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I got it!

Mr David Lim

Researcher

Dr. Lim obtained his Ph.D. in biological sciences at the University of Missouri-Columbia and published his thesis research in the prestigious journal

David spoke at

Webinar on The FDA 510(k) and Q-Submission: Best Practices Compliance Trai... Feb 2016
Webinar On Good Social Media Practices to Avoid FDA Actions Compliance Trai... Jan 2016
Webinar on Complaint Handling & Medical Device Reporting Compliance Trai... Jan 2016
Webinar On Medical Device Laws and Regulations in Asia: China, Hong Ko... Compliance Trai... Dec 2015
Webinar On Good Social Media Practices to Avoid FDA Actions Compliance Trai... Nov 2015
Webinar On Implementing Adequate CAPA and Design Control Procedures Compliance Trai... Oct 2015
Webinar On Establishing an FDA-Compliant UDI System FutureCorp Cons... Oct 2015
FDA 510(k) Requirements, Submission, and Clearance: Best Practices FutureCorp Cons... Sep 2015
Webinar On Preparing for FDA BIMO Inspection and Management FutureCorp Cons... Aug 2015
Webinar On FDA Inspection and Medical Device Design Control FutureCorp Cons... Jul 2015
Webinar On Good Clinical Practices (GCP) FutureCorp Cons... Jun 2015
Webinar On CE Mark: Content and Format for a Technical File and Design... FutureCorp Cons... Jun 2015
Webinar On Quality Risk Management for Drugs and Biologics FutureCorp Cons... May 2015
Webinar On 510(k) Preparation, Submission and Clearance FutureCorp Cons... May 2015
Webinar On Big Data in FDA-Regulated Industry Compliance Trai... Apr 2015
Webinar On FDA Inspection Preparation and Readiness Compliance Trai... Mar 2015
Webinar On Good Documentation Practices for Clinical Trials Compliance Trai... Feb 2015
Webinar On The FDA 510(k) and Q-Submission: Best Practices Compliance Trai... Feb 2015
Webinar On Complaint Handling & Medical Device Reporting (MDR) Compliance Trai... Jan 2015
Webinar On Medical Device Laws and Regulations in Asia: China, Hong Ko... Compliance Trai... Dec 2014
Webinar On Best Practices for 510(k) Drafting and Submission: Dos and ... Compliance Trai... Nov 2014
Webinar on Best Practices for Medical Device Recalls Compliance Trai... Nov 2014
Webinar On Best Practices for 510(k) Drafting and Submission: Dos and ... Compliance Trai... Oct 2014
Best Practices for 510(k) Drafting and Submission Compliance Trai... Oct 2014
Webinar on Current Good Manufacturing Practices (cGMP) for Medical Dev... Compliance Trai... Sep 2014
Webinar on Quality System Regulations (QSRs) for Medical Devices and I... Compliance Trai... Aug 2014
Webinar On Medical Device Reporting Compliance Trai... May 2014
Webinar On - The FDA 510(k): Q-Submission, Preparation and Submission Compliance Trai... Mar 2014
Webinar On - Good Documentation Practices for Clinical Trials Compliance Trai... Feb 2014
Global Medical Device Adverse Event Reporting GlobalComplianc... May 2013
Medical Device Design Control GlobalComplianc... May 2013
FDA-Compliant Medical Device Reporting (MDR) GlobalComplianc... Apr 2013
510(k): Format and Contents GlobalComplianc... Apr 2013
Global Medical Device Adverse GlobalComplianc... Mar 2013
Medical Device Complaint Handling Systems GlobalComplianc... Mar 2013
Current Good Manufacturing Practice GlobalComplianc... Jan 2013
Medical Device Design Control GlobalComplianc... Jan 2013