General Counsel and Chief Compliance Officer

• Jan 2023 - Present

General Counsel

• Jan 2020 - Dec 2022

Of Counsel

• Dec 2016 - Jan 2020

Draft and negotiate SaaS Agreements, Distribution Agreements, Employment and Contractual Work Agreements Provide legal support to Business, Marketing and Sales UnitParticipate in sales conference, main point of contact to various business units to address legal issues

General Counsel and Chief Strategist

• Jun 2018 - Jan 2020

I work with extremely talented, experienced and solutions driven Elocity Management, Advisory and Product Development Team, to deliver cutting edge solutions which will revolutionize the electric mobility industry. We work at the cross roads of IoT, blockchain, data science and analytics to produce sustainable cleantech solutions. I work with extremely talented, experienced and solutions driven Elocity Management, Advisory and Product Development Team, to deliver cutting edge solutions which will revolutionize the electric mobility industry. We work at the cross roads of IoT, blockchain, data science and analytics to produce sustainable cleantech solutions.

Lawyer

• Jun 2017 - Jan 2020

Civil litigation Contractual disputes Intellectual property litigation (trademarks, copyrights and patents) Technology law, Privacy and Data Protection Laws Healthcare laws (Canada, US and EU) Civil litigation Contractual disputes Intellectual property litigation (trademarks, copyrights and patents) Technology law, Privacy and Data Protection Laws Healthcare laws (Canada, US and EU)

Associate Lawyer

• Jun 2016 - Sep 2016

d■ Advise corporate clients on regulatory matters pertaining to food and drugs act and regulations, privacy and data protection legislation, Ontario's accessibility legislation compliance, advertising and marketing law, competition law, laws governing Ontario's regulated health professions, Patent Act and Regulations, Trademarks Act and Copyrights Act■ Conduct freedom to operate due diligence for pharmaceutical patents, and draft legal opinions for pharmaceutical, biotechnology, technology and consumer products clients' in the US, European Union and Canada■ Prepare and maintain clients' corporate files, draft officers and directors resolutions, draft and revise shareholder agreements■ Review and revise master services agreements, statements of work, conduct scope analysis for change of work orders for firm's large corporate clients ■ Advise major client on the website accessibility compliance requirements under the Ontario's disability legislation (AODA); prepare position summary to facilitate successful negotiation of an impending change order Show less

Student at Law

• Aug 2015 - Jun 2016

I worked on a broad range of corporate commercial, intellectual property and regulatory matters for various corporate clients. Some of my representative work included: ■ Assisted in drafting and provided negotiation support for a broad range of agreements such as service and supply agreements, distribution agreements, sales and purchasing agreements, consultant agreements, license agreements, confidentiality agreements, and clinical trial agreements;■ provided legal advice on a wide range of regulatory matters, including, but not limited to Health Canada and FDA marketing, (advertising, promotion, labelling) Canada's anti-spam legislation, (CASL); internet/digital, social media and e-commerce issues■ drafted agreements for technology-related goods and services, including SaaS, telecom, consulting, software licensing and hardware purchase agreements, statements of work, change orders, amendments and non-disclosure agreements (NDAs)■ Assisted patent litigation group with legal research, expert witness cross examination preparation, drafting memorandum of fact and law, prepared compendiums, and document management■ Assisted in the drafting of regulatory submissions for generic market entries Show less

Legal Intern, Counsel - Xpert Credit Control Solutions Inc.

• Jan 2013 - Sep 2016

■ Draft, revise, review and negotiate sale & purchase agreements, commercial lease agreements and amendments to the commercial lease agreements ■ Draft pleadings and Attend Ontario Municipal Board (OMB) hearings related to municipal by-law amendment related matters ■ Draft disposition requests and related closing documents ■ Review applicable searches in preparation of conveyance of a clear title ■ Draft statement of claims to initiate power of sale remedies under the Mortgages Act ■ Attend discoveries, motions and assist senior litigation counsel in preparation of default mortgage actions Show less

Legal Intern- Intellectual Property and Government Affairs

• Sep 2014 - Dec 2014

As a member of the Government Affairs department I provided assistance and support to the Director of Government Affairs such as: ■ monitored pharma industry related regulatory and legal developments; ■ participated in the the Pharmaceutical Research and Manufacturers of America (PhRMA) and advisory meetings ■ appraised Canada’s pharmaceutical industry related intellectual property laws and compared with the laws in United States of America, United Kingdom, Germany, France, Japan and Singapore Show less

Summer Student

• May 2013 - Aug 2014

Civil litigation Medical Malpractice and Personal Injury (Plainttiff side) Pharmaceutical and Medical Device Class Actions Civil litigation Medical Malpractice and Personal Injury (Plainttiff side) Pharmaceutical and Medical Device Class Actions

Counsel (Probono)

• Sep 2013 - Apr 2014

Represented clients at the Health Professions Appeal Review Board (HPARB) hearing Represented clients at the Health Professions Appeal Review Board (HPARB) hearing

Clinical/Medical Researcher (medical devices and pharmaceuticals)

• 2008 - 2012

I was a part of the Arrhythmia Services, Cardiology Unit of the Sunnybrook Health Sciences, and was responsible to manage all aspects of several global and Canadian pharmaceutical and medical device related randomized controlled trials. During my 4.5 years with Sunnybrook, I interacted and worked with a broad base of stakeholders related to the pharmaceutical and medical device/ health care industry such as, health care professionals, drug/ medical devices sales and marketing specialists, in-house and study sponsor legal counsel, regulatory affairs specialists and business development managers. This position gave me first hand experience to address drug and medical devices development and approval related regulatory challenges. As the senior clinical/medical researcher I provided following services to the research department: ■ prepared clinical trial applications (CTAs) and CTA amendments; ■ responded to Health Canada's claxifaxes; ■ prepared clinical study site initiation related documents including clinical study master binders; ■ negotiated Master Trial Agreements (MTAs) on the behalf of the clinical study team; ■ drafted site operating procedures (SOP) manual to ensure site quality assurance and control ■ trained staff and members of the clinical research team; ■ regularly conducted research induction meetings and and presentations; ■ assisted the drug and medical device sponsor teams with regulatory compliance for timely product approval and market access; ■ performed due diligence for Health Canada's audit and assisted study sponsor with FDA site audit; ■ regularly communicated with the local and regional Ethics Board for clinical trial approvals, and to provide routine update on any protocol deficiencies or adverse event occurrences ■ prepared grant proposals for investigator initiated studies; drafted grant reports in accordance with the grant agencies requirements; reviewed financial status of grant accounts; drafted adjustment reports Show less