Piety Rocha Email & Phone Number | With over 20 years of experience in the pharmaceutical industry, I am a seasoned regulatory affairs professional with a proven track record of delivering successful outcomes for complex and challenging projects. I have extensive knowledge and expertise covering innovative and generic prescription medicines across multiple therapeutic areas. Currently, I am the Director Head of Regulatory Affairs and Country VDC Head at PharmaLex, a leading global provider of regulatory affairs and development consulting services offering regulatory solutions for the pharmaceutical and biotechnology sectors. In this role, I lead and manage a team of regulatory affairs specialists, oversee high-quality submissions for ANZ, and provide strategic guidance and support to clients across multiple therapeutic areas and regions. I also manage and execute regulatory projects for a diverse portfolio of clients, including generics manufacturers, innovators, and biosimilars developers. I am passionate about delivering regulatory excellence and ensuring patient access to safe and effective medicines.

Piety Rocha

With over 20 years of experience in the pharmaceutical industry, I am a seasoned regulatory affairs...
Sydney, Sydney, Australia

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Piety Rocha’s Location Sydney, Sydney, Australia

Piety Rocha’s Current Industry Cencora Pharmalex

Piety Rocha’s Prior Industry Pharmalex | Sanofi | Alphapharm | Abbott Laboratories

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Director Head of Regulatory Affairs

2021-04-01 00:00:00 - Present

Regulatory Affairs Manager

2021-03-01 00:00:00 - 2022-12-01 00:00:00

Regulatory Affairs Manager

2015-07-01 00:00:00 - 2022-03-01 00:00:00

Head Regulatory Affairs Australia

2010-08-01 00:00:00 - 2015-01-01 00:00:00

Senior Quality Assurance

1996-01-01 00:00:00 - 2001-12-01 00:00:00

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Piety Rocha is a With over 20 years of experience in the pharmaceutical industry, I am a seasoned regulatory affairs professional with a proven track record of delivering successful outcomes for complex and challenging projects. I have extensive knowledge and expertise covering innovative and generic prescription medicines across multiple therapeutic areas. Currently, I am the Director Head of Regulatory Affairs and Country VDC Head at PharmaLex, a leading global provider of regulatory affairs and development consulting services offering regulatory solutions for the pharmaceutical and biotechnology sectors. In this role, I lead and manage a team of regulatory affairs specialists, oversee high-quality submissions for ANZ, and provide strategic guidance and support to clients across multiple therapeutic areas and regions. I also manage and execute regulatory projects for a diverse portfolio of clients, including generics manufacturers, innovators, and biosimilars developers. I am passionate about delivering regulatory excellence and ensuring patient access to safe and effective medicines.