Live webcast Implementing Best Practices for Global Regulatory Intelligence Programs:Dos and Don'ts
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Website https://compliance2go.com/product/?pid=CP2014-429 |
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Category Biotechnology ;Medical Device ;Pharmaceutical
Deadline: March 24, 2015 | Date: March 25, 2015
Venue/Country: Online, U.S.A
Updated: 2015-03-03 17:12:22 (GMT+9)
Call For Papers - CFP
DESCRIPTIONThis webinar is intended to help you get familiar with the best practices for global regulatory intelligence programs including dos and don’ts. This webinar is further intended to increase our awareness for the importance of implementing a holistic global regulatory intelligence program suitable for your medical product types. It is believed that actionable and practical regulatory intelligence can help an organization save a significant amount of resources (time, efforts and financial). Thus, it is imperative we become aware of and get familiar with the best practices for developing a global regulatory intelligence program. This webinar will address the best practices for you to take action, significantly benefiting your organization in many ways. Why Should you AttendTo adequately develop and implement a holistic global regulatory intelligence program. Areas Covered in the WebinarApplicable Laws and RegulationsGuidance, Rules, and StandardsRegulatory Intelligence for Drugs, Biologics, Biosimilars, and Medical Devices including In Vitro Diagnostic Medical Devices (IVDs)What Is Important to Consider?R&D, Patenting (IP) and Applicable Regulatory PathwaysQuestions and Issues to Identify and AddressTotality and Flexible ApproachesInterfacing: Roles and BenefitsReimbursement Issues: What, When, Why, and HowIntellectual Property (IP) IssuesAlignment between Regulatory Plan/Strategy, Reimbursement, and IPNew Requirements to Integrate: Risk Management Plan (RMP)/Pharmacovigilance (PV)FDA Unique Device Identification/Identifier (UDI)Detailed ContentsCommon Mistakes Leading to Serious Consequences (Patient Safety and Business Operations)Practical, Actionable, and Sustainable Solutions (PASS)Speaker’s Experience and Actual CasesWho will BenefitRegulatory AffairsManagement: CEOs, VPsR&D and Product DevelopmentLegal Counsel and Compliance OfficersMarketingClinical AffairsConsultantsContractors/SubcontractorsOther Interested PartiesWebinar Includes:Q/A Session with the Expert to ask your questionCopy of PowerPoint slides (PDF print only)60 Minutes Live PresentationCertificate of Attendance
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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