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DUCK FLATS

Duck Flats

Pharmaceuticals, 245 East Main Street, Elbridge, New York, 13060, United States, 11-50 Employees

dfpharma.com

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phone no Phone Number: 90********

Who is DUCK FLATS

DUCK FLATS Pharma is an R&D consulting and contract firm. Our specific expertise is in strategic drug development with a special focus on non-clinical development to clinical pharmacology...

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  • 245 East Main Street, Elbridge, New York, 13060, United States Headquarters: 245 East Main Street, Elbridge, New York, 13060, United States
  • 2001 Date Founded: 2001
  • 11-50 Employees: 11-50
  • dollar-icon Revenue: $10 Million to $25 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Pharmaceuticals

SIC SIC Code: 2678 | NAICS Code: 451130 | Show More

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DUCK FLATS Org Chart and Mapping

Employees
Karen Ralston

Karen Ralston

Sr. Manager of Finance & Administration

J Goyette

J Goyette

Tech Writer/Document Review Associate

Barry Koplowitz

Barry Koplowitz

Senior Scientist, Pharmacokinetics

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Frequently Asked Questions Regarding DUCK FLATS

Answer: DUCK FLATS's headquarters are located at 245 East Main Street, Elbridge, New York, 13060, United States

Answer: DUCK FLATS's phone number is 90********

Answer: DUCK FLATS's official website is https://dfpharma.com

Answer: DUCK FLATS's revenue is $10 Million to $25 Million

Answer: DUCK FLATS's SIC: 2678

Answer: DUCK FLATS's NAICS: 451130

Answer: DUCK FLATS has 11-50 employees

Answer: DUCK FLATS is in Pharmaceuticals

Answer: DUCK FLATS contact info: Phone number: 90******** Website: https://dfpharma.com

Answer: DUCK FLATS Pharma is an R&D consulting and contract firm. Our specific expertise is in strategic drug development with a special focus on non-clinical development to clinical pharmacology. We cover all therapeutic areas. Our group of experts can help set up and implement a strategic development plan focusing on the mechanism of action, efficacy and pharmacokinetics of the drug or biotechnology compound being developed. We use this focus to support the clinical indication and to build a regulatory package that will support successful IND and NDA/CTD approvals.

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