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resDNASEQ® E. coli Residual DNA Quantitation System

Integrated sample preparation and real-time PCR assay for the quantitation of E. coli host cell DNA.

  • Highly sensitive quantitation using proven TaqMan® real-time qPCR technology (Figure 1)
  • Manual and automated sample preparation, optimized for quantitative recovery from complex sample matrices (Table 1)
  • Enables consistent performance across the expected range of DNA fragment sizes (Figure 2)
  • Integrated system from sample to results with sample preparation, master mix, TaqMan® primer/probe mix, and genomic DNA standard

To learn more, click here >>

Featured whitepaper

Good weighing practices for the pharmaceutical industry
Author: Mettler-Toledo

In the laboratory, weighing is only one step of a whole analysis chain in drug discovery and quality control; however it strongly influences the overall quality and integrity of the final result. Also in production, weighing is decisive to achieve batch uniformity and consistency, e.g. in dispensing or formulation processes. Proper weighing is thus essential to ensure continuous adherence to predefined process requirements and to avoid a frequent source of Out of Specification results (OOS).

Download >>

Whitepapers available for download:

Uniform and Scalable EB Formation for Drug Discovery and Regenerative Medicine Applications
Author: STEMCELL Technologies

Whitepaper: New Support for ISO 14644-1
Author: HACH LANGE

A comparison of the attributes of the AccuGENX-ID microbial sequencing methods versus MicroSEQ v2.0
Author: Accugenix

Autoantibody biomarker panels for improved disease diagnosis
Author: Oxford Gene Technology

An Interview with Dr. John Rossi
Author: Integrated DNA Technologies

RNA-Seq Data Comparison with Gene Expression Microarrays
Author: illumina

The importance of being profiled: Improving drug candidate safety and efficacy using cross-target profiling
Author: Merck Millipore

Company Directory

Premium & Premium+ listings:

- ABB Analytical Measurements
- Almac
- Azbil BioVigilant, Inc.
- B&W Tek, Inc.
- BASF
- Bio-Optronics, Inc.
- bioMérieux
- Bruker Optics
- CAMO Software AS
- Catalent Pharma Solutions
- Chemspec Europe Ltd
- CI Precision
- Cisbio Bioassays
- Dow Chemical Company Ltd
- DSM Biologics
- EMD Millipore
- FOSS NIRSystems, Inc.
- GE Analytical Instruments
- GenScript USA Inc.
- Gerresheimer Group
- HACH LANGE GMBH
- HORIBA Scientific
- I Holland Limited
- IDBS
- Lonza
- Merck Millipore
- MPI Research
- Pall Life Sciences
- Patheon Inc
- Phenomenex
- Porvair Sciences Ltd
- Randox Pharma Services
- Rapid Micro Biosystems
- Realia
- Roche
- rommelag®
- Siemens AG
- Sirius Analytical Instruments Ltd
- Umetrics

Add your company here

Society of Biology

The Society of Biology is the largest professional body for the biological sciences in the United Kingdom – representing over 11,500 individual life scientists and 90 member organisations. Membership of the Society will help you stay up to date with what is happening across the life sciences and provide you with additional recognition for your skills and experience. Members can become Chartered through the Society and we offer two professional awards: Chartered Biologist (CBiol) and Chartered Scientist (CSci). Which award is best for you depends on your particular job role, circumstances and personal self-identification as a biologist or a scientist.

Click here for more information about the benefits of membership >>

AstraZeneca appoints Roche COO as CEO

AstraZeneca have announced today that Pascal Soriot has been appointed as the company’s Chief Executive Officer. Pascal Soriot will take on his new responsibilities and join the AstraZeneca PLC Board as an Executive Director on 1 October 2012. A French national, 53 year old Pascal Soriot joins AstraZeneca from Roche AG where he has served as Chief Operating Officer of the company’s pharmaceuticals division since 2010.

Read full story >>

  Pascal Soriot

More pharmaceutical & life science news

Changes to the Roche Corporate Executive Committee
Daniel O’Day appointed new Head of Roche Pharma– Roland Diggelmann will assume the position Head of Roche Diagnostics...

Lundbeck receives approval from Health Canada for Treanda®
Lundbeck announced that Health Canada has approved Treanda® following the success of the brand in both Europe and the US...

