+1 516.933.0900

In the complex pharmaceutical industry, a combination of expertise, care and attention to detail are mandatory for any company that wants to successfully maneuver through the bureaucratic and regulatory maze.

That’s where GYMA’s Scientific & Regulatory Affairs team comes in. From the beginning of R&D, through analytical development, to pre- and post-approval regulatory submissions, our team members can guide your project to a successful outcome.

GYMA clients receive all of the latest technical information needed. If you are a manufacturer, you can have confidence that our team is fully versed in the latest FDA and US DEA regulations and guidelines. It’s why we can provide you with keen insight about:

  • Drug Master File reviews
  • API imports
  • Facility inspections
  • Establishment registrations
  • Drug listings

Gyma Laboratories of America, Inc.

Corporate Headquarters

135 Cantiague Rock Road
Westbury, NY 11590
Telephone: +1 516-933-0900
Facsimile: +1 516-933-1075
Email: Sales@GYMA.com
URL:

China Office

C7-10 Qilu Int’l Bldg,
180 Quancheng Rd, Ji’nan City
Shandong Province, China, 250011
Contact: Luke Tou
Telephone: +86-18018661683
Email: luke.tou@gyma.com

India Office

Anna Nagar, Chennai – 600040,
Tamilnadu, India
Patented products available for R&D use as permitted under 35 USC 271 (e) (1)
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