Pharmavise Corporation Tech Stack

FDA compliance and quality consulting for pharma, biotech, and medical device firms

Business Consulting and Services Fort Lauderdale, Florida 11–50 employees Founded 2013 Privately Held

Pharmavise is a 20+ employee consulting firm focused on regulatory and quality operations across life sciences and healthcare. The tech stack reflects a compliance-heavy, project-driven operation: Veeva Vault and Veeva QMS for document and quality management, Medidata Rave for clinical data, statistical tools (JMP, Minitab, SAS, WinNonlin), and core collaboration via Microsoft and GitHub. The hiring mix skews heavily senior (19 of 27 tracked roles) across healthcare, engineering, legal, and research — indicating deep expertise delivery rather than volume scaling.

Tech Stack 23 technologies

Core StackFigma SAS Python GitHub Bitbucket Microsoft Project Microsoft Office Excel Medidata Rave Veeva Vault Minitab JMP Oscilloscope Multimeter SPICE SPC Lean Six Sigma WinNonlin Adobe Acrobat Teams Veeva QMS LinkedIn Zoho

What Pharmavise Corporation Is Building

◆Challenges

Ensuring compliance with fda regulations
Qms modernization
Complex compliance issues
Addressing gmp-related issues
Nda submission preparation
Optimizing manufacturing processes
Implementing new technologies
Risk mitigation for manufacturing processes
Complex product development lifecycle
Cross-functional project coordination

▲Active Projects

Contracting process improvement initiative
Design and validation of manufacturing equipment
Medical device product development and commercialization
Technical documentation and risk management
Continuous improvement of project governance
Signal detection activities
Risk management plan development
Implementation of new technologies
Medical device interface design
Digital tool design for connected systems

Hiring Activity

Minimal30 roles · 3 in 30d

Department

Healthcare

Engineering

Legal

Research

Quality

Sales

Design

Manufacturing

Seniority

Senior

Mid

Manager

Junior

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About Pharmavise Corporation

Pharmavise provides consulting services in regulatory affairs, quality systems management, and compliance remediation for pharmaceutical, biotech, and medical device companies, as well as government-sector clients. Founded in 2013 and based in Fort Lauderdale, Florida, the firm works across FDA compliance, computer system validation, data integrity, health authority inspection readiness, and vendor management. The active project portfolio spans medical device product development, manufacturing equipment validation, technical documentation, risk management planning, and QMS modernization. The firm operates with a senior-weighted team structure and hires across the US and Philippines.

HeadquartersFort Lauderdale, Florida

Company Size11–50 employees

Founded2013

Hiring MarketsUnited States, Philippines

Frequently Asked Questions

What tech does Pharmavise use for compliance and quality management?

Pharmavise uses Veeva Vault and Veeva QMS as core platforms for document and quality management, Medidata Rave for clinical data, and statistical analysis tools including JMP, Minitab, and SAS. Project coordination runs on Microsoft Project and Office.

What are Pharmavise's main service areas?

Core specialties include FDA compliance consulting, regulatory affairs, quality systems management, computer system validation, data integrity (ALCOA), health authority inspection readiness, vendor auditing, and medical device product development support.