FDA Regulations, Best Practices for Medical Device Design, Manufacturing, Quality and Supplier Control to Be Taught by Former Agency Inspectors July in Delaware

WILMINGTON, Del., May 9, 2011 — Medical device R&D labs and manufacturers now have a personal resource for answers to the often confusing maze of FDA regulations outlined in the Agency’s Quality System Regulations (21 CFR 820).
EduQuest – a global team of FDA compliance experts…

Probactive Biotech, Inc. Announces an Agreement to Co-Develop Novel Biopharmaceuticals for Cancer with Dalat Nuclear Research Institute of Vietnam

GARDEN GROVE, Calif., June 22, 2010 — Probactive Biotech, Inc., a Garden Grove, California-based corporation, has entered into an agreement with Dalat Nuclear Research Institute to co-develop a number of cancer drugs, utilizing combinations of antitumor antibodies and antitumor radioacti…

Voler Systems Reports 50% Growth

SUNNYVALE, Calif., Oct. 28, 2009 — Voler Systems (http://www.volersystems.com), a provider of electronic design consulting services, today reported 50% growth over the same period last year.
“Voler Systems’ consulting for medical devices continues to drive our strong result…

Voler Systems Continues Investments and Expands Services

SUNNYVALE, Calif., April 7, 2009 — Voler Systems (http://www.volersystems.com) has launched a “Quality System for Medical Device Innovation Program” which provides full-service consulting from concept and design to production of devices for human use. The current economic c…