With so much uncertainty surrounding the economy, consolidation of pharmaceutical companies, lack of funding for biotechs and drug safety concerns, one thing is for sure – there is still much work to be done to bring new medicines to market and we’re all being asked to do more with less. That’s why it’s imperative to get your clinical outsourced studies right the first time around. And, the long term view from industry experts is that outsourcing will continue to dominate.
But with so much flux in the marketplace due to career shifts, Big Pharma re-orgs and smaller pharma and biotechs ready to send new products into development, there’s a learning curve when it comes to making the right outsourcing decisions. You need to be armed with the information and contacts to get moving - the alternative can cause project delays costing into the millions.
Fundamentals of Clinical Outsourcing is a conference you can’t afford to miss!
→ If you are challenged by making decisions on full-service vs. functional outsourcing, or are struggling to convert a vendor bid into a study contract, you will benefit from the collective experience shared by our expert speaking faculty.
→ If change orders due to hurried or unrealistic scope of work or poor communication with your partners have just about stopped your trial in its tracks, you’ll find solutions for these challenges as well.
→ And, if you’re worried about quality oversight of third party clinical research data, you will hear directly from the FDA on what they expect.
Download the brochure for more information on how to do more with less and get your studies right the first time around.
We understand travel budgets are limited, so we are especially pleased to offer this program regionally in both Boston this October and San Francisco in November to facilitate your attendance.
Make sure to register before August 28th and Save up to $300! Mention Priority code 0T4JXO
We're getting ready to launch a new blog that looks at the broader issues of clinical trials, providing breaking news, insights and strategies into clinical trials business and operations. Update your RSS feed now as we get it ready for our official launch:
http://clinicaltrialpartnerships.blogspot.com/
Web Seminar
Title: Offshoring to Emerging Countries: Navigating Uncertain Waters
Date: Thursday, January 21, 2010
Time: 2:00 PM - 3:00 PM EST
Mention priority code: P1500W2BlogTwitter
Presented by:
Jacquie Mardell
Sr Director Clinical Operations
Metabolex
Sign up for the complimentary webinar here.
Date: Thursday, January 21, 2010
Time: 2:00 PM - 3:00 PM EST
Mention priority code: P1500W2BlogTwitter
Presented by:
Jacquie Mardell
Sr Director Clinical Operations
Metabolex
Sign up for the complimentary webinar here.
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December
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- Central Labs Speaker Profile: Dr. James D Watson
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October
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- PPD Makes Significant Inroad into China Biotech wi...
- Studies may be failing to show adverse effects of ...
- Genzyme begins Phase 3 clinical trial
- Amarin Appoints Medpace as CRO for Two Phase 3 Car...
- Top 5 Clinical Trial Partnering in Asia Pacific Qu...
- Kansas Cancer Center to Join Clinical Trials
- New guidance draft document for REMS
- Adaptive Clinical Trials Benefit Smaller Laborator...
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August
(16)
- Pfizer and Private Team Access Launch New Patient ...
- The lack of participation in clincial trials
- Official Call For Papers: Oncology Clinical Trial...
- Outsourcing of clinical trials expected to rise by...
- Pfizer to create online networking site for clinic...
- Medicare's Stance on Clinical Trials
- Medicare's Stance on Clinical Trials
- Stem cells for the heart in clinical trial
- Biopharma in India is Surging
- goBalto, Matchmaking for CROs and Drug Developers
- India Expected to Take Larger Share of Outsourcin...
- Clinical Trial Cost & Contract Management Agenda F...
- Web Seminar: REMS, EU-RMP and FDAAA: Navigating th...
- Repros Therapeutics Inc. halts clinical trial
- Outsourcing to grow 10% says WSHP
- USA and Europe team together to monitor clinical t...
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December
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