SriSai Biopharmaceutical Solutions

Sri Sai Biopharmaceutical Solutions

Biotechnology, 320 Montevue Ln, Frederick, Maryland, 21702, United States, 11-50 Employees

srisaibiopharma.com

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Who is SRISAI BIOPHARMACEUTICAL SOLUTIONS

SriSai Biopharmaceutical Solutions (SBS) has been providing comprehensive support services to the life sciences industry for over 15 years in the areas of supply chain management. These s...

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  • 320 Montevue Ln, Frederick, Maryland, 21702, United States Headquarters: 320 Montevue Ln, Frederick, Maryland, 21702, United States
  • 2002 Date Founded: 2002
  • 11-50 Employees: 11-50
  • dollar-icon Revenue: $10 Million to $25 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Biotechnology

SIC SIC Code: 7389

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Frequently Asked Questions Regarding SriSai Biopharmaceutical Solutions

Answer: SriSai Biopharmaceutical Solutions's headquarters are located at 320 Montevue Ln, Frederick, Maryland, 21702, United States

Answer: SriSai Biopharmaceutical Solutions's official website is https://srisaibiopharma.com

Answer: SriSai Biopharmaceutical Solutions's revenue is $10 Million to $25 Million

Answer: SriSai Biopharmaceutical Solutions's SIC: 7389

Answer: SriSai Biopharmaceutical Solutions has 11-50 employees

Answer: SriSai Biopharmaceutical Solutions is in Biotechnology

Answer: SriSai Biopharmaceutical Solutions contact info: Phone number: Website: https://srisaibiopharma.com

Answer: SriSai Biopharmaceutical Solutions (SBS) has been providing comprehensive support services to the life sciences industry for over 15 years in the areas of supply chain management. These services include storage and global distribution, secondary packaging and labeling, validation and consultation. SBS currently serves clients from both the government and commercial sectors with adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), Good Documentation Practices (GDP), Food and Drugs Administration (FDA) administration regulations and in accordance with client requirements. These activities are in support of Phase I, and/or II, and/or III clinical studies (Investigational New Drug also known as IND or New Drug Application also known as NDA).

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