Clinical Trials

(44 results)(Back to Archives)

*How to investigate environmental monitoring excursion limits
Palo Alto, United States
10 Dec 2010 - 10 Dec 2010
This environmental monitoring training will review the best practices for setting environmental monitoring alert and action levels for viable and non-viable data including product bioburden.

*How to secure GCP compliance in Clinical Trials
Palo Alto, United States
23 Nov 2010 - 23 Nov 2010
This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense..

*Conducting Clinical Trials in Latin America
Palo Alto, United States
22 Nov 2010 - 22 Nov 2010
This Clinical trial training will review the current status of Clinical Trials activities in Latin America, the factors that make this region such an attractive one and some best practices to ensure a successful implementation of clinical trials..

*Are you a new Clinical Research Coordinator? Tips on how to get started
Palo Alto, United States
17 Nov 2010 - 17 Nov 2010
This clinical research webinar will discuss the role and responsibilities of an efficient well rounded Clinical Research coordinator and what to do pre and post trial period to comply with GCP and other regulations..

*Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
Palo Alto, United States
19 Oct 2010 - 19 Oct 2010
This adverse event reporting Webinar/training will discuss the clinical trial regulations requirements with respect to adverse event and explain how to assess and report AEs and SAEs..

*The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Palo Alto, United States
5 Oct 2010 - 5 Oct 2010
This GCP training Webinar will discuss the principals of GCP, the regulations pertaining to it and elements necessary for FDA compliance..

*How to Use Foreign Trial Data in Your NDA Approval Process
Palo Alto, United States
28 Sep 2010 - 28 Sep 2010
In this NDA Approval Process training Webinar learn the guidance and regulations governing FDA’s acceptance of foreign trial data and know how FDA implementing these rule along with design considerations and requirements for foreign trials..

*Navigating Pediatric Trials from recruitment to successful on-time completion
Palo Alto, United States
16 Sep 2010 - 16 Sep 2010
In this Pediatric Trials training learn how to evaluate the current issues and best practices in pediatric drug development, clinical investigation of medicinal products and non clinical evaluation of pediatric drug products..

*Vendor selection in clinical trials, assessment activities, audits and log of preferred partners
Palo Alto, United States
2 Sep 2010 - 2 Sep 2010
In this Clinical Trial training learn about clinical trial Vendor Assessment, Project Management, Outsourcing, and Trial Design..

*How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Palo Alto, United States
26 Aug 2010 - 26 Aug 2010
In this CLIA inspection webinar understand how to get your lab ready for inspection, what the inspectors will look for and how to do inspection follow up and response..

*Fundamentals of FDA’s Clinical Trial Audits – A Must- Know for Audit preparation
Palo Alto, United States
24 Aug 2010 - 24 Aug 2010
This Clinical Trial Audits webinar will provide help both CRAs and sites utilize quality improvement methods and effectively prepare for upcoming GCP audits..

*Defining and Managing Protocol Deviation/Violation/Exception
Palo Alto, United States
10 Aug 2010 - 10 Aug 2010
In this GCP Webinar training, learn how to proactively predict and manage Protocol Deviation/Violation/Exception. Understand the guidance for implementation of “Protocol Not Followed” (PNF)..

*The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Palo Alto, United States
10 Aug 2010 - 10 Aug 2010
This ICF process Webinar training teaches how to create an informed consent process for achieving optimal site compliance and subject comprehension. It also discusses how an inadequate ICF can affect data integrity and patient safety and/or well-being..

*Outsourcing Clinical Trials in Latin America
Palo Alto, United States
12 Aug 2010 - 12 Aug 2010
This clinical trial training will review some Outsourcing Models that have been used successfully in the Latin American countries where Clinical Research is developed,.

*How Accurate Adverse Event Reporting is the Key to Subject Safety of approved drugs
Palo Alto, United States
4 Aug 2010 - 4 Aug 2010
In this Clinical compliance training learn how to assess record and manage the adverse events occurring during conduct of clinical research utilizing human subjects and how to avoid the common mistakes..

