Chemie.DE Events

XGen Congress

Fri, 02 Oct 2009 15:09:16 GMT

15 Mar 2010 - 19 Mar 2011��San Diego, CA, USA��Welcome to the Decade of the Genomics Revolution! Technological advances are now enabling faster and cheaper mapping of DNA/RNA allowing genomic comparisons and accelerating genomic discoveries. Cambridge Healthtech Institute is proud to launch The ...

CTD Dossier Requirements Focus on EU Module 1 and Quality Module 3

Fri, 19 Feb 2010 16:55:58 GMT

21 Mar 2010 - 22 Mar 2010��Mumbia, India��Techniques to Ensure High Quality Registration Dossiers Facilitate the Registration Procedure for Generics. This Module provides a comprehensive description on the Common Technical Dossier structure � completely updated to reflect the latest changes ...

Non-Interventional Studies in Europe

Wed, 30 Dec 2009 09:19:08 GMT

22 Mar 2010��K�ln, Germany��Non-interventional studies (NIS) are efficient instruments to come to comprehensive conclusions regarding the application as well as the efficacy of pharmaceuticals by means of a representative group of patients. But conducting multinational NIS is ...

How to comply with recent expectations for Extractables /Leachables testing for Biologics

Fri, 19 Mar 2010 12:14:54 GMT

22 Mar 2010��Palo Alto, USA��This Webinar will discuss the test conditions of Extractables/Leachables and also the requirements for testing extractables/Leachables. Areas Covered in the Seminar: Regulatory requirements for testing extractables/Leachables. Test conditions for ...

Overview of FDA Regulatory Compliance for Medical Devices

Thu, 05 Nov 2009 16:16:17 GMT

22 Mar 2010 - 23 Mar 2010��Dublin, Ireland��This course is specifically focused on the law, regulations and policies set down by the FDA for the manufacture of medical devices. It will provide each attendee with the background and knowledge necessary to understand the organization, structure ...

DIA/FDA CDER/CBER Computational Science Annual Meeting

Fri, 19 Feb 2010 16:59:48 GMT

22 Mar 2010 - 23 Mar 2010��North Bethesda, USA��Call for Poster Abstracts extended to March 1, 2010 FDA Forum to Promote Progress in Computational Science from Regulatory and Product Development Perspectives One of the most important and unrecognized issues contributing to drug development and ...

Understanding Polymorphism & Crystallisation

Thu, 09 Jul 2009 14:53:22 GMT

22 Mar 2010 - 24 Mar 2010��Nice, France��This course teaches chemists and engineers some fundamental aspects of crystal chemistry, nucleation and crystal growth, the operation of batch crystallisers and methodologies of characterisation. Salt selection and polymorph control and selection ...

microRNA in Human Disease & Development

Fri, 02 Oct 2009 15:11:52 GMT

22 Mar 2010 - 24 Mar 2010��Cambridge, MA, USA��The role of microRNA in regulating mammalian development and disease is now well established. miRNAs represent a novel class of targets for therapeutic and diagnostic development, currently not fully exploited by the pharmaceutical and biotechnology ...

Nigeria's Oil & Gas Legal System

Wed, 18 Nov 2009 16:55:08 GMT

22 Mar 2010 - 26 Mar 2010��LAGOS, Nigeria��This course will provide you with a comprehensive overview of the legal and fiscal systems that govern Nigeria's oil and gas industry with references to crucial lessons learned around the world. You will address issues in the current system and look ...

Nigeria's Oil & Gas Legal System

Wed, 18 Nov 2009 17:02:32 GMT

22 Mar 2010 - 26 Mar 2010��LAGOS, Nigeria��Nigeria's Oil & Gas Legal System Course Overview This course will provide you with a comprehensive overview of the legal and fiscal systems that govern Nigeria's oil and gas industry with references to crucial lessons learned around the world. You ...

World Fiscal Systems for Oil & Gas

Mon, 23 Nov 2009 10:44:03 GMT

22 Mar 2010 - 26 Mar 2010��SINGAPORE, Singapore��World Fiscal Systems for Oil and Gas is a 5 day computer-based interactive training course. It is based on a work book with examples and exercises. Participants will receive, free of charge, the petroleum fiscal software used during the course. This ...

Biotechnology for Non-Biotechnologists

Mon, 18 Jan 2010 11:06:46 GMT

23 Mar 2010 - 24 Mar 2010��Barcelona, Spain��Objectives This course will provide Non-Biotechnologists with an overview and insight in pharmaceutical biotechnology. It will also present the opportunities of biotechnology in GMP manufacturing. Common aspects of production analytics will be ...

CTD, CEP and Active Substance Master File

Mon, 18 Jan 2010 11:09:27 GMT

23 Mar 2010 - 24 Mar 2010��M�nchen, Germany��Objectives This education course is intended to provide guidance on the format, content and submission procedures for the pharmaceutical documentation of the quality of the drug substance for different types of dossiers, the CTD, the CEP and the ...

Evidence-based Medicine & Health Technology Assessment: Moving From Separate Appraisals to Synergistic Communications

Fri, 19 Feb 2010 17:05:58 GMT

23 Mar 2010 - 24 Mar 2010��Washington DC, USA��Learn how the once distinct roles involved in developing guidance for evidence-based medicine (EBM) and health technology assessment (HTA) are coming together, particularly from a communications and dissemination perspective.

3rd Oligonucleotides-based Therapeutics Conference

Fri, 19 Feb 2010 17:03:20 GMT

23 Mar 2010 - 25 Mar 2010��Bethesda, USA��FEATURED TOPICS � Non-Clinical � Chemistry, Manufacturing, and Controls (CMC) � Clinical Development � Oligonucleotide Safety Working Group Updates Featured Keynote Speakers: Mauro Ferrari, PhD, Professor and Chairman, Department of Nanomedicine ...

analytica 2010 - 22nd International Trade Fair for Laboratory Technology, Analysis and Biotechnology

Thu, 26 Nov 2009 13:25:42 GMT

23 Mar 2010 - 26 Mar 2010��M�nchen, Germany��analytica 2010 will present products and innovations in the analysis, laboratory- technology and biotechnology sectors with the usual high level of quality. As always, several manufacturers will use this attractive platform to introduce new products ...

CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3

Fri, 19 Feb 2010 17:09:04 GMT

24 Mar 2010 - 25 Mar 2010��Hyderabad, India��Techniques to Ensure High Quality Registration Dossiers Facilitate the Registration Procedure for Generics. This Module provides a comprehensive description on the Common Technical Dossier structure � completely updated to reflect the latest changes ...

Root Cause Analysis for CAPA

Thu, 05 Nov 2009 16:18:02 GMT

24 Mar 2010 - 26 Mar 2010��Dublin, Ireland��Upon completion of this course, participants will have gained an understanding of the basic concepts involved in Root Cause Analysis and the tools used to conduct this activity. Participants will learn through experiential activities such as group ...

FDA Guidance on Adaptive Design for Clinical Trials

Fri, 19 Feb 2010 17:11:49 GMT

26 Mar 2010��Silver Spring, USA��Build a Solid Foundation in the Regulatory Aspects of Adaptive Designs. There has been increasing interest in applying adaptive clinical trials throughout the various stages of clinical development. This conference will provide an overview of the ...

Calibration and Qualification in Analytical Laboratories

Fri, 19 Mar 2010 12:34:42 GMT

26 Mar 2010��Palo Alto, USA��A detailed understanding of calibration and qualification of lab equipments, development of qualification master plan, allocation of equipments to qualification categories A, B, C, the approach for existing system qualification. Areas Covered in the ...