Delsie Braganza

Delsie joined the Focal Point Research team in 2011 and has been an invaluable asset for our clients. With her strong regulatory and quality assurance background, she is able to help clients understand the Canadian and US requirements, set targets to achieve compliance, and attain their goals to get products to market.

Delsie is able to audit facilities, set up and maintain GMP compliant facilities, develop strong quality management systems, and co-ordinate successful Health Canada inspections. In addition to this, Delsie oversees all regulatory compliance reviews and submissions made to Health Canada and the US FDA.

Delsie obtained an Honours Bachelor of Science (Hons. B. Sc.) in Pharmaceutical Chemistry from the University of Toronto, Post-Graduate Certificate in Pharmaceutical Regulatory Affairs and Quality Operations (RAQ) from Seneca College and Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professional Society (RAPS).

When she’s not learning something new, Delsie loves spending time with family, going on road trips or long walks, and swimming.

Articles

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Reminders

Jun 13, 2022

Reminder for DIN Renewals As a DIN Owner, you should have received your Annual DIN Renewal package from Health Canada. These are due to be submitted by July 29, 2022. Should you require assistance with this, please reach out. FDA User Fees For OTC Monograph Drug...

California Assembly Bill No. 818

Apr 14, 2022

If your company sells or intends to sell disposable wipes in the State of California, this bill will be important to you. The bill was signed on October 06, 2021 and requires premoistened nonwoven disposable wipes manufactured on or after July 1, 2022, to be labelled...

New Legislation for North Carolina

Apr 14, 2022

A new act - HB 528 - will require cosmetic manufacturers to disclose on their website the full list of ingredients, including component ingredients within fragrances, flavours and colour additives. In addition, manufacturers would be required to disclose the CAS...

Amendment to the Quebec Charter of the French Language

Apr 14, 2022

When it comes to trademarks, there is currently an exemption for French-language requirements for owners of “recognized trademarks” who may display a trademark in a language other than French as long as the trademark is legally recognized as a trademark and there is...

Potential Presence of Toxic Substances in Cosmetics

Apr 14, 2022

If you are a manufacturer, distributor, importer, or consumer of Cosmetics in Canada, please read the following information for the safety of the environment and human health: Certain cosmetics contain chemicals called per- and polyfluoroalkyl substances (PFAS). The...

FDA OTC MONOGRAPH DRUG USER FEE RATES FOR FISCAL YEAR 2022

Mar 17, 2022

On March 14, 2022, the U.S Food and Drug Administration (FDA) has announced the rates for over the counter (OTC) monograph drug user fees for fiscal year (FY) 2022 in a Federal Register Notice (FRN) titled ‘Over-The-Counter Monograph Drug User Fee Rates for FY 2022”....

NOTICE WITH RESPECT TO CERTAIN SUBSTANCES ON THE REVISED IN COMMERCE LIST (R-ICL)

Mar 17, 2022

The Department of the Environment published a notice on March 12, 2022 to collect information on the commercial status and use of approximately 700 substances including biopolymers, plant extracts, mineral extracts, proteins, fats, animal extracts, waxes and...

Full Producer Responsibility for Post Consumer Waste in Ontario

Oct 26, 2021

Ontario is moving its existing waste diversion programs to a producer responsibility model. Producers are the companies that design, create and market products and packaging. Producers will be responsible for managing and paying for the full life-cycle of their...

FDA Withdrawal of Temporary Guidances for Alcohol-Based Hand Sanitizers

Oct 26, 2021

Did your company manufacture alcohol-based hand sanitizer or manufacture alcohol for use in hand sanitizers during the COVID-19 pandemic based on temporary policies outlined in FDA guidances originally issued in March 2020? If so, it is important for your company to...

Jan. 01, 2022 – An Important Date for Cosmetics Sold in California

Jul 13, 2021

The Cosmetic Fragrance and Flavor Ingredient Right to Know Act of 2020 (CFFIRKA) will be in effect starting Jan. 01, 2022. There are a total of 23 designated lists that contain ingredients of concern. If any of these designated lists are updated, companies will have 6...

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The Focal Point Research team is ready to help with all of your scientific and regulatory needs. Our team has the experience and expertise you need to see your product to market and we are eager to help you.

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Delsie Braganza

Jennifer Porter, BA Psychology, MBA – President & CEO

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If you would like to be added to our newsletter, please send an email to mail@focalpointresearch.net with the subject line ‘Receive FPR Newsletter’.

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