connecting the global pharma 2015 industry m e d i a...
TRANSCRIPT
Pharmaceutical Technology Europe provides objective and reliable editorial coverage of bio/pharmaceutical
manufacturing, process development, regulations, quality assurance and quality control, formulation, drug
delivery, API synthesis, analytical technology and testing, packaging and outsourcing. Our mission is to
report on current trends and key developments in the pharmaceutical industry and publish high quality
content, including peer-reviewed articles, case studies, roundtable discussions, and special features that will
help our readers in their daily decision-making and in implementing best practice.
CAPTURING PHARMA INNOVATION FOR MORE THAN 25 YEARS
BRANDING
AUDIENCE: CIRCULATION AND REACHPharmaceutical Technology Europe has a qualifi ed audience in Europe with 18,016* monthly subscribers; a fi gure that is qualifi ed biannually by BPA.
WHAT IS BPA?
BPA Worldwide is the global industry resource for verifi ed audience data. BPA delivers media audits of unsurpassed rigour, objectivity, accuracy, transparency and timeliness. BPA audits provide solid assurance for advertisers with rich, in-depth information about a magazine’s individual subscribers. All 18,016* subscribers meet strict qualifi cation criteria that ensure direct delivery of your advertising message to your target audience.
AUDITED ELECTRONIC MEDIA PRODUCTS
The BPA Brand Report includes a third-party validation of our online statistics, including our website and e-newsletters.
Please refer to your copy of the BPA audit to understand how our audience is represented in Europe by location, business function and market sector.
*June 2014 BPA Brand Report
AUdience
EDITORIAL FOCUSEach issue of Pharmaceutical Technology Europe addresses a key trend in drug development, including solid dosage and parenteral manufacturing, analytical testing, equipment and processing trends, quality by design, process analytical technology, API manufacturing, formulation and drug delivery. Through expert interviews, roundtable discussions, literature reviews and survey analysis, the editors report on emerging trends, strategies and best practices in these key areas.
PEER-REVIEWED RESEARCHPharmaceutical Technology Europe publishes peer-reviewed papers in the form of data-driven research papers, literature and patent reviews, application and technical notes and position papers on a broad range of drug development topics. All papers undergo a double-blind peer-review process by Pharmaceutical Technology Europe’s editorial advisory board, which consists of leading scientists, managers, directors and consultants.
KEY TOPICSFormulation/Drug Delivery: Solubility and bioavailability enhancement, nanotechnology, particle design and engineering, traditional and emerging dosage forms.
API Synthesis & Manufacturing: High potency, chiral chemistry, custom manufacturing, asymmetric synthesis, small- and large-molecule APIs.
Troubleshooting: Problems and solutions in equipment design and operation, and solid dosage, sterile and biopharmaceutical manufacturing.
Technical Q&A: Expert insight on analytical testing, data management, quality systems and more.
QA/QC: Quality metrics, product quality, process validation and statistical solutions.
Packaging Forum: Packaging equipment, containers, systems, and materials.
Facilities Design/Management: Key considerations for the design, operation and maintenance of GMP facilities.
Supply Chain/Logistics: Equipment, software and services to maintain a secure and compliant serialisation programme and supply chain.
Product Spotlight: New analytical instruments, automation and process control systems, information technology tools, laboratory equipment and manufacturing equipment.
REGULATION AND COMPLIANCERegulatory Watch: Legislation, court decisions, and regulatory changes in Europe and the United States.
Inside Standards: Industry associations and standard-setting bodies address compendial standards and guidances.
BUSINESS/MARKET FOCUSOutsourcing Outlook: Trends, partnerships and business activities in the contract services market, as described by Jim Miller of PharmSource Information Services and Eric Langer, president and managing partner of BioPlan Associates.
Global Market Reports: Reports from established and emerging pharmaceutical markets tackle both regulatory initiatives and market trends.
