Certara Synchrogenix

Certara Synchrogenix

Pharmaceuticals, 100 Overlook CTR, Wilmington, Delaware, 08540, United States, 201-500 Employees

synchrogenix.com

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phone no Phone Number: 30********

Who is CERTARA SYNCHROGENIX

Certara Synchrogenix assures and accelerates the approval of and access to medical innovations through a unique combination of customized regulatory strategy, document authoring, medical ...

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  • 100 Overlook CTR, Wilmington, Delaware, 08540, United States Headquarters: 100 Overlook CTR, Wilmington, Delaware, 08540, United States
  • 1986 Date Founded: 1986
  • 201-500 Employees: 201-500
  • dollar-icon Revenue: $250 Million to $500 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Pharmaceuticals

SIC SIC Code: 7389 | NAICS Code: 561410 | Show More

checked-icon Does something look wrong? Fix it. | View contact records from CERTARA SYNCHROGENIX

Certara Synchrogenix Org Chart and Mapping

Employees

Kara Sorrell

Senior Regulatory Writer

Nellie Forwood

Principal Regulatory Writer, Cmc

Peyton Petrillo

Talent Acquisition Coordinator

Jennifer McElhattan

Principal Regulatory Writer

Mark Bowlby

Director, Global Submissions

Carlos Rousselin

Assoc Principal Regulatory Writer

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Frequently Asked Questions Regarding Certara Synchrogenix

Answer: Certara Synchrogenix's headquarters are located at 100 Overlook CTR, Wilmington, Delaware, 08540, United States

Answer: Certara Synchrogenix's phone number is 30********

Answer: Certara Synchrogenix's official website is https://synchrogenix.com

Answer: Certara Synchrogenix's revenue is $250 Million to $500 Million

Answer: Certara Synchrogenix's SIC: 7389

Answer: Certara Synchrogenix's NAICS: 561410

Answer: Certara Synchrogenix has 201-500 employees

Answer: Certara Synchrogenix is in Pharmaceuticals

Answer: Certara Synchrogenix contact info: Phone number: 30******** Website: https://synchrogenix.com

Answer: Certara Synchrogenix assures and accelerates the approval of and access to medical innovations through a unique combination of customized regulatory strategy, document authoring, medical communications and publications, and operations solutions. Our proven record of success is built on an unrivaled commitment to quality and compliance combined with the use of advanced technologies to enhance speed and efficiency. With industry experts across the full product development lifecycle in North America, Europe and Asia Pacific, we provide the flexibility, scalability and round-the-clock support sponsors need to meet changing requirements and timelines.

Answer:

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