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Pharmaceutical Manufacturing and Packing Sourcer

pmps
Spring 2018

   
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Industry Insight 
Industry Insight

Randice Altschul, PMPS’s
Industry Advisor, comments on the articles within this edition.
 
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Manufacturing
High-Quality Air in Manufacturing Processes

Air Purity


Maintaining high-quality air during manufacturing can often be a burden for companies, but introducing oil-free compressors can alleviate this, as highlighted by Richard Hilton at Gardner Denver.
 
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Cool Chain, Cargo & Logistics
Spotlight

Aiding Pharma in Airfreight

Ludo Claes at Krautz-TEMAX explains how a thermally engineered blanket can be used to ease constraints encountered with temperaturesensitive pharmaceuticals in an airfreight cold chain.
 
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Formulations, Ingredients and Excipients
Orally Disintegrating Tablet Challenges

Dissolvable Development


Dr Carolina Diaz Quijano at Omya International demonstrates how functionalised calcium carbonate improves compatibility and disintegration time in orally dispersible tablets.
 
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MANUFACTURING
CMO Research in Slovakia

Optimising Outsourcing

Markus Saal at Saneca Pharma explains how outsourcing to Slovakia may be a way to drive business for contract partners in Central and Eastern European countries, given its profitable market.
 
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PREVIEWS & REVIEWS
Event Preview

FlyPharma Europe Touches Down in June


The FlyPharma Conference Europe returns again this year, taking place on 5-6 June in Brussels, Belgium.
 
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CLINICAL TRIAL SUPPLIES & LOGISTICS
Smart Packaging

Context is King


Tom Lawrie-Fussey at Cambridge Design Partnership explores the potential of smart packaging, suggesting it has many benefits including its use in clinical trials and drug efficacy.
 
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COLD CHAIN TECHNOLOGIES & SHIPPING
Temperature-Sensitive Product Logistics

Cold Conditions

Shipping temperature-sensitive products is challenging, and passive packaging systems could alleviate these pressures around cold chain requirements, as illustrated by Softbox SystemsClive Bryant and Richard Wood.
 
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Thermal Protection Solutions

Protective Packaging

Kevin Valentine at TP3 Global and Cool Logistics India advises on factors to consider when selecting thermal protection covers to ensure seamless distribution of temperature-sensitive pharmaceuticals.
 
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Supply Chain
Traceability and Serialisation Challenges

Supply Network

Pasi Kemppainen at Santen Pharmaceutical outlines the three pillars of integration and interoperability that businesses should consider to optimise serialisation and traceability.

 
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DIGITAL Supply Chain
Improving Security and Performance

Digital Double-Win

Dr Evren Ozkaya at Supply Chain Wizard comments on the risks that can come with digital supply chains and the best ways to manage production efficiency in this area.

 
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The End of the line
End of the Line

The Deal Structure


PMPS Industry Advisor Randice Altschul outlines some of the licensing challenges that companies may encounter when producing a therapeutic and how best to approach them.
 
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Anti-Counterfeiting and Serialisation
Q&A: The Falsified Medicines Directive

Controlled Conduct


As the introduction of the new Falsified Medicines Directive approaches, Accord Healthcare’s Sandra Lee tells PMPS why serialisation is important and how the industry can prepare for the changes.
 
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Open Serialisation Communication Standard

Fight Against Counterfeit


Drugs Given the need for stricter regulations to combat counterfeit drug sales, Gaurav Mohite at ACG Inspection Systems introduces a new product serialisation method that aims to combat the issue.
 
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Serialisation and Late-Stage Customisation

Time is Short


Atlantic Zeiser’s Stefan Rowinski explores the benefits of late-stage customisation ahead of the introduction of new serialisation and labelling standards being enforced in the EU.
 
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Preventing Counterfeiting Through Regulations

Seamless Serialisation


Mark Davison at rfxcel claims that a number of factors should be considered when implementing serialisation technology, which should be done before regulators remove the right to trade.
 
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Q&A: The Future of Serialisation

Supplying Success

In light of the upcoming EU serialisation regulations, Erik Haeffler at Recipharm, Carlos Machado at SEA Vision, and Dexter Tjoa at Tjoapack lend their expertise through a roundtable discussion on how it can best be applied.

 
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Counterfeiting Challenges

Traceable and Transparent

The pharma industry’s ongoing battle with counterfeiting could be remedied through transparent supply chains to stop drug theft. Julie Hurley at Unisys discusses how this approach could ensure patient safety.
 
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Published quarterly in
February, May,
August, and November

News and Press Releases

Recipharm Invests in its Single Dose Nasal Platform Capabilities

 Recipharm, a global contract development and manufacturing organisation (CDMO), has announced that it is expanding its capabilities for its proprietary Unidose® Xtra (single dose) nasal delivery platform.
More info >>

White Papers

What is process characterization?

EXPUTEC

Process characterization is an essential step in the commercialization of a new (biological) drug. For drug product commercialization, manufacturers must validate the drug’s manufacturing process. This ensures that the manufacturing process delivers consistently a quality product and that the patient is not at risk.
More info >>

Industry Events

The Pharmaceutical Manufacturing and Packaging Congress 2023 (PHARMAP 2023)

12-13 June 2023, Hilton Geneva Hotel & Conference Centre, Geneva, Switzerland

The Pharmaceutical Manufacturing and Packaging Congress 2023 (PHARMAP 2023) gathers top-level management from pharmaceutical companies of manufacturing, primary and secondary packaging, purchasing, and supply chain and procurement sectors, CMOs and CDMOs leaders, heads from government and institution on 12-13, June, 2023 in Geneva, Switzerland.
More info >>

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