FocusProcess Validation
Special FeatureManufacturing Scale Up Strategies
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryControlled Release
API Synthesis & ManufacturingGlobal API Supply Chain
TroubleshootingEquipment Design and Operation
Technical Q&AAnalytical Testing for Biologics
Packaging ForumPharmapack Review
Columns Regulatory WatchEMA UpdateOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsINTERPHEX, 21-23 April, New York
Value-Addede-News Product/Service Profile
FocusAPI Development and Manufacturing
Special FeatureTransdermal Drug Delivery
Regulars
Peer-Reviewed Technical NotesAPI Synthesis & ManufacturingPolymorphism and Crystallisation and DCAT Roundup
TroubleshootingSolid Dosage
Technical Q&AData Management in Manufacturing
QA/QCBiologics Raw Materials
Supply Chain/LogisticsSerialisation
Columns Regulatory WatchInside StandardsOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsAchema, 15-19 June, Frankfurt, Germany
Value-Added1/2-Page Achema Exhibiitor Profile
FocusProcess Analytical Technology
Special FeatureBiopharmaceutical Manufacturing
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryOrally Inhaled and Nasal Drug Products
API Synthesis & ManufacturingHazardous Reagent Chemistry
TroubleshootingAseptic Processing/Sterile Manufacturing
QA/QCStatistical Solutions
Facilities Design/OperationsClean Zone Definitions
Columns Regulatory WatchEMA UpdateOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsBIO International Convention, 15-18 June, Philadelphia
Value-Added1/3 Page Product/Service Profile
PHARMACEUTICAL TECHNOLOGY EUROPE 2015 EDITORIAL CALENDAR
FocusExcipients
Special FeatureSolid Dosage Packaging
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryBiologics
API Synthesis & ManufacturingCustom Manufacturing Outlook
TroubleshootingAseptic Processing/Sterile Manufacturing
Technical Q&AExtractables and Leachables
QA/QCStatistical Solutions
Columns Regulatory WatchInside StandardsOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsInformex USA, 3-5 Feb., New OrleansGlobal Drug Delivery and Formulation Summit, 9-11 Feb., Dusseldorf, GermanyPharmapack, 11-12 Feb., Paris
Value-AddedReadex Advertising Study1/2-Page Pharmapack Exhibiitor Profile
FocusCold Chain
Special FeatureAnalytical Testing and Instruments
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryParticle Engineering/Nanotechnology
API Synthesis & ManufacturingChiral Chemistry
TroubleshootingSolid Dosage
Technical Q&AVisual Inspection Techniques
QA/QCProduct Quality: Biologics
Columns Regulatory WatchEMA UpdateOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsBiological Production Forum, 2-4 March, Dusseldorf, GermanyPittcon, 8-12 March, New OrleansBIO-Europe Spring, 9-11 March, Paris
Value-Addede-News Product/Service Profile
FocusElemental Impurities
Special FeatureLyophilisation
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliverySemi-solid Dosage Forms
API Synthesis & ManufacturingHigh-Potency Manufacturing
TroubleshootingBiopharmaceutical Manufacturing
QA/QCInvestigations/Root Causes
Facilities Design/OperationsGMP Considerations in Room Design
Columns Regulatory WatchInside StandardsOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
Special Themed Issue
Outsourcing IssueThis supplement reviews the European market for outsourcing pharmaceutical manufacturing and drug development. Articles will focus on best practices for choosing suppliers, including strategies for ensuring quality control in the supplier relationship, vendor selection, negotiating contracts, performing due diligence, technology transfer, and intellectual property protection.
ShowsPDA Annual Meeting, 16-18 March, Las Vegas, NV USABDP Week, 30 March-2 April, Huntingdon Beach, CA USA
Value-Added1/3 Page Product/Service Profile
Ad Close: 15 December* Ad Close: 16 January* Ad Close: 17 February* Ad Close: 16 March* Ad Close: 16 April* Ad Close: 15 May*
january february march april may june
eDiTOrial SubmiSSiOnS anD DeaDlineS**Pharmaceutical Technology Europe welcomes article pitches and abstracts for regulatory, technical, and peer-reviewed articles throughout the year. Submit your inquiry four months prior to publiation date. Contact Rita Peters, editorial director, ([email protected]) to submit or for futher information.
