ISPE European Regulatory Affairs Advisor will be Bryan Wright.

Press Release Summary:



Effective April 1 of 2011, Bryan Wright will join ISPE as European Regulatory Affairs Advisor. He will act as liaison between ISPE and European regulatory authorities, helping expand relationships between regulatory bodies and ISPE, shaping ISPE educational offerings, and keeping ISPE Members informed of relevant regulatory developments originating from European regulatory authorities. ISPE President and CEO Bob Best called Bryan's years of regulatory experience, "invaluable."



Original Press Release:



Bryan Wright Named New ISPE European Regulatory Affairs Advisor



--Long-Time MHRA Official to Offer Insight, Guidance--

(TAMPA, FLORIDA, USA) - ISPE, a global not-for-profit association of 22,000 pharmaceutical science and manufacturing professionals, today announced that Bryan Wright will join ISPE as European Regulatory Affairs Advisor, effective 1 April 2011. In his new capacity, Mr. Wright will act as liaison between ISPE and European regulatory authorities to help expand relationships between regulatory bodies and ISPE, shape ISPE educational offerings, and keep ISPE Members informed of relevant regulatory developments originating from European regulatory authorities.

"We are extremely fortunate to add Bryan Wright to ISPE's strong regulatory team," said Bob Best, ISPE President and CEO. "Bryan's 22 years of regulatory experience will be invaluable to ISPE as we continue our mission to help our Members facilitate global GMP solutions that will bring the pharmaceutical industry into the future."

Mr. Wright comes to ISPE after taking early retirement from the MHRA. He joined the MHRA as an Inspector in 1989 and for the last five years has been Group Manager for the GMP & GDP Inspectorate. As a senior manager within the MHRA, Mr. Wright had oversight of the significant growth in Inspectors in that Agency in recent years in response to regulatory demand.

Mr. Wright has previous experience in community and hospital pharmacy and holds a degree in pharmacy and a Masters in pharmaceutical sciences. Over the course of his 22 years with the MHRA, Mr. Wright has managed most areas of the Inspectorate at various times, and his regulatory career encompasses GMP, GDP, GCP, GPvP, and the GLP monitoring authority.

About his early retirement from MHRA and subsequent role with ISPE, Mr. Wright said: "I am looking forward to new challenges, including utilizing the skills and knowledge I have gained from my years in the regulatory field in my new role with ISPE."

Mr. Wright assumes the duties of the European Regulatory Affairs Advisor position from John Berridge, who will now turn his full attention to his role as Project Manager for the Society's PQLI® Initiative, as well as other strategic projects for ISPE. Mr. Wright joins Bob Tribe, Asia-Pacific Regulatory Affairs Advisor, on ISPE's Regulatory Affairs team.

About ISPE
ISPE, the International Society for Pharmaceutical Engineering, is a Society of 22,000 pharmaceutical professionals in 90 countries who use expert knowledge to create high-quality, cost-effective GMP solutions. ISPE is "Connecting a World of Pharmaceutical Knowledge" by providing Members with opportunities to develop their technical knowledge, exchange practical experience within their community, enhance their professional skills, and collaborate with global regulatory agencies and industry leaders. Founded in 1980, ISPE offers online learning opportunities for a global audience and has its worldwide headquarters in Tampa, Florida, USA; its European office in Brussels, Belgium; an Asia Pacific office in Singapore; and its newest office in Shanghai, China. Visit www.ISPE.org for additional Society news and information.

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