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One of the owners of (845) 634-6406 is between 60-70 years old. We have records for 3 possible previous addresses for the owner, 6 other possible phone numbers, and 2 possible related persons connected to this individual.
Activities and Societies: Tst102 Sys101 Stm202 Pqm101 Clm031 Clm017 Clm014 Cle068 Cle045 Cle023 Cle035 Cle025 Cle021 Cle004 Cle003 Cle001 Clb016 Clb007 Acq201a Acq101 Con121 Con124 Con127 Clm013 Clm016 Clc106 Clc222 Clm024 Clb011 Clm003 Cle026 Clc036 Irm101 Cle009 Cll008 Cle022 Clv017 Cle301 Evm101 Cle012 Cle015 Clm021 Clm035 Clm012 Clv018 Clv020 Clc011 Cll011 Stm303 Cli001 Cli002 Cli003 Sys202 Cle006 Cmq100 Cle008 Clb034 Clm055 Clc008 Clb024 Clb026 Clc047 Clm056 Clc060 Cle017 Con100 Clc131 Clb029 Clc063 Clb030 as of July 2015, Seventy One Courses were Completed. These Completed the Course Requirements for Level 3 Stm, Level 1 Pm, Level 1 Engineering, Level 1 Contracting, and Level 1 Finance. Additional Coursework for Contracting Officer Representative (Cor) was Also Completed. Two In-Person Classes (Stm 202 and Stm 303) were Completed.Note That the Term &Quot;Qualified&Quot; is Used, Since to be &Quot;Certified&Quot; would Require Being A Federal Employee. i was Able to Take This Training on MY Own Time Since MY Position at Engility Supported the Dod. i Strongly Believe This Effort was Essential for Being Able to Bridge Between Pharmaceutical and Dod Research Philosophies, Setting the Stage for A Business Process Re-Engineering Effort of the Dod'S Early Drug Discovery Research to Align with Fda Regulatory Requirements for Drugs, Biologics and Medical Devices. Show Less
Activities and Societies: Regulatory Affairs Certification (Rac) Passed in April 2016 Certificate Classes Included:-Ethics-Global Regulatory Strategy for Medical Devices-Global Regulatory Strategy for Pharmaceuticals-Medical Devices: Definition and Lifecycle-Pharmaceuticals: Definition and Lifecycles-Role of the Regulatory Professional-Regulation of Generic Drugs in the Us-Regulation of Combination Products-Regulation of US and EU Biologics-Good Laboratory Practices (Glps)-Good Manufacturing Practice (Gmp)-Regulatory Due Diligence for Product Development-Chemistry, Manufacturing and Controls-Pharmaceuticals: US Regulations Show Less
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