FocusQuality by Design for Solid Dosage Manufacturing
Special FeatureRoom declassification in biopharma facility
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryTaste-masking
API Synthesis & ManufacturingLow Temperature Chemistry
TroubleshootingAseptic Processing/Sterile Manufacturing
Technical Q&AModular/Flexible Manufacturing
QA/QCQuality Metrics
Columns Regulatory WatchInside StandardsOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsCPhI Worldwide, 13th -15th October, MadridBiotechnica, 6-8 October,Hanover, Germany
Value-Added1/2-Page CPhI Exhibiitor Profile
FocusBioavailability/Solubilisation
Special FeatureEquipment Cleaning
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryGI Targeting
API Synthesis & Manufacturing“Process Intensification/Continuous Flow Manufacturing”
TroubleshootingBiopharmaceutical Manufacturing
QA/QCOperational Excellence
Packaging ForumSolid Dosage Packaging
Columns Regulatory WatchInside StandardsOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsControlled Release Society, 26-29 July, Edinburgh, Scotland
Value-Addede-News Product/Service Profile
FocusRisk Assessment and Mitigation
Special FeatureEquipment and Manufacturing Trends
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryHigh Potency Drug Formulation
API Synthesis & ManufacturingBiopharmaceutical Manufacturing
TroubleshootingEquipment Design and Operation
Technical Q&ALean Manufacturing
Supply Chain/LogisticsShipping Services
Columns Regulatory WatchEMA UpdateOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
Special Themed Issue
Pharma Development Expertise: Regional FocusThis supplement showcases the expertise of companies serving the pharmaceutical industry across Europe, with special focus on Germany, France, Italy and Benelux. Coverage includes technologies for solid dosage manufacturing, sterile fill and finish, bioprocessing and analyticaltesting.
Value-AddedReadex Advertising Study1/3-Page Product/Service Profile
Ad Close: 16 June* Ad Close: 16 July* Ad Close: 14 August* Ad Close: 16 September* Ad Close: 16 October* Ad Close: 16 November*
july auguST SepTember OcTOber nOvember December
FocusContinuous Solid Dosage Manufacturing
Special FeatureLarge Volume vs. Small Volume Parenteral Manufacturing
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliverySpecialty Dosage Forms
API Synthesis & ManufacturingHeterocyclic Chemistry in API Manufacturing
TroubleshootingEquipment Design and Operation
QA/QCImplementing Corrective and Preventive Action (CAPA)
Supply Chain/LogisticsTrack and Trace
Columns Regulatory WatchInside StandardsOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
Value-Added1/3-Page Product/Service Profile
FocusAPI Review and Outlook
Special FeatureEmerging TherapeuticsSalary and Employment Survey
Regulars
Peer-Reviewed Technical NotesFormulation/Drug DeliveryCombination Products
TroubleshootingBiopharmaceutical Manufacturing
Technical Q&ABiosimilars
QA/QCProduct Quality: Solid/Semi-solid Dosage
Facilities Design/OperationsRoom Pressurization
Columns Regulatory WatchEMA UpdateOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
Value-AddedFull-Page Corporate Profile
FocusAntibody Drug Conjugates
Special FeatureDrug Reformulation Strategies
Regulars
Peer-Reviewed Technical NotesAPI Synthesis & ManufacturingFluorination Chemistry in API Manufacturing
ßTroubleshootingSolid Dosage
Technical Q&AProcess Controls
QA/QCCritical Quality Attributes
Packaging ForumParenterals Packaging
Columns Regulatory WatchEMA UpdateOutsourcing ReviewMarket ReportBio/Pharma Q&AProduct SpotlightAsk the Expert
ShowsAAPS, 25-29 Oct, Orlando
Value-Addede-News Product/Service Profile
PHARMACEUTICAL TECHNOLOGY EUROPE 2015 EDITORIAL CALENDAR
Editorial content may change at the discretion of the editor.*Advertising deadlines may be subject to change.** Receipt of an article or abstract does not guarantee inclusion in a particular issue of the magazine or on
www.PharmTech.com
DIGITAL MEDIA OPPORTUNITIES
PharmTech.com
Key advertising benefi ts: global platform, brand exposure, measurable ROI
With 43,535* globally located monthly unique users, www.pharmtech.com is the leading online resource for the global pharmaceutical industry. We provide a number of advertising solutions across the website including banner adverts, white papers and an on demand webinar section.