*Auditing vs. monitoring, defining the purpose, application and process
Palo Alto, United States
3 Aug 2010 - 3 Aug 2010
In this Clinical Trial audit training learn risk-based approach to the process of monitoring and auditing clinical trial..

*Safety Pharmacology World Europe
London, United Kingdom
28 Sep 2008 - 30 Sep 2008
Safety, Pharmacology, Drug, Cardiovascular, Pharmacovigilance, Pharmaceutical, Strategy.

*Oncology Leaders' Forum 2007
Boston, MA, United States
14 Nov 2007 - 16 Nov 2007
Defining the oncology therapeutics marketplace of 2017 - what are the key strategic decisions that your organization must make today to meet the future demands of regulator, payer, physician and patient?.

*5th Canadian Annual Meeting: Blueprint for an Evolving Regulatory Environment
Ottawa, ON, Canada
28 Oct 2007 - 30 Oct 2007
Issues of Interest Facing Health Canada, the Pharmaceutical Industry, Health Academia, and the Health Care System.

*Publication Planning Forum
Philadelphia, PA, United States
27 Sep 2007 - 28 Sep 2007
Our 2007 program provides key solutions for successfully utilizing publication planning as a launch pad for a strong commercial rollout despite regulatory roadblocks and deadline setbacks from journals.

*4th Latin American Congress of Clinical 4th Latin American Congress of Clinical Research
São Paulo, SP, Brazil
27 Sep 2007 - 29 Sep 2007
Global Initiatives of Clinical Research in Latin America.

*Rosenön Meeting 2007: DMPK and PK/PD from Lead to Product - Recent Developments and Trends in an Expanding Science
Stockholm, Sweden
20 Sep 2007 - 22 Sep 2007
This years Rosenön meeting will present the most recent scientific and strategic advancements in preclinical DMPK and PKPD and its application throughout the various discovery and development stages..

*Clinical Trials - Beyond Borders
Zurich, Switzerland
27 Sep 2007 - 28 Sep 2007
Clinical Trials - Beyond Borders will explore many aspects of clinical trials in Eastern Europe and Asia. There will be in-depth discussions on the benefits and drawbacks of conducting trials in these regions etc..

*Targeted Designs for Clinical Trials
Philadelphia, PA, United States
19 Jul 2007 - 20 Jul 2007
Learn from leading experts on how to accelerate the path to drug development, lower your clinical trial costs and improve your study`s therapeutic ratio of benefit to adverse effects..

*"Methods in Clinical Cancer Research"
Flims, Switzerland
23 Jun 2007 - 29 Jun 2007
FECS, AACRand ASCO have responded to this problem by designing jointly a programme that will: Introduce junior clinical oncologists in any oncology subspecialty to the principles of good clinical trials design etc..

*China 2007 R&D Summit: Partnering, Licensing & Outsourcing from R&D Clinical Trials
Shanghai, China
4 Jun 2007 - 6 Jun 2007
The event offers a platform for international companies to better evaluate the cost savings in perspective of the quality and capabilities of the Chinese companies, while at the same time, solidifying their strategies.

*Allan Lloyds` Optimizing Clinical Trials 2007
Amsterdam, Netherlands
30 May 2007 - 31 May 2007
This Conference is a designed platform targeting the most relevant issues, current trends, future perspectives in clinical trials within the pharmaceutical industry. Learn and gain thorough understanding of the present challenges..

*Adaptive Designs for Clinical Trials
Cambridge, MA, United States
10 May 2007 - 11 May 2007
Strategies, Methods and Logistical Considerations for Flexible Trial Designs.

*19th ACCP Frontiers Symposium
Baltimore, MD, United States
30 Apr 2007 - 1 May 2007
Innovative Approach for Early Drug Development - Disease Models and Novel Trial Design.

