From 29 Jun to 29 Jun 2012, California, Palo Alto This Medical device training will be discussing the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products. Source: Medical Devices: EU Directives, Guidance Documents, CE Marking Process and...

From 25 Jul to 25 Jul 2012, California, Palo Alto This 3-hr Latin America Regulatory compliance requirements training/webinar will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Latin America. Source: Understanding Regulatory Compliance Requirements Across the Life Science...

From 24 Sep to 25 Sep 2012, Germany, Berlin Improving Quality & Compliance and increasing operational excellence with manufacturing execution systems in Pharma & Life Sciences Industries Source: MES & Process Minds 2012 – Pharma & Life Science Industries...

From 1 Dec to 2 Dec 2012, Hong Kong, Hong Kong Prevention is better than cure. This year’s event will deliberately address the prevention strategies against cardiovascular health diseases, with also updates on the various pharmacological advancement in the field of preventive cardiology. Source: 4th Asian Preventive Cardiology and Cardiac Rehabilitation...

From 21 May to 21 May 2012, California, Palo Alto This webinar covers FDA’s expectations from GMP facilities regarding raw material vendor selection,expectations from quality control and documentation processes, and training requirements, with case studies. Source: Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material...

From 18 Jul to 18 Jul 2012, California, San Mateo Leading provider of Oracle’s clinical trial, data, and drug safety software will discuss a major pharmaceutical company’s pharmacovigilance globalization initiative that helped standardize and streamline its operations. Source: Streamlining a Global Life Sciences Company’s Pharmacovigilance...

From 18 Jul to 18 Jul 2012, California, San Mateo Leading provider of Oracle’s clinical trial, data, and drug safety software will discuss a major pharmaceutical company’s pharmacovigilance globalization initiative that helped standardize and streamline its operations. Source: Streamlining a Global Life Sciences Company’s Pharmacovigilance...