Novartis drug Jakavi® first medication to receive European Commission approval to treat patients with myelofibrosis
Novartis received approval today from the European Commission for Jakavi®...

European Commission approves ZINFORO™ (ceftaroline fosamil) for adult patients with serious skin infections or community acquired pneumonia
European Commission approves ZINFORO™...

U.S. FDA approves Gilead’s Stribild™
Gilead Sciences, Inc. announced that the U.S. Food and Drug Administration (FDA) has approved StribildTM...

Clinical experience with Pradaxa® crosses one million patient-years of treatment
40,000 people estimated to be saved from a stroke related to non-valvular atrial fibrillation...

Key results from new tiotropium studies in COPD and asthma to be presented at ERS 2012
New data to be presented at the Annual Congress of the ERS 2012...

New data from Phase III EMILIA study showed Roche’s trastuzumab emtansine (T-DM1) significantly improved survival of people with HER2-positive metastatic breast cancer
Pivotal study met co-primary efficacy endpoint of overall survival...

Daiichi Sankyo and Lilly Announce TRILOGY ACS Results Regarding Effient® (Prasugrel) in Acute Coronary Syndrome UA/NSTEMI Patients to be Managed Medically without an Artery-Opening Procedure
Study did not meet primary objective of demonstrating prasugrel superiority over clopidogrel in this patient population...

Merck provides update on cardiovascular development program
Merck provided an update on the development programs for vorapaxar, extended release niacin/laropirprant and anacetrapib...

New Novartis Phase II data show LCZ696 may provide clinical benefits in patients with a difficult-to-treat form of heart failure
Novartis announced results from the Phase II PARAMOUNT study...

Handheld Raman: Cut costs, improve efficiency & move toward 100% testing

In this one hour instructional webinar we will discuss how handheld Raman reduces costs and improves efficiency, the move to mandatory 100% testing of incoming raw materials, and recent developments in handheld Raman technology:

  • The move to mandatory 100% testing of incoming raw materials
    Ravi Kalyanaraman PhD, Principal Scientist, Bristol Myers Squibb
  • How handheld Raman improves efficiency
    John Kauffman, Research Chemist at FDA

Find out more >>


Conferences, events & exhibitions:

Genomics Research Europe
4 - 5 September 2012 Frankfurt, Germany

ELRIG Drug Discovery 2012
5 - 6 September 2012 Manchester, UK

HUPO 11th Annual World Congress
9 - 12 September 2012 Boston, USA

Design Control for Medical Device Professionals
10 - 11 September 2012 Berlin, Germany

Design Validation, Verification, and Risk Analysis for Medical Device Professionals
12 - 13 September 2012 Berlin, Germany

Validation of Computer Systems
17 - 18 September 2012 Dublin, Ireland

The EU Clinical Trial Directive
17 - 18 September 2012 Dublin, Ireland

ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
17 - 19 September 2012 Dublin, Ireland

The Drug Development Process – From Discovery to Commercialisation
19 - 21 September 2012 Dublin, Ireland

11th Annual Biological Production Forum 2012
24 - 26 September 2012 Dusseldorf, Germany

MipTec 2012
24 - 27 September 2012 Basel, Switzerland

Lab-on-a-Chip World Congress
25 - 26 September 2012 San Diego, USA
 


Industry Reports:

The “Patent Cliff”: How Pfizer has responded to the loss of its best-selling drug
The global pharmaceuticals market was worth $733bn in 2010. With the patents of many of the world’s best-selling drugs expiring, the market is currently in the middle of a “patent cliff”. This Case Study looks at the various routes companies are taking in order to minimize the adverse effects caused by this “patent cliff”.

OTC Pharmaceuticals: Global Industry Almanac 2011
OTC Pharmaceuticals: Global Industry Almanac is an essential resource for top-level data and analysis covering the OTC Pharmaceuticals industry. It includes detailed data on market size and segmentation, textual analysis of the key trends and competitive landscape, and profiles of the leading companies. This incisive report provides expert analysis on a global, regional and country basis.

Johnson & Johnson Case Study: Remicade, a Biotech Blockbuster
Remicade is a drug used in treating a variety of immune system diseases, and its active ingredient is produced through biotechnology. Johnson & Johnson reported Remicade sales of $4.6bn in 2010, and the drug is the best-selling “biologic” in the world. This case study examines its long journey from an academic research laboratory to a leading position in the pharmaceutical market.