PHARMACEUTICAL TECHNOLOGY NEWSLETTERS
Key advertising benefi ts: brand exposure, targeted audience, direct delivery
Pharmaceutical Technology produces a series of newsletters aimed at different job functions and geographical locations within the pharmaceutical industry. All our newsletters are requested by our audience, increasing open rates and advertisement response:
• Pharmaceutical Technology Europe weekly newsletter (European audience, 11,299 recipients)
• Pharmaceutical Technology weekly newsletter, ePT (global audience of 20,995 recipients)
• PT Sourcing & Management Newsletter (16,184 global manufacturing & supply chain recipients)
• Equipment & Processing Report showcasing processing equipment & manufacturing processes (19,891 recipients)
• Whitepaper alert promoting a selection of third party white papers to a high quality audience – an excellent lead generation opportunity
WEBCASTS
Pharmaceutical Technology’s popular & successful webinar program is the perfect content marketing and lead generation solution for clients wishing to engage our audience, and demonstrate their expertise on a wide spectrum of topics.
CAST
CAST is our Custom Audience Segmentation Tool offering unparalleled access to a database of almost 1 million contacts. With CAST we can direct your marketing message to a targeted global audience of pharmaceutical industry decision makers using a number of advanced fi lters, ensuring your investment only reaches a relevant audience and maximising the opportunity for client conversion.
We have a number of digital solutions not listed in this media planner. Please see our individual digital media planner or contact your sales representative for more information.
*June 2014 BPA Brand Report
1x 3x 6x 9x 12x 24x
Full Page 7,500 6,955 6,580 6,430 6,130 5,980
2/3 Page 6,730 6,060 5,720 5,385 5,050 4,700
1/2 Page 5,230 4,710 4,450 4,200 3,925 3,665
1/3 Page 4,100 3,700 3,495 3,300 3,080 2,880
1/4 Page 3,370 3,030 2,865 2,695 2,530 2,360
6 months 12 months
Super Maxi Box 5,040 6,720
Maxi Box 4,115 5,430
Maxi Box 2,965 3,950
Homepage per month
Interstitial Pop-up Banner (640 x 480) 3,929
Peel Down 3,000
Leadboard (728 x 90) 1,857
Box (300 x 250) 1,857
Rectangle (300 x 100) 1,071
Sponsored Text 464
Featured Whitepaper 1,071
Contact your sales representative for pricing
1x 4x
Leaderboard (728 x 90) 1,130 3,990
Skyscraper (160 x 600) 920 3,255
Headline Banner (468 x 60) 840 2,940
Banner (468 x 60) 735 2,570
Product / Event Profi le 655 2,310
Full Page 5,245
1/2 Page 3,410
1/4 Page 2,360
Up to 20g
< 5000 (Rate per ‘000) 800
> 5000 (Rate per ‘000) 690
Full Circulation (Rate per ‘000) 450
Outside Back Cover 1,000
Inside Front Cover 900
Inside Back Cover 700
Preferred Position 600
Double Page Spread 12,000
Bellyband** 9,500
Tip-on** 9,000
€ EURO PRICING 2015PRINT
€ EURO PRICING & AD SPECS 2015DIGITAL & WEB
DISPLAY POSITIONS (4 COLOUR) (€)
PREMIUM DISPLAY POSITIONS* (€) SPECIAL DISPLAY POSITIONS* (€)
CLASSIFIED POSITIONS* (€)
WEBSITE (€) WHITEPAPER MONTHLY NEWSLETTER (€)
WEBCASTS & SURVEYS
PTE WEEKLY NEWSLETTER (€)
RECRUITMENT POSITIONS (€) MAGAZINE INSERTS (€)
Rates and sizes correct at time of going to press.*Premium and Special Position charges are in addition to the published print rates for Colour Display Advertising.** Includes production and printing
PTE GROUP AD SIZES For all print products. Keep live matter 10 mm from all sides
NON-BLEED BLEED TRIM SIZE NON-BLEED BLEED TRIM SIZE
Two page spread 368 x 241 400 x 273 394 x 267 1/2 page horizontal 171 x 117 203 x 137 197 x 133
Full Page 171 x 241 203 x 273 197 x 267 1/3 page vertical 54 x 241 73 x 273 70 x 267
2/3 Page 114 x 241 133 x 273 130 x 267 1/3 square 114 x 117 133 x 137 130 x 133
1/2 Island 114 x 178 133 x 197 130 x 194 1/4 page 86 x 117 105 x 137 102 x 133
1/2 page vertical 86 x 241 105 x 273 102 x 267
CONTACTS
Full page 2/3 page 1/2 page island 1/2 page vertical
1/2 page horizontal 1/3 page vertical 1/3 square 1/4 page
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