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WSQMS
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Projects
Clinical Research *
Clinical Reporting
Product Development
Real World Data Research
Study Operations & Management
Trial Design & Planning
Commercialization *
Brand Planning & Activation
Customer Engagement
Finance & Investment *
Financial Services
Investment Banking
Market Access & Policy *
Global Market Access
Government Policy
Medical Affairs *
Defining the Value of Medical Affairs
Evidence Generation
Scientific Communications Development
Strategic Communications Planning
Strategic Stakeholder Engagement
Pharmacovigilance *
Risk Management
Safety Systems
Quality & Mfg *
Facilities & Equipment
Production & Supply Chain
Quality Management
Testing & Release
Regulatory *
Compliance
Labeling & Promotions
Maintenance & Renewals
Transparency & Disclosure
Technology & Operations *
Automation & Efficiency
Data & Analytics
Digital Health Solutions
Early Development
Informatics Infrastructure
Operations
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WSQMS
Pioneering Excellence in Global Drug Information and Quality Management Solutions
Specializing in the intricate field of drug information, this company is a global leader in quality management and strategic drug development solutions. Founded in 2012, their team consists of experts who collectively bring over two decades of experience in the pharmaceutical and biotech industries. Their robust knowledge extends throughout the entire lifecycle of drug development projects, from manufacturing and pre-clinical studies to post-approval commitment trials.
With a proven track record of advisory roles with key regulatory bodies such as the FDA, EMA, NMPA, BfArM, and Swissmedic, as well as organizations including WHO, OECD, CTTI, and ACRES, the company ensures their clients stay abreast of the latest methodologies and comply with evolving regulations. Their services encompass critical areas like GMP/GDP, GLP, GPV audits across numerous global regions including the US, Europe, China, India, Japan, Southeast Asia, Australia, and South America, positioning them uniquely in the market.
Pioneering Excellence in Global Drug Information and Quality Management Solutions
Specializing in the intricate field of drug information, this company is a global leader in quality management and strategic drug development solutions. Founded in 2012, their team consists of experts who collectively bring over two decades of experience in the pharmaceutical and biotech industries. Their robust knowledge extends throughout the entire lifecycle of drug development projects, from manufacturing and pre-clinical studies to post-approval commitment trials.
With a proven track record of advisory roles with key regulatory bodies such as the FDA, EMA, NMPA, BfArM, and Swissmedic, as well as organizations including WHO, OECD, CTTI, and ACRES, the company ensures their clients stay abreast of the latest methodologies and comply with evolving regulations. Their services encompass critical areas like GMP/GDP, GLP, GPV audits across numerous global regions including the US, Europe, China, India, Japan, Southeast Asia, Australia, and South America, positioning them uniquely in the market.
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