“PASB was a fantastic group to work with. Helping with implementing our Quality Management Procedures and Policies, Paul & his team were incredibly diligent in their work with a high attention to detail. I would highly recommend PASB for all things regulatory, QA/QC and engineering/product development support.”
Brett Vokey, Founder and CEO, BreatheSuite
“As a medical device distributor, we really enjoy working with Sarah at PASB MedTech Solutions. PASB works hard to provide prompt, efficient service and have helped us tackle many difficult regulatory issues with an open and creative mind. Since FroggaBio began working with PASB we have successfully added a private label medical device to our offerings and obtained approvals to distribute several innovative highly complex medical devices in Canada. We trust them as a partner and would recommend PASB to any medical device distributor or manufacturer who wants to streamline their regulatory operations.”
Moshe Kapelnikov, Managing Director, FroggaBio
“Thanks Sarah and Paul for your tremendous help and diligence especially with the risk and V&V elements. I am 100% sure we would not have been able to close the submission w/o your support.”
Hasnaa Fatehi, Senior Mgr (Regulatory Affairs), I-MED Pharma
“Sarah Bassler at PASB helps with all Medical Device classifications for both US and Canada and is committed to finding the best pathforward for our clients. I have worked with Sarah for the past 3 years and have experienced a truly gifted and knowledgeable Medical Device expert who respondsquickly to questions and is always happy to help. Thank you Sarah for your high level of professionalism and for always being there when I need you.”
Jacqui Jenskey, Director of Regulatory Affairs, Dell Tech Laboratories
“RAR Innovations is a medical technology startup based in St. John's, Newfoundland. We were introduced to PASB MedTech Solutions Inc. through Bounce Health Innovation.
We highly recommend PASB to entrepreneurs and innovators in the medical device industry. Their detailed regulatory assessment gave us a clear understanding of the regulatory requirements for our medical device in Canada and the United States. The templates and in-person training sessions provided by PASB on risk assessment and documentation requirements were incredibly valuable. They allowed us to gain insights that will help us develop medical device innovations well into the future. We are very impressed by the level of detail, guidance and continued support Sarah and Paul provide. We highly recommend PASB to other entrepreneurs and innovators in the medical device industry! Thank you so much for everything!!”
Allie Lynch, Founder, RAR Innovations
