PPT-Regulatory review and assessment

Regulatory Control Training Workshop Regulatory Cooperation Forum Luis Lederman 610 November 2017 Morocco Learning Objectives After going through this presentation the participants are expected to be familiar with. National Tribal Forum. Tulsa, Oklahoma. May 2012. . Overview. NAAQS updates . NAAQS process. Particulate matter status. Ozone status. Ozone designations. SO2 NAAQS implementation – discussion. Other notable regulations. . PC – Small Business Development . 7. th. February 2017. Why?. To Radically Reform the . Regulatory Environment. Radical Regulatory Reform. Consequences. Kickstart the SMME . Revolution. . Ease entry into the mainstream . 101:. Your 1. st. Product . Launch . in. Canada. , Europe and the USA. What’s Your Goal?. ISO 13485 Certification. Canadian Medical Device Licensing. CE Marking for Europe. FDA 510(k) Clearance. Sales. Development for Safety of Nuclear Installations. RCF Plenary Meeting. 30 September 2016. Vienna, Austria. Greg . RZENTKOWSKI, Director. Division of Nuclear Installation . Safety. Nuclear Safety and Security Department . Update on the WHO NRA Global Benchmarking Tool. HIS/EMP/RHT/RSS. Outline. Between the 1. st. and the 2. nd. International Consultations. Discussions of the 2. nd. International Consultation. Outcomes and next . Anne E. Loccisano, PhD, DABT. Exponent, . Inc. VP-Elect, SOT/RSESS. GSLC-RSESS Webinar. October 31, 2017. What do regulatory toxicologists do anyway?. Broadly, regulatory toxicologists and risk assessors provide science-based advice to. Update on the WHO NRA Global Benchmarking Tool. HIS/EMP/RHT/RSS. Outline. Between the 1. st. and the 2. nd. International Consultations. Discussions of the 2. nd. International Consultation. Outcomes and next . Anne E. Loccisano, PhD, DABT. Exponent, . Inc. VP-Elect, SOT/RSESS. GSLC-RSESS Webinar. October 31, 2017. What do regulatory toxicologists do anyway?. Broadly, regulatory toxicologists and risk assessors provide science-based advice to. Update on the WHO NRA Global Benchmarking Tool. HIS/EMP/RHT/RSS. Outline. Between the 1. st. and the 2. nd. International Consultations. Discussions of the 2. nd. International Consultation. Outcomes and next . The United States PerspectiveDisclaimer This talk represents my personal views and is not a reflection or a statement of OMB policy or positionsNancy Beck PhD DABTOffice of Information and Regulatory 1Coherence Cooperationin theTransatlantic Trade and Investment Partnership TTIPThe US Chamber of Commercebelieves that five regulatory components are essential to achieve a comprehensive and ambitiou to request assistance Our Office of Information Management and Technology OIMT will work with your firm to set up secure communicationsPlease notify the investigator of any delays due to this encrypti Phase 2 Human Health Risk Assessment of Oil and Gas Activity in Northeastern British Columbia. 1. Presentation outline. Introduction to the study. Key findings. Recommendations. Next steps. 2. Goals. Kent Shigetomi. Office of the U.S. Trade Representative. Overview. What is Good Regulatory Practice?. Why is GRP important?. What are the elements of GRP?. How do you evaluate or measure GRP?. GRP in Trade Agreements.