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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR
   
  
EVENTS FOR 2017
   
 
EVENTS FOR ALL MAGAZINES
 
     

CPhI Worldwide 2017

24-26 October 2017
Messe Frankfurt, Germany

CPhI Worldwide, together with co-located events ICSE, InnoPack, P-MEC and FDF, hosts more than 42,000 visiting pharma professionals over three days. 2,500+ exhibitors from 153 countries gather at the event to network and take advantage of more than 150 free industry seminars. The exhibition covers every sector of the pharmaceutical market under one roof. More>>

 
email cphi@ubm.com
email Frankfurt, Germany
 

7th annual Orphan Drugs and Rare Diseases UK

18-19 October 2017
Holiday Inn Kensington Forum, London

SMi Group is thrilled to present the 7th annual Orphan Drugs and Rare Diseases conference, taking place on 18th & 19th October 2017 in Central London, UK. This yearís theme will be focused towards discussing strategies for patient engagement, market access and gene therapies to enhance rare diseases and orphan drug research. More>>

 
phone Tel: +44 (0) 207 827 6012
email kwilliams@smi-online.co.uk
web www.orphandrugs.co.uk/samedan
email London, UK
 

LogiMed 2017

18-19 October 2017
Hyperion Hotel, Hamburg

Taking place 18-19th October in Hamburg, LogiMed is Europeís only dedicated medical device supply chain event bringing together over 150 Medical Device Supply Chain Professionals to network with. With a greater focus on customer collaboration and digital transformation this yearís LogiMed delivers real insights on inventory visibility, supply chain planning, global logistics and digitalization. More>>

 
phone 44 (0) 207 368 9766
web bit.ly/2tEaxqD
email Hyperion Hotel, Hamburg
 

BioProduction Congress 2017

17-18 October 2017
Convention Centre Dublin, Ireland

Save the date to attend the 16thAnnual BioProduction Congress; Europeís leading and largest event for a comprehensive update on all aspects of large scale mammalian and microbial biological manufacturing. More>>

 
phone +44 (0) 20 3377 3903
email LS.Registrations@Knect365.com
web bit.ly/2hRw2AU
email Dublin, Ireland
 

8th Clinical Quality Oversight Forum 2017

11-13 October 2017
Sheraton Philadelphia Downtown Hotel, Philadelphia, PA

ExLís Clinical Quality Oversight Forum continues to live up to its reputation as an elite gathering of senior-level executives. More>>

 
phone +44 (0) 20 7724 3456
web bit.ly/2tTxggs
email Sheraton Philadelphia Downtown Hotel, Philadelphia, PA
 

Outsourcing in Clinical Trials Nordics 2017

10-11 October 2017
Copenhagen, Denmark

Enabling local knowledge-sharing, benchmarking and network-building between Nordic biopharma and device industry peers More>>

 
web www.arena-international.com/octnordics
email Copenhagen, Denmark
 
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Industry Events

Pharmaceutical Microbiology East Coast

13-14 November 2017, Renaissance Woodbridge Hotel, New Jersey

Drawing on from the huge success of SMiís Pharmaceutical Microbiology event series, SMi is delighted to announce the launch of Pharmaceutical Microbiology East Coast. Being the eighth in its series, this event will take place in New Jersey, USA, on November 13th and 14th 2017. Aimed at Microbiologists, Quality Control and Quality Assurance Managers, Pharmaceutical Microbiology East Coast 2017 will address the best practices for rapid microbial and sterility testing and tackle the challenges of contamination control.
More info >>

White Papers

Driving ROI: The Case for Investing in Contract & Site Regulatory Document Management Services

DrugDev

With tight timelines and complicated regulatory documentation requirements, getting a clinical trial up and running quickly is easier said than done. Key milestones can be achieved only after the successful negotiation of clinical trial agreements and completion of essential regulatory documents. Many clinical trials are hindered by inefficient, labor-intensive processes. Prolonged, inefficient activation can hamper investigator satisfaction and, ultimately, have a negative bottom-line impact for sponsors and CROs. In addition, the Sunshine Act is heightening the importance of financial disclosure in clinical trials. Without a robust financial disclosure strategy, sponsors cannot ensure that physician self-reported financial disclosure data are aligned with the payment data being reported through the Sunshine Act, increasing financial and regulatory risk.
More info >>


News and Press Releases

GE sets new standard for monoclonal antibody purification: Up to 40% increase in capacity

GE Healthcare introduces a new Protein A chromatography resin, MabSelect PrismA, which will help biopharmaceutical manufacturers improve their monoclonal antibody (mAb) purification capacity by up to 40 percent. The resin is also significantly more alkaline-stable, meaning that MabSelect PrismA can be cleaned with a higher concentration of sodium hydroxide to better control cross-contamination and bioburden risks.
More info >>

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