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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR
   
  
EVENTS FOR 2017
   
 
EVENTS FOR ALL MAGAZINES
 
     

RDD Europe 2017

25-28 April 2017
Palais des Congres díAntibes, Nice (Antibes), France

RDD Europe 2017, organized by RDD Online and Aptar Pharma will be held in Nice (Antibes), France, April 25-28, 2017. More>>

 
phone +1 (804) 827-1490
email info@rddonline.com
web www.rddonline.com
email Virginia Biotechnology Research Center 800 East Leigh Street, Suite 206-10 Richmond, VA 23219
 

LogiPharma Europe

25-27 April 2017
Montreux Music & Convention Centre, Switzerland

Now in its 17th successful year, LogiPharma is the largest global end-to-end supply chain event for pharma supply chain leaders, their teams and service partners. More>>

 
web bit.ly/2iENfx4
email Montreux Music & Convention Centre, Switzerland
 

BioProcess International European Summit

25-26 April 2017
RAI, Amsterdam

BioProcess International European Summit is THE Bioprocessing event, bringing together 800+ attendees from all major departments in bioprocessing: Cell Culture, Downstream, Manufacturing, Vaccines, Viral Safety and Cell Line Development. Find out more: https://goo.gl/d64sXs More>>

 
 

World Orphan Drug Congress USA 2017

19-21 April 2017
Washington Mariott Wardman Park, Washington, DC.

THE GLOBAL ORPHAN DRUG CONFERENCE AND EXPO IS BACKOver its 7-year history, the shape of the World Orphan Drug Congress USA has changed from a small conference focused on the US market, to a 4 track event, with over 1,000 global attendees, coming together to discuss the latest trends. More>>

 
phone +1 646 619 1811
email freya.smale@terrapinn.com
web https://goo.gl/1XG74o
email Washington Mariott Wardman Park, Washington, DC.
 

9th Adaptive Designs in Clinical Trials

3-4 April 2017
Copthorne Tara Hotel, London, UK

SMiís annual conference on Adaptive Designs in Clinical Trials will return to London on 3rd & 4th April 2017. Now running for nearly a decade, this unmissable event will gather a senior audience of experts to discuss and deliberate recent innovations and successes in this exciting field of science. More>>

 
phone 0207 827 6000
email events@smi-online.co.uk
web www.adaptivedesigns.co.uk/EBR
email Copthorne Tara Hotel, Scarsdale Place, Kensington, London
 
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Industry Events

Clinical Trial Supply Forum 2018

22-24 January 2018, London, UK

In the constantly changing environment of Clinical Trial Supply, cost efficiency, end to end visibility, logistics and managing complex pipelines are STILL crucial elements that need addressing!
More info >>

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White Papers

Analysis of Biopharmaceuticals to Conform to ICHQ6B

RSSL

Worldwide, the pharmaceuticals market is anticipated to grow from more than USD 782 billion in 2011 to approach a value of just over USD 971 billion by the end of 2016, registering a CAGR of over 24%. In 2010 the average medicines expenditure per person within the UK was £271, and this is expected to increase with the ageing population. A significant and increasing proportion of these sales are protein-based biotherapeutics or biomolecules. Currently, these account for 19% of the total market, and are growing at twice the rate of traditional small molecule pharmaceuticals. It is predicted that close to 50% of the top 100 pharmaceutical products will be biomolecules by 2016. By far the largest segment of the biopharmaceutical market is the monoclonal antibody (MAb) with an estimated share of 25.6%, which corresponds to USD 51.1 billion.
More info >>


News and Press Releases

YHEC announces the promotions of Michelle Jenks and Rachael McCool to the role Project Director

YHEC is pleased to announce the promotions of Michelle Jenks from the Economic Modelling team and Rachael McCool from the Systematic Reviewing team to the role Project Director. Michelle has a Masterís degree (MSc) in health economics from the University of York and has conducted economic evaluations and systematic reviews for both public and private sector clients. Michelle is the lead modeller in YHECís role as an External Assessment Centre for NICE and has also led on a range of economic evaluations conducted for clients within industry, such as cost-utility models and budget impact models. She often leads the development of early economic analyses to inform clinical trial design and pricing strategy.
More info >>

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