In Consulting Services

PharmaNet offers a comprehensive range of early- and late-phase consulting services on topics including: international regulatory affairs; scientific and medical affairs; quality; risk management; chemistry, manufacturing and controls; as well as biopharmaceutical investor issues.

Biography

Thomas J. Noto

Executive Director, Document Management and Publishing
504 Carnegie Center
Princeton, NJ 08540
USA

Tel: 202 835 1352
Fax: 609 720 7900
E-mail: tnoto@pharmanet.com

Expertise: Regulatory submissions, New Drug Applications (NDAs), Investigational New Drug applications (INDs), electronic document management technology

 

Mr. Noto has more than 14 years of experience with electronic information management systems, including more than a decade in the pharmaceutical industry. At PharmaNet, Mr. Noto directs the regulatory submissions group, and advises clients on the generation of NDAs and INDs. In an earlier role, he implemented electronic document management systems that have enabled PharmaNet to comply consistently with both FDA and client requirements.

 

Mr. Noto is a member of the Drug Information Association (DIA). He is a frequent contributor of papers on electronic submissions to conferences held by DIA and other noted industry organizations.

 

PharmaNet Development Group, Inc.504 Carnegie Center, Princeton, NJ 08540Tel 609 951 6800Fax 609 514 0390