*Clinical Research and Product Registration of Biopharmaceuticals/Vaccines in India and China
San Diego, CA, United States
26 Apr 2007 - 27 Apr 2007
India and China, two of the world’s most populous countries and once considered difficult markets to enter, have taken significant strides as emerging markets in drug development..

*Drug Discovery and Development Partnering, Licensing and R&D Innovation Summit JAPAN
Tokyo, Japan
25 Apr 2007 - 27 Apr 2007
The ONLY international conference in Japan providing multiple speaker case studies of successful international alliances and R&D strategies PLUS themed networking events to help you find partners and meet new companies from Japan, USA, Europe and Asia..

*Industry and Health Authority Conference on: Oligonucleotide-based Therapeutics
Bethesda, MD, United States
19 Apr 2007 - 20 Apr 2007
This conference will establish dialogue and discussion among Industry and Health Authorities to inform, teach, and share product development and regulatory information in the areas of nonclinical, chemistry, manufacturing and control (CMC) etc..

*CHI's Molecular Medicine Tri-Conference
San Fransisco, United States
27 Feb 2007 - 2 Mar 2007
Bridging: Biology , Chemistry , Business.

*Bioanalysis in Clinical Research
London, United Kingdom
21 Feb 2007 - 22 Feb 2007
We are bringing you the 2nd Annual Bioanalysis in Clinical Research Summit, focusing on the latest regulations, methods and technologies to help you to become more efficient and to avoid product failures..

*Creating Strategic & Regulatory Compliant Phase IV Studies
Hallandale Beach, FL, United States
27 Feb 2007 - 28 Feb 2007
One of the key strategies in successfully conducting a clinical trial is to work with key opinion leaders & key thought leaders in the field to assure that the product gets out to market & that you are able to attract as many people into the trial as poss.

*Developing Clinical Research Hubs in Asia
Singapore, Singapore
26 Feb 2007 - 27 Feb 2007
Raising the standards of clinical trials in Asia through harmonising regional clinical research operations..

*8th Annual Phase I Clinical Trials: Improving safety, reducing costs and increasing efficiency in Phase I studies
London, United Kingdom
19 Feb 2007 - 22 Feb 2007
Save money, improve safety and increase efficacy in your Phase I clinical trials; Understand the consequences of the TeGenero experience on phase I trials;Avoid product failure by learning exactly how to satisfy your regulators.

*Clinical Trials Congress 2007
Las Vegas, NV, United States
6 Feb 2007 - 8 Feb 2007

San Fransisco, United States
5 Feb 2007 - 6 Feb 2007
This course provides pharmacovigilance personnel with the tools to remain compliant, and the knowledge of what needs to be reported when and to whom..

*Recombinant Therapeutics
Berlin, Germany
29 Jan 2007 - 31 Jan 2007
In the light of the adverse immunological effects that TGN1412 evoked fundamental points of concern have arisen. This conference will address these points..

*Biostatistics for Non-Statisticians
Malvern, PA, United States
3 Jan 2007 - 5 Jan 2007
This course is designed as an introduction to the statistical principles that form the basis for the design and analysis of research investigations. The focus of topics will benefit individuals within the pharmaceutical and biotech industries.

*Monitoring Clinical Drug Studies: Beginner
Boston, MA, United States
18 Dec 2006 - 20 Nov 2006
This is a basic how to workshop with a strong grounding in current regulatory requirements designed for entry level monitors with less than one year of experience..

*Latest Developments in Gene Therapy
London, United Kingdom
26 Sep 2006 - 29 Sep 2006
Now is the time to focus on gene therapy. Following developments with inherited diseases, the industry is preparing to exploit this new technology. An increasing number of products are entering clinical trials for cancer, neurological etc..

*4th Annual Patient Recruitment for Clinical Trials
New York City , NY, United States
13 Sep 2006 - 15 Sep 2006
Clinical trials are the costliest & most time-consuming phase of drug development, claiming the bulk of the $51.1 billion invested in research and development by pharmaceutical and biotechnology companies in 2005, according to the Pharmaceutical Research.

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