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home > pmps > Autumn 2008

PUBLICATIONS

Pharmaceutical Manufacturing and Packing Sourcer

Autumn 2008

At the cutting edge of the latest industry developments, Samedan is adept at keeping the information you need at your fingertips. PMPS provides a unique platform of communication for the market across Europe, North America and the rest of the developed world. To find out what's hot in the world of pharmaceuticals, take a look below at the range of articles featured in this issue of PMPS.

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Manufacturing

Brian Dougherty of SCM Pharma Ltd suggests that it is time to seek out new ways to capitalise on innovation in the clinical manufacturing sector

Felix Nink at Bosch argues that automation and modular design are radically changing how pharmaceutical processing looks at containment

Benoоt Verjans of Aseptic Tech introduces closed vial technology: a new methodology for aseptic filling of injectable drugs

Kevin Menard at PerkinElmer Life and Analytical Sciences cites hyphenated techniques as the next generation in laboratory advancements for the pharmaceutical industry

Getting a potential new drug or product from the research and development stage into use has to be the key commercial consideration for pharmaceutical companies. Mark Perry from Siemens Automation and Drives explains how embracing manufacturing execution systems (MES) can have a real impact in an industry when every day counts towards financial success

Drug Delivery

Dr Renaud Janssen at Helvoet Pharma examines the use of silicon in the manufacture of pre-filled syringes, and details its importance in the production of a safe, high-quality product

François Dessus and Flore Demay at Stelmi discuss how to ensure the highest degree of assurance in the production of rubber stoppers sterilised by gamma irradiation

Cedric Marmonier at Rovipharm traces the development of liquid drug administration from the spoon to the syringe, and examines possible future development

Paul Kippax of Malvern Instruments and David Morton of Monash University assess the benefits of using dry powder inhalers in order to optimise the delivery of a wide range of medicinal drugs

Ed Wynn at ANSYS analyses the impact of computational fluid dynamics on pulmonary drug delivery

Formulations, Ingredients and Excipients

Kevin Maynard at Imprint Pharmaceuticals and Victor Breedveld from the Georgia Institute of Technology discuss particle tracking microrheology

Partnerships between pharma and excipient manufacturers can extend drug patents through novel functionalities and formulations; Hans Huttinga at Sheffield Pharma Ingredients investigates

IT and Logistics

Leigh Jordan at Cognex UK Ltd identifies machine vision and coding as essential ingredients of an efficient traceability strategy

Chris Stumpf and Phil Kilby at Waters discuss lean process improvements for the GMP laboratory

PACKING, PACKAGING & ANTI-COUNTERFEITING

Benjamin Kepp of Bischof + Klein GmbH discusses how flexible packaging can solve contamination problems across the whole drug development process

John Gill at the Royal National Institute for the Blind discusses what can be done by pharmaceutical packagers to help blind and partially sighted people

Gerhard Breu at Körber Medipak explains how the bar in patient compliance can be raised through box wallet packaging

With pharmaceutical labelling becoming increasingly regulated, manufacturers and packaging companies are looking for a simple and cost-effective solution. Mark Beauchamp at Citizen Systems Europe explains that the latest generation of label printing technology can meet both requirements

Paul Stiff at Farnham Castle International Briefing Centre examines the inherent difficulties in recognising international commercial needs in packaging and manufacturing

COOL CHAIN

Geraint Thomas at Laminar Medica explains how the latest temperature-controlled packaging technology is helping pharmaceutical companies meet the growing challenge of shipping temperature-sensitive products

Chris Fore at Envirotainer presents strategies to meet transport service provider obligations as defined in Parental Drug Association Technical Report Number 39

In the current financial climate, making the correct choice when selecting chillers and air conditioning systems is more important than ever; Steve Warnock of the Coolmation Group explains why the sector should consider Turbocor compressor chillers when reviewing climate control

Tony Wright at Exelsius Cold Chain Management Consultancy examines cold chain management, and tells us it is key to securing both patient safety and the quality of pharmaceutical products

Tim Jennings of Emball’iso SA talks to PMPS about the expanding cold chain sector of the pharmaceutical industry

Edited by
Randice Altschul
Chief Executive Officer at Pop Test and Palisades Therapeutics

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August and November

News and Press Releases

rfxcel Covers the Cost of EMVO Onboarding Fees

May 23, 2018 - San Ramon, CA – rfxcel Corporation, a technically certified Gateway Provider for the European Medicines Verification Organisation (EMVO) announced today that it will pay the cost of statutory fees payable to EMVO* for all manufacturers (Marketing Authorisation Holders, MAHs) which select rfxcel as their Gateway Provider before June 15th 2018.
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White Papers

Life Cycle of an Analytical Method - a Case Study on the Monocyte Activation Test

Wickham Laboratories Limited

Pyrogens, a heterogeneous group of fever inducing contaminants, are comprised of microbial and non-microbial compounds; e.g. endotoxin (lipopolysaccharide, LPS) produced by Gram-negative bacteria, lipoteichoic acid (LTA) from Gram-positive bacteria, bacterial DNA (CpG-motive), endogenous pyrogens, virus and fungi particles or even fragments of packaging materials, plastic and dust. Contaminat ion wi th pyrogens in pharmaceutical products, biotherapeutics and on medical devices can lead to life threatening fever reactions. To ensure consumer safety, pyrogen testing is mandatory for parenteral products and medical devices.
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Industry Events

PDA Universe of Pre-Filled Syringes and Injection Devices

8 October - 9 November 2018, Loews Royal Pacific, Orlando, FL

At the 2018 PDA Universe of Pre-filled Syringes and Injection Devices,industry and regulatory experts will share experiences, new developments, regulatory considerations, challenges, and industry trends and best practices. This is a must-attend event for all industry professionals involved in the development, manufacturing, testing, or marketing of pre-filled syringes and injection devices.
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