Nigel Reade

Nigel has been in the Pharmaceutical industry since 2006, covering all aspects of QA, GMP and GDP. He has worked for a variety of Pharmaceutical companies, in roles that cover GDP requirements, project management of complex projects, the full range of operational aspects of GDP, products requiring a Controlled Drug (CD) Licence, auditing and training.
In his role at HTF, Nigel works as an RP, RPi and QA Manager as well as managing larger GDP projects with clients. He specialises in the design and operation of Quality Management Systems, ensuring that these are tailored to a client’s products and internal processes whilst ensuring compliance with the latest guidelines and regulations. Nigel is active in both the UK (MHRA) and Ireland (HPRA) and familiar with the regulations in both territories.