Pharmaceutical Technology Europe
June 2017 Advertising Opportunity
Since 1989, 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. All subscribers meet strict qualification criteria that ensure direct delivery of your advertising message to your target audience.

Pharmaceutical Technology Europe has a qualified audience in Europe with over 18,300 monthly subscribers.(Alliance for Audited Media June 2016 Initial Audit Report).

Here is the June editorial lineup to give you a heads up on the coverage in this issue and to assist you in your decision to advertise in Pharmaceutical Technology Europe.
VALUE ADDED
Marketing package with your June display ad:
e-News Product/Service Profile
(Ask your rep for details.)
SHOW DISTRIBUTION
This issue will be at the following industry event:
BIO International Convention, 19 - 22 June, San Diego
ADVERTISING OPPORTUNITIES
Pharmaceutical Technology offers multi-platform suite of print, digital, and content marketing solutions www.PharmTech.com/contentmarketing
  • Website
    • www.PharmTech.com
  • Print Publication & Supplements
  • Content Marketing Solutions
    • Dedicated Dialogue
    • Solution Center
    • Mobile Apps
    • Podcasts
  • Pharma Marketplace
  • Digital Edition
  • E-Books
  • Custom Audience Segmentation Tool (CAST)
    • Content Targeting to the Right Audience
  • Webinars
  • E-Newsletters
*Ask about our Lead Nurturing Program and Native Advertising.
Editorial Preview
SPECIAL REPORTS AND FEATURES
Overcoming Biomanufacturing Challenges
Boosting Bioproduction Workflows with Automation Technologies
PEER-REVIEWED
Technical Application Note: A Forensic Microscopy Approach to Identification of Particulate Matter Observed in a Sterile Ophthalmic Solution on Stability
DEVELOPMENT
-Catalysis
Biocatalysts for Cannabinoid Synthesis
-Solubility
Micronization
MANUFACTURING
-Inhalation Drug Manufacturing
The Relevance of E&L Testing for MDIs, DPIs, and Other Drug Products Applied by Inhalation
-Equipment and Operation
QUALITY/REGULATIONS
Process Validation
Stage 2 Process Validation: Regulatory Expectations and Approaches to Determine and Justify the Number of PPQ Batches
ANALYTICS
Dissolution Testing
OPERATIONS
Facility Design and Operations
SUPPLY CHAIN
Supply Chain: Anticounterfeiting
Why Serialization Isn’t Enough
GLOBAL REGULATION AND COMPLIANCE

-European Regulatory Watch

-US Regulatory Watch
-Ask the Expert

BUSINESS/MARKET FOCUS
-Outsourcing Outlook
-Product Spotlight
-Pharma Capsules
AD CLOSE IS MAY 25
Editorial Content Subject to Change
Pharma Marketplace
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Contact
Stephen Cleland
Senior Sales Executive
Tel: +44 (0) 151 353 3647
stephen.cleland@ubm.com
Linda Hewitt
Sales Manager
Tel: 44 (0) 151 353 3520
linda.hewitt@ubm.com