Breaking News on Contract Research, Manufacturing & Clinical Trials

Supply chain, logistics


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High Potency Manufacturing - Key selection criteria when evaluating an outsourcing partner - Alkermes

08-Apr-2014 - Many companies are choosing to outsource the manufacture of their highly potent compounds.  A provider of contract pharma services in high potent manufacturing, Alkermes Contract Pharma Services, outlines elements that should be considered  when outsourcing secondary processing (i.e. dosage form...
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A year on, EU GDP’s affect on European Pharma Distribution - World Courier

24-Mar-2014 - World Courier welcomed the EU GDP guidelines, which created a yardstick by which logistics providers could be measured and compared.  A year on from the draft publication it is now fully in force and there has already been an update...
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Forecasting strategies to optimize clinical trials - Almac Group

03-Mar-2014 - In a market that is constantly evolving, where rising complexities and costs associated with product development and clinical trial conduct present new clinical supply chain challenges, conventional forecasting methods may not provide an adequate solution.  Add to this the increasing...
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Ensuring cold chain remains cold and controlled room temp remains controlled! - World Courier

24-Feb-2014 - The first of ten new vehicles have been delivered to World Courier Ground Europe, and in line with the requirements of the regulations for pharmaceutical distribution have undergone qualification testing for frozen, refrigerated and controlled room temperature conditions at extreme...
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Customs Declared Value - What this means for the global clinical supply chain - Marken

22-Nov-2013 - What valuation is and how is it used by Customs authorities and other government agencies How to use the six approved valuation methods to correctly determine the customs value of your study shipments Why using the correct declared value is important for...
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Controlled Release and Bioavailability Enhancement -

28-Oct-2013 - Metrics provides product development that leverages proprietary pharmaceutical technologies in the areas of: •    Customized Controlled Release Drug Delivery •    Bioavailability Enhancement •    Taste Masking (liquid and solid presentations)When applied appropriately, these technologies can deliver therapeutic and convenience benefits to...
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Optimizing your Strategy and Budget for Clinical Trial Supply Distribution - Marken

25-Oct-2013 - This presentation will discuss: How to determine if a depot or direct to site shipments are more efficient Calculation based on a case study How to avoid delays and assure that your shipments arrives without delays and excursions
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New Guidelines for Stabilization of Proteins by Freeze Drying: Formulation and Process Heresy - Baxter

17-Oct-2013 - Over the years a number of informal guidelines or “rules” for the formulation and processing of proteins for freeze-drying have been developed. However, in recent years it has become obvious that some of these rules need modification. In this presentation,...
Watch now!On-Demand Supplier Webinar

Trade Compliance and Pharma: What you need to know about the trade aspects of your global studies - Marken

25-Sep-2013 - This webinar will explore the basics of trade compliance for pharmaceutical products: Overview of global trade compliance Trade compliance and pharmaceutical products Understanding the import clearance process Consider the role that different government agencies play in trade compliance Tips for managing compliance with trade regulations ...
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Exploring New Frontiers in Direct to Patient Home Delivery Services for Clinical Trials Materials - Marken

07-Aug-2013 - Exploring New Frontiers in Direct to Patient (DTP) Home Delivery Services for Clinical Trial Materials provides an in-depth look at reasons to consider a DTP solution. Included in the discussion are concerns with the traditional distribution channels, advantages and challenges...
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Creating and capturing value for outsourcing pharmaceutical manufacturing - Recipharm AB

15-Jul-2013 - An efficient technology transfer process can create value as well as capture it for pharmaceutical companies and CMOs alike.Discover the mutual benefits of working with Recipharm. Because technology transfer has both legal and economic implications, working with an experienced outsourcing manufacturer...
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Endpoint Based Protocol Development: A Central Laboratory Perspective - ACM Global Central Laboratory

20-Jun-2013 - The ability to ensure that relevant and accurate laboratory testing is performed, which will meet the primary and secondary endpoints in a clinical trial, is the basic expectation for any central laboratory. Pharmaceutical and biotech organizations, along with CROs continually...
Watch now!On-Demand Supplier Webinar

Supply Chain Issues and Trends in Asia - Marken

02-May-2013 - Import/export of biological samples from China China: Large Pharma Reverse Logistics A Common Issue: Destruction of Drug in Taiwan J-GMP: How is GMP different in Japan? Korea: Biosimilars Hotbed India: Will Regulations Change to Allow Quicker Study Approval in 2013?
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What Non-statisticians Need to Know about Statistics in Clinical Trials - Rho

04-Apr-2013 - Through real-world examples, webinar participants learn strategies for choosing appropriate outcome measures, methods for analysis and randomization, and sample sizes as well as tips for collecting the right data to answer your scientific questions. 
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Industry Snapshot: Clinical Trial Trends Outline Complexity for Supply Chain - Marken

25-Mar-2013 - 2013 Industry trends driving the scientific, logistical and regulatory complexity of supply chain industry Implement clinical development methodologies for quality, relationships, and performance Strategies to optimize drug development to reduce global trial time and costs
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Working with the cold harsh reality of temperature controlled supply chains - Marken

06-Mar-2013 - What are the regulators telling us? Dealing with a non-harmonized, multi-agency, global challenge.    Monsters Vs, Aliens How to navigate the maze of import & export regulators. Thinking beyond the box! Packaging selection – A different horse for every course Validation & Qualification – Where are...
Watch now!On-Demand Supplier Webinar

Optimizing your Strategy and Budget for Clinical Trial Supply Distribution - Marken

20-Feb-2013 - How to determine if a depot or direct to site shipments are more efficient Calculation based on a case study How to avoid delays and assure that your shipments arrives without delays and excursions
Download now!Technical / white paper

New European Offices, Thermal Packaging Alternatives Accommodate Specialized Needs of World Courier Biopharm Customers - World Courier

11-Feb-2013 - World Courier’s newly-expanded international network − now numbering 152 office locations in 52 countries − brings expertise, personnel and infrastructure closer to key customers in Switzerland and Austria with the recent opening of offices in Basel and Innsbruck.At the same...
Download now!Case study


11-Feb-2013 - VENDOR MANAGED INVENTORYCONTINUED GROWTH IN DEMAND FOR VMI Vendor Managed Inventory (VMI) can be defined as a means of optimising supply chain performance in which a chosen outsourced manufacturer partner is responsible for maintaining their customer’s inventory levels. The manufacturer has...
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The Best of Both Worlds: Swiss Quality, Made in China -

05-Feb-2013 - Lonza brings you the best of both worlds with Swiss quality manufacturing of APIs available at our FDA approved facility in Nansha, China.  From backward integration to tailored production concepts for efficient manufacturing, Lonza offers sustainable solutions for regionally important...

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