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Sue Place

Regulatory and Quality Manager at Psephos Biomedica

Sue Place is the Regulatory and Quality Manager at Psephos Biomedica, a role she has held for several years. She is a member of the Chartered Quality Institute and brings over 30 years of experience in quality management, particularly within start-up environments. Her expertise encompasses regulatory compliance and quality assurance, which are critical in the biomedical sector.

In her current position at Psephos Biomedica, Sue is responsible for ensuring that the company's products meet regulatory standards and quality benchmarks. This role is vital for maintaining the integrity and safety of biomedical products, which are subject to stringent regulations.

Sue Place's professional background reflects a strong commitment to quality and regulatory affairs, making her a key asset in her field.

Highlights

Dec 31 · linkedin

Are you a Medical device start-up, small business or an experienced business looking for additional help in generating a Quality Management System, transferring to ISO 13485:2016, looking to supply the USA (21 CFR 820) or the new Medical Device Regulation or bringing your European Technical Files up to date? If yes, Psephos Biomedica can help you on a short- or long-term basis. We are based in the South East of England near Brighton and have clients throughout the UK and Europe.
Please get in touch via email [email protected] or phone the office on +44 (0)1273 704527. Psephos Biomedica’s team together have more than 100 years medical device and IVD experience #mdr #iso13485 #Psephos

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