Rachelle D’Souza, CEO of Regulatory Heights Inc., has successfully licensed various medical and consumer products and facilities with international regulatory authorities / agencies for multinational and start-up 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 numerous articles on the latest international regulatory developments have been published in print and on-line by regulatory professional associations 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.

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Rachelle D’Souza

07
Wed
Jun, 2017

Speaker: Rachelle D’Souza
Duration: 60 Minutes
Product ID: 700723

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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 printing medical devices.more...

Rachelle D’Souza

05
Wed
Jul, 2017

Speaker: Rachelle D’Souza
Duration: 60 Minutes
Product ID: 700744

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Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations

If you are a sponsor of a clinical trial involving a drug, biologic, medical device or combination product, a clinical investigator, a contract research organization (CRO) or an institutional reviemore...

Rachelle Rachelle

Speaker: Rachelle D’Souza
Duration: 60 Minutes
Product ID: 700715

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Cosmetic Testing for US FDA Compliance

The US Food and Drug Administration (FDA) hold cosmetic manufacturers and distributors responsible for the safety and quality of their cosmetics. This webinar serves to guide cosmetic manufacturers more...