Meet the Team
Meet Some of the Global 80+ Professionals that Make LS Law Possible
Teenah C
Regulatory & Quality Consultant
Overview of Experience
I am an innovative and successful Quality Assurance manager with over 14 years of experience in various sectors, including Medical Cannabis, Medicines, Food supplements, Cosmetics, Household, and Medical devices. I have a proven track record for bridging the gap between commercial objectives and compliance.
With strong commercial skills gained throughout the years, I am also very experienced in developing new business opportunities and compliance strategies. I thrive in dynamic environments and adapt to the ever-changing demands of the legal and compliance aspects of the industry.
I have worked in a number of life science organisations before joining Life Science Law as a Quality Assurance Consultant, including Reckitt Benckiser, Medisonal, the Novisom Group and the British Indpendant Pharmacy Whoelsale Association (BIPWA).
Areas of Expertise
Good Distribution Practice (GDP).
Good Manufacturing Practice (GMP).
Good Clinical Practice (GCP).
Pharma Quality Assurance.
Responsible Person Officer.
Contract drafting and negotiation.
Audit and Monitoring.
Data Entry.
SOP development and training.
Regulatory Bodies of Expertise
MHRA,
EMA,
ABPI.
Track Record
In my role as Head of Quality Assurance & Regulatory Affairs at Medisonal, I played a crucial role in supporting the launch of a start-up specializing in Medical Cannabis and cannabinoids. I provided expertise to the management team on quality compliance requirements, successfully pitched to potential investors, and managed the quality compliance aspects of the business. I also contributed to organizing charity events in collaboration with patient groups and headed PR and marketing efforts tailored to the industry’s unique needs.
During my tenure as the Commercial Quality Manager UK & Ireland at Reckitt Benckiser, I oversaw the quality and compliance of all health products, including medical devices, cosmetics, and household items. I took on the role of Responsible Person duties for the UK and Ireland, led GMP and GDP quality improvements, conducted audits, and managed issue resolution, ensuring that quality objectives aligned with commercial needs.