Symposium: Monitoring Safety in Clinical Trials and Drug Development
Dates: 27th and 28th February 2008
Venue: Southampton
Monitoring, reporting and analysing safety in clinical trials are important functions. Staff working in a range of disciplines need to know about the regulatory, legal, clinical and other aspects of safety in clinical trials. The implementation of the Clinical Trial Directive was a critical event for clinical research and pharmacovigilance which impacted on all those working in pre-registration clinical research or in clinical trials.
The DSRU as one of the leading providers of education and training in pharmacovigilance in Europe, will be holding a Symposium on this important topic. Join the DSRU and invited speakers for this high quality, exceptionally good value Symposium and hear directly from those involved about how the legislation is being interpreted.
Statutory GCP Inspections of Clinical Laboratories Conference
Date: 5th March 2008
Venue: McDonald Burlington Hotel Birmingham
Is your company ready for a statutory laboratory inspection?
Everything you need to know about inspections of clinical laboratories - before, during and after.
A comprehensive one day conference providing guidance on the inspection process.
Learn how to identify compliance issues, organisational guidance and identify common problems
Gain insight into sample tracking; the use of LIMS system
Identify issues associated with informed consent, un blinding and re blinding of studies
Understand patient confidentiality
Hear first hand role and responsibilities of key personnel
Improve data reporting
Two-Day National Conference on Biotechnology & Clinical Research in India
Dates: 7th - 8th March, 2008 at J.N. TATA Auditorium,
Indian Institute of Science - Hosted by ICBio.
Last date for registration & submission of abstract is 15th Feb.2008
Conference registration is available online from our website, **
www.icbio.org. if you are interested to
participate in the conference, please take the print out of the registration
from and fill it send to us by post along with registration fee
Rs. 400/- for students
Rs. 800/- for faculty
Rs. 1500/- for researcher / corporate staff employee For more details please
feel free to 9900121064 or mail to us at
conference@icbio.org.
This event is sponsored by Dept. of IT&BT, Govt. of Karnataka
Co sponsored : Chembiotek Research International Ltd
Assocate sponsor: Metaome Science Informatics Pvt. Ltd,
Media partner : - FM Rainbow, Biospectrum ( Biotech magzine)*
China 2008 R&D Summit
Dates: March 31 – April 2, 2008. Grand Hyatt Hotel. Shanghai, China
Session include
Trends & Outlook of China’s Pharma & Biotech Industry for the Next Five Years
China’s Top Scientists – Recognizing the Leaders in Advancement of Science & Technology and their Achievements/Contributions in China
Global Pharma Exchange Round Table Discussion
Research & PreClinical Track Drug Discovery in China – Case Studies of Licensing & Partnering in Research in China
Clinical Development Track Clinical Research Development in China – Experiences, Improvements and Changes
Panel Discussion: Intellectual Property Rights – Protecting & Defending your Patents
VC/Investment Round Table – Valuations, ROIs and Exit Strategies
Innovation Showcase
Exploring China’s Scientific Advantages
Biologics (Biogenerics/Bio-improvements/Proprietary Proteins)
TCM-based Drug Discovery
For More Information, visit www.IBCLifeSciences.com/china
29th ICR Annual Conference and Exhibition 2008
Communication in Clinical Research; Challenges in a complex world
Venue: The ICC, Birmingham, UK
Dates: 8th and 9th April 2008
Discover the secrets behind media coverage of science
Get udated on regulations from competent authorities
Begin tackling the lifestyle diseases of tomorrow.
Learn how to operate effectively in a global workplace
Discuss the impact of changes in the ethics environment
Meet your peers and make new contacts
See latest developments & check out competitors at the biggest clinical research exhibition in Europe
Clinical IT Systems Europe 2008
Validating Clinical IT Systems: Dates 28th and 29th April 2008
Auditing Clinical IT Systems: Date 30th April 2008
Venue: Hilton Olympia Hotel, London, UK
Includes interactive workshops and real case study examples
Free Book! Every attendee will receive a free copy of the ACDM's Practical Guide titled "Computerised Systems Validation in Clinical Research".
Some of the topics include:
Computerised systems used in clinical R & D, Interfacing with IT Department, Security and Access Control for GCP Systems, Hospital Computerised Systems & CRO's, FDA's New Guidance for Computerised Systems Used in Clinical Investigations, Risk based validation and testing approaches to global IT system projects, Planning a Clinical IT System Audit, Auditing the developing clinical system etc...