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 August 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.
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Editorial
Preview
SPECIAL
REPORTS AND FEATURES
Focus: Obstacles to Manufacturing Innovation
PEER-REVIEWED
Establishing Acceptance Limits for Uniformity of Dosage Units: Part 2
DEVELOPMENT
-Biopharmaceutical APIs
-Drug Targeting
MANUFACTURING
Process Development: Using QbD in Process Development
QUALITY/REGULATIONS
Investigations/Root Causes
Avoiding Investigational Failure/Discrepancy-related Form 483 Observations
ANALYTICS
Lot Release Testing
Novel Metrics for Continuous Improvement Programs
OPERATIONS
Lab Operations
SUPPLY
CHAIN
Validating Supplier Quality
GLOBAL
REGULATION AND COMPLIANCE
-European Regulatory Watch
-Regulatory Watch
-Ask the Expert
BUSINESS/MARKET
FOCUS
-Outsourcing
Outlook
-Product Spotlight
-Pharma Capsules
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CLOSE IS JULY 28
Editorial Content
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