Lotus Consulting Group

Lotus Consulting Group

Pharmaceuticals, Po Box 192, Riverview, Florida, 33568, United States, 1-10 Employees

lotusvalidation.com

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Who is LOTUS CONSULTING GROUP

Lotus Consulting Group has been in operation since March 2004 and provides comprehensive consulting and project management services in the fields of validation and quality assurance. Lotu...

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  • Po Box 192, Riverview, Florida, 33568, United States Headquarters: Po Box 192, Riverview, Florida, 33568, United States
  • 2004 Date Founded: 2004
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: Under $1 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Pharmaceuticals

SIC SIC Code: 8748

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Lotus Consulting Group Org Chart and Mapping

Employees

Billy Miller

President/Principal Consultant

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Frequently Asked Questions Regarding Lotus Consulting Group

Answer: Lotus Consulting Group's headquarters are located at Po Box 192, Riverview, Florida, 33568, United States

Answer: Lotus Consulting Group's official website is https://lotusvalidation.com

Answer: Lotus Consulting Group's revenue is Under $1 Million

Answer: Lotus Consulting Group's SIC: 8748

Answer: Lotus Consulting Group has 1-10 employees

Answer: Lotus Consulting Group is in Pharmaceuticals

Answer: Lotus Consulting Group contact info: Phone number: Website: https://lotusvalidation.com

Answer: Lotus Consulting Group has been in operation since March 2004 and provides comprehensive consulting and project management services in the fields of validation and quality assurance. Lotus Consulting Group serves both well established and start-up companies in the pharmaceutical, biotech, medical device and cosmetic industries. Our strong team leadership and experience base can support and accommodate the specific needs of our customers. Lotus Consulting Group offers experienced validation, compliance, and quality assurance services. We can assume full accountability and responsibility for your project or assist you with select project components of your choice. In working with you, we draw on a wealth of qualifications to implement your program from inception to completion. We use project documentation consistent with the applicable regulatory requirements. From our broad range of capabilities, we will align the right resources to the required program elements to guarantee the most favorable results and to suit your needs. SERVICES: Validation Master Plans Compliance Assessments Validation Protocols / Reports 21 CFR Part 11 Compliance Validation Field Execution EU / EC Compliance Equipment Qualification GAMP 4 Compliance Utility System Validation Quality System Action Plans Facility Qualification PAI Readiness Review Computer System Validation FDA / 483 / Warning Letter Responses Cleaning Validation Consent Decree / AIP Follow-up Process Validation Technology / Method Transfer Gap Analysis Calibration / PM Programs Standard Operating Procedures Data Tracking / Trending

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