Listings tagged with 'fda approval process' (13)

FDA Scrutiny of Promotion and Advertising Practices
FDA Scrutiny of Promotion and Advertising Practices

$150.00

Overview: DTC may be deemed as misbranding your product and, therefore, may not be marketed. Firms must be more sophisticated now in designing their advertis...

15 Preparing Premarket Submissions that secures U.S. FDA ClearancesApprovals 510(k)Pre-IDEIDE and PMA
15 Preparing Premarket Submissions that secures U.S. FDA ClearancesApprovals 510(k)Pre-IDEIDE and PMA

$1,295.00

Overview: This workshop style training course is designed based on 30 year of regulatory affairs experience in preparing more than 150 successful U.S. FDA subm...

Compliance trainings logo
Compliance trainings logo

$229.00

Description : This webinar will provide a comprehensive understanding of the FDA Combination Product system. Participants receive a foundation of knowledge ab...

Compliance Global Inc.
Compliance Global Inc.

$155.00

Overview: FDA investigations can lead to observations requiring remediation, disruption of your business, loss of revenue and enforcement actions up to and i...

3a73bea
3a73bea

$155.00

Overview: The FDA's Design History Files, Device Master Records, Device History Record, and the EU's MDD TF/DD -- Documentation to meet their different purpo...

3a73bea
3a73bea

$155.00

Overview: There is an on-going major shift in the emphasis of Federal Drug Administration cGMP audits. These changes in focus have a major impact on indiv...

3a73bea
3a73bea

$155.00

Overview: FDA Medical Device Recalls are an effective method of removing or correcting consumer devices that are in violation of laws administered by the Foo...

Final
Final

$155.00

Speaker: David R Dills Overview Any Medical Device that is legally in the U.S. may be exported anywhere in the world without prior FDA notification or app...

3a73bea
3a73bea

$155.00

Overview: The Failure Mode Effects Analysis breaks down the analysis of complex software functions into manageable subsystems and modules. It can have a numb...

Compliance Global Inc.
Compliance Global Inc.

$155.00

Overview: The first step in reduced testing is to qualify the supplier using the supplier qualification process. This webinar will review the supplier qualif...

Compliance Global Inc.
Compliance Global Inc.

$155.00

Overview: CAPA (Corrective and Preventative Actions) did not originate in the Pharmaceutical and Medical Device industry or the Automobile Industry as most f...

3a73bea
3a73bea

$155.00

Overview: The purpose of this webinar is to provide the topics and basic instructions needed to establish the quality training systems and related practices ...

3a73bea
3a73bea

$155.00

Overview: Firms exporting products from the U.S. are often asked by foreign customers or foreign governments to supply proof of the products’ status as regul...

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