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Rachelle DSouza

Rachelle D'Souza is Keynote Speaker at ComplianceKey.She is licensed various medical and consumer products and facilities for start-ups and multi-national companies.
Her expertise also includes clinical trial master file documentation, and the design and maintenance of globally compliant quality, safety/pharmacovigilance, and medical information systems.
At Regulatory Heights Inc., Rachelle continuously monitors the current regulatory environment and utilizes regulatory intelligence as a strategic business driver for her clientele. Her articles and webinars on the latest international regulatory developments have been published in print and on-line by regulatory professional associations, webinar hosting platforms and industry magazines around the world.
Her versatility has enabled Regulatory Heights Inc. to support companies, in particular, start-ups with the licensing of their drugs and medical devices in international markets


 Webinar Id: LSHCRD001
 6 months unlimited
 Duration 60 mins
Ratings:
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Use of Electronic Health Record Data (EHR) in FDA-regulated clinical investigations

This webinar will discuss FDA's current recommendations on using electronic health records in prospective clinical investigations of human drugs, biologics, medical devices and combination products.

$167 Recorded (6 months unlimited access)
 Webinar Id: LSHCRD002
 6 months unlimited
 Duration 90 mins
Ratings:
No reviews yet!!

FDA Regulation, 3D Printing and Medical Devices

This webinar on 3D printing will cover FDA's expectations regarding the design, manufacture, testing and approval of 3D printed medical devices.

$167 Recorded (6 months unlimited access)


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