The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements – December 10-14, 2018 in Arlington, VA
The regulatory world for quality management systems (QMS) is changing fast. To succeed in today's global market, the manufacturers of medical devices must understand those requirements. This intensive 4 ½ day course provides quality system [...]
The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements – December 3-7, 2018 in Manchester, UK
The regulatory world for quality management systems (QMS) is changing fast. To succeed in today's global market, the manufacturers of medical devices must understand those requirements. This intensive 4 ½ day course provides quality system [...]
Webinar – Final Guidance for Industry: Use of Electronic Health Record Data in Clinical Investigations – December 6, 2018, 1:00 pm to 2:00 pm
The Food and Drug Administration, Center for Drug Evaluation and Research and Small Business and Industry Assistance (CDER SBIA), is pleased to announce this virtual event. Issuing the guidance for industry on the use of [...]
6th International Conference on Stem Cell Engineering 2018 – December 5-7, 2018 in Los Angeles, CA
Presented by the Society for Biological Engineering (SBE), this conference will bring together leaders and trainees from cutting edge fields of stem cell engineering including basic and applied studies to discuss progress and needs to [...]