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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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The Future is Now: A Zero Contact Ultrasound

The Future is Now: A Zero Contact Ultrasound

by Jenn Porter | Feb 15, 2020 | Canadian Regulatory, Cosmetics, European Regulatory, Innovation, Medical Devices, Natural Health Products, Our View, Research/Science/Technology

Just over one week into the new decade and the medical device industry is already launching into the future. The innovative researchers at Massachusetts Institute of Technology (MIT) have taken a large step into the future of ultrasound imaging technologies. They have...
Health Canada Announces the Creation of a New Medical Devices Directorate

Health Canada Announces the Creation of a New Medical Devices Directorate

by Jenn Porter | Dec 18, 2019 | Canadian Regulatory, Medical Devices, Research/Science/Technology, Uncategorized

Health Canada has announced the creation of a new Medical Devices Directorate (MDD). This was done in order to account for and accurately reflect the current medical device industry, which has evolved drastically over the past several years. The new Directorate will...
Feeling Blue: Can Blue Light Damage Your Skin?

Feeling Blue: Can Blue Light Damage Your Skin?

by Jenn Porter | Oct 22, 2019 | Canadian Regulatory, Cosmetics, Medical Devices, Natural Health Products, Research/Science/Technology, U.S. Regulatory

While the general public is largely aware of the harmful effects ultraviolet (UV) light can have on our bodies, as well as the basic measures that should be taken to protect ourselves against such effects, the dangers surrounding blue light seem to go relatively left...
Can Health Features on Devices Detect Dementia Signs?

Can Health Features on Devices Detect Dementia Signs?

by Jenn Porter | Aug 21, 2019 | Canadian Regulatory, Medical Devices, U.S. Regulatory

Apple Inc. and pharmaceutical giant Eli Lilly have joined forces to conduct research on whether dementia and signs of cognitive decline can be detected via health features on the iPhone and Apple Watch. Evidation, a health tech startup, is also involved in the...

Sterigenics Makes Deal to Reopen Willowbrook Sterilization Plant

by Jenn Porter | Jul 30, 2019 | Events/Company Updates, Medical Devices, Research/Science/Technology, U.S. Regulatory

Following the shutdown of an Illinois Sterigenics plant in February of 2019, a deal has been made for it to be reopened, pending approval from the DuPage County Circuit Court. According to a Medtech Dive post, the closure of the Willowbrook plant caused losses of...

European Chemicals Agency (ECHA) Restricts Microplastics and Siloxanes

by Jenn Porter | Jul 9, 2019 | Cosmetics, European Regulatory, Medical Devices, Research/Science/Technology

Intentionally Added Microplastics: Microplastics are manufactured and used in many products on the European market. These ‘intentional’ uses of microplastics are the focus of the proposed restrictions. The potential posed environmental and human health risks of...
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