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DTSTART:19700308T020000
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UID:2140535:Event:64629
DTSTAMP:20260525T225456Z
SUMMARY:Webinar On Risk Management and Risk Analysis Techniques in Cli
 nical Trials
DESCRIPTION:If you are currently involved in clinical trials either as
  a CRA, project manager, investigator or sponsor, this seminar will pr
 ovide you with an overview of risk factors in clinical trials and poss
 ible ways to mitigate, control, assess impact, and prevent them in you
 r trial. We would discuss the key elements of risk management such as 
 planning, identification, quantification, action, measurement, outcome
  assessment, and post-implementation review of various types of risks.
  Also discussed will be best practices for risk analysis and prospecti
 ve planning in the project plan. At the end of the seminar, you would 
 be able to review your current project plan for potential issues or he
 lp address these factors in the future clinical trial project plans th
 at you may create.  If you are aspiring to be a clinical project mana
 ger, are sponsoring a clinical trial, supervise clinical trial operati
 ons, or would like to become a clinical site, this course is a must fo
 r you.\nManaging clinical trials is arguably one of the most difficult
  jobs in the medical product development industry. Clinical trials are
  highly complex projects with numerous unpredictable factors that coul
 d influence their successful outcome. Several events could adversely a
 ffect a clinical trial outcome such as not being able to recruit subje
 cts in a timely manner, managing difficult sites, trial supply issues,
  biological sample handling, regulatory trouble-shooting, and many mor
 e. A key component of clinical project management is the ability to id
 entify potential risks and implementing measures to manage them. This 
 seminar will provide the basics of clinical trial risk management and 
 analysis techniques and practical tips to clinical trial professionals
  and sponsors using case studies from the presenter’s experiences.\n
 Areas Covered in the Session :\nCommon risk factors in clinical trials
 \nRetrospective and prospective risk analysis techniques\nRisk managem
 ent: Key techniques in risk reduction, assessment, addressing, trainin
 g and communication\nRisk analysis plan: identification, information g
 athering, decision, implementation and review\nRoles and responsibilit
 ies of various personnel in risk reduction\nOverview of FDA requiremen
 ts for risk management                     \nExpe
 ctations and responsibilities of the clinical project manager\nRole of
  various clinical team members: CRA, coordinators, sponsors and invest
 igators\nChallenges of large-scale and international clinical trials\n
 Do’s and Don’ts for risk management of a clinical trial\nWho Will 
 Benefit:\nClinical Project Managers\nClinical research associates\nCli
 nical coordinators\nPrincipal Investigators and sub investigators\nIRB
  personnel\nRegulatory Vice Presidents, Directors and Managers at spon
 sors\nAttorneys – In-house or Outside Counsel\nPrice tags:\nLive\nSi
 ngle Live : For One Participant\n$ 249\nCorporate Live : For Max. 10 P
 articipants\n$ 899\nRecording\nSingle REC : For One Participant - Unli
 mited Access for 6 Months\n$ 299\n\nFor more information visit https:/
 /medtechiq.ning.com/events/webinar-on-risk-management-and-risk-analysi
 s-techniques-in
DTSTART;TZID=America/New_York:20140908T130000
DTEND;TZID=America/New_York:20140908T143000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1310
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1310
CONTACT:4169154458
ORGANIZER;CN=compliancetrainings:https://medtechiq.ning.com/profile/co
 mpliancetrainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
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