Cliniminds www.cliniminds.com, announced one more workshop on Clinical Trial Auditing & Inspections to be held on 16th -17 th January 2010 in Bangalore after getting huge response from previous workshops.
Clinical Trials in India have increased exponentially in number over the last decade. The increased business has brought into sharp focus the need to manage quality while conducting clinical trials. Clinical trial being the most costly and time-consuming elements of product development if any procedural errors render unusable the information gathered in a series of clinical trials, the time and expense required to conduct the studies again can easily terminate the entire development effort. This workshop is specifically designed for those involved in preparing for and overseeing GCP inspections and those responsible for quality assurance and auditing in the industry.
An audit of a clinical trial provides the research sponsor with independent appraisal of the quality and completeness of the data generated by the trial. Although auditing alone cannot transform a poorly planned, executed, monitored, or analyzed trial into a credible one, an active clinical trial audit program will point out potential problem areas early, so solutions can be found before it is too late. Used effectively, therefore, audits can reduce costs, maintain project schedules, and ensure regulatory compliance.
Cliniminds has successfully conducted several other workshops under the domain of Clinical Research and this time Cliniminds introduce Mr. Paul Benninger as a key note speaker .Mr. Paul Benninger has twenty years of global Clinical and Bio analytical research experience; the last 10 years have been in the pharmaceutical CRO sector which has included full P&L responsibility for business units in Canada (Toronto) and the US (Miami). He has been involved in numerous successful North American FDA and TPD inspection as well as providing independent auditing services for Indian CROs. In 2006 while under his leadership, Allied Research International was named one of the 50 Best Managed Companies in Canada. Other speakers are Mr.Aswani Pandita ,Dr. Naveen Tirkey and Mrs.Deepti Goel.
Mr.Aswani Pandita having 7 years of experience and working with Reliance Life Sciences Pvt. Ltd. (RLS) as Deputy Manager - Clinical Quality. Dr.Naveen is a Certified Clinical Research Associate (CCRA) from Association of Clinical Research Professionals (ACRP) and a pharmacologist (Ph.D.) by education with broad experience (around 9 years) together in Clinical Research as well as academics for drug development processes and Mrs Deepti Goel has over 9 years of experience in clinical research working with Pharma companies, CRO and training academy.
The aim of the workshop is upon completion, participants would be able to understand the concepts of quality assurance in clinical trials; process and implications of Audits & Regulatory inspections and the issue of Frauds and misconduct.
If any one interested to participate in the program information available on www.cliniminds.com or candidates can directly mail info@cliniminds.com to get the prospectus and registration form. Cliniminds also conducted customized workshops to corporate companies like Biocon, Merk , Max and organizations like NIH and proven the excellence in the same. If any requirement for in-house customized training solution for the corporate, contact Mr.Kamal Shahani at 09311168241.
