus » Scale-Up vs. Scale-Down
peer-reviewed research/technical notes
early Development pipeline » Cell/Gene Therapies
Upstream processing » Media and Supplements
Downstream processing » Manufacturing Data Integrity
manufacturing » Manufacturing Best Practices
Quality/regulations » Risk Assessment and Mitigation
analytics » Biosimilar Analysis
operations » Equipment
packaging » Prefilled Syringes
outsourcing » Perspectives on Outsourcing
BioBusiness » Market Research Update
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » Free Listing in BioPharm’s
Knowledge Resources Newsletter (Lead Generation)
DecemberAd Close: November 8
focus » The Quality Issue » Special Report: Annual
Employment Survey
peer-reviewed research/technical notes
Upstream processing » Bioreactor Performance
Downstream processing » Bioburden Reduction
manufacturing » Antibody Drug Conjugates
Development
Quality/regulations » Lot Release Testing
analytics » Endotoxin Testing
operations » Lab Operations
supply chain » Validating Supplier Quality
outsourcing » Outsourcing Manufacturing
BioBusiness » Partnering
Departments » Regulatory Beat » Product Spotlight » Ask the Compliance Expert
value-added » New Tech Showcase (Print) » Corporate Profile in the Corporate
Capabilities Section (Ask your sales representative for details.)