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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.

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Jennifer Porter, BA Psychology, MBA – President & CEO

​Having started at Focal Point Research in 2011, Jenn has been fully engaged in the company and since day one, has leveraged her MBA and interest in the regulated products industries to grow her passion for the business and services offered. 

Jenn has excelled at building on initial conversations with a variety of companies from all industries seeking regulatory and quality assurance services. She has developed strong relationships with each client, offering each one a unique opportunity to have the Focal Point Research team help them develop successful strategies and bring products to market, while ensuring their compliance needs are being fulfilled. 

Jenn has not only been a leader internally, but a key contact for all clients and in 2021, Jenn was the obvious choice to lead Focal Point Research into the future as the successor to company founder, Rob Fichtner.

Jennifer balances her career by honouring her wanderlust, spending her leisure time golfing, and enjoying the outdoors with her loving dog.

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Robert Fichtner

Since co-founding Focal Point over 20 years ago, Rob has led our Regulatory and Scientific practice. A chemist by training, his experience includes Cosmetics, Drugs, Medical Devices, Consumer Products and Natural Health Products (Dietary Supplements). Rob has participated in the launch of thousands of products including their formulation, manufacturing and regulatory submissions for approval. His wealth of experience spans almost 40 years in innovation.
Rob has been involved in all aspects of innovation and new product development. He shares some of his insights in his new video series “Lectures in Innovation”. You can view the first video here.
When not supporting innovators, Rob spends his time becoming a better sailor and guitar player.

(905) 271 2709 mail@focalpointresearch.net
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U.S.-China Tariff Increase Updates

by Jenn Porter | May 21, 2019 | Canadian Regulatory, Cosmetics, Medical Devices, Research/Science/Technology, U.S. Regulatory

The Office of the United States Trade Representative (USTR) formally published a notice in the Federal Register on May 10th of an increase in tariffs from 10% to 25% on all List 3 products being imported from China. The 10% Tariff remains in effect until June 1st for...

Effects of Sterigenics Plant Shutdown on Medical Device Licences (MDL) in Canada

by Jenn Porter | May 1, 2019 | Canadian Regulatory, Medical Devices, Research/Science/Technology, U.S. Regulatory

Sterigenics, an international company who provides sterilization solutions for medical devices, pharmaceutical, commercial, and food industries, has shut down its plant in Willowbrook, Illinois. The recent shutdown, which took place in February 2019, was linked to the...

Wearable Artificial Kidney (WAK) – A Portable Dialysis Device

by Jenn Porter | Apr 3, 2019 | Medical Devices, U.S. Regulatory

Most dialysis patients are presented with limited options for having a great quality of life. The quality diminishes further when they must consume 20-30 pills a day and have to put a harsh cap on their amount of fluid intake. Due to kidney dysfunction, they are in...

Reclassification of High-Level Disinfectants and Sterilant Solutions as Class II Medical Devices

by Jenn Porter | Mar 26, 2019 | Canadian Regulatory, Medical Devices

Health Canada issued a notice on March 18th, 2018 regarding changes to classification of high-level disinfectant and sterilant solutions intended for use on medical devices. Instead of being regulated by the Food and Drug Regulations (FDR), disinfectants and...

Alexa – Your New Best Friend for Cardiovascular Health?

by Jenn Porter | Mar 5, 2019 | Medical Devices, Research/Science/Technology

For patients facing the ongoing health concern of having high blood-pressure, it can be difficult to monitor the status of their condition over a long period of time. It may be a feasible option to check blood-pressure on a daily basis, and take medication to control...

An Apple a Day Keeps the Doctor Away: Apple Watch and the Monitoring of Disease and Disorder

by Jenn Porter | Jan 23, 2019 | Medical Devices, Research/Science/Technology, U.S. Regulatory

There’s no denying that Apple has made great strides in the areas of technology, leaving consumers clamoring at the doors of just about every store whenever a new release is made. The pinnacle of innovation, their sleek designs intricately coalesce with a complex...
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