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Omnicia, Inc.
Omnicia, Inc.
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Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
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Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
Technology & Operations *
Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
Operations
Informatics Infrastructure
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Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
Labeling & Promotions
Maintenance & Renewals
Compliance
Transparency & Disclosure
Commercialization *
Customer Engagement
Brand Planning & Activation
Market Access & Policy *
Government Policy
Global Market Access
Pharmacovigilance *
Safety Systems
Risk Management
Finance & Investment *
Financial Services
Investment Banking
Quality & Mfg *
Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
Technology & Operations *
Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
Operations
Informatics Infrastructure
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About
One Crossroads Drive, Suite 301B, Bedminster, NJ 07921, USA
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Omnicia, Inc.
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Streamline Your Regulatory Submissions with Omnicia's Intuitive Software Solutions
Omnicia provides innovative software solutions and expert consulting services to simplify the complex global electronic submission process for life sciences companies. Our intuitive software electronically creates, publishes, and views compliant documents, reports, and eCTD submissions for US, EU, and CA review.
Omnicia was founded by industry veterans in 2001 to reduce the high costs traditionally associated with regulatory submissions. With over 40 years of combined experience, our management team supports leading biotech, pharmaceutical, and medical device companies with electronic publishing, FDA negotiations, 21 CFR Part 11 compliance, and more.
Let Omnicia's expertise streamline your next regulatory submission with our elegant and easy-to-use software tools. Contact us today to simplify your electronic document management needs.
Streamline Your Regulatory Submissions with Omnicia's Intuitive Software Solutions
Omnicia provides innovative software solutions and expert consulting services to simplify the complex global electronic submission process for life sciences companies. Our intuitive software electronically creates, publishes, and views compliant documents, reports, and eCTD submissions for US, EU, and CA review.
Omnicia was founded by industry veterans in 2001 to reduce the high costs traditionally associated with regulatory submissions. With over 40 years of combined experience, our management team supports leading biotech, pharmaceutical, and medical device companies with electronic publishing, FDA negotiations, 21 CFR Part 11 compliance, and more.
Let Omnicia's expertise streamline your next regulatory submission with our elegant and easy-to-use software tools. Contact us today to simplify your electronic document management needs.
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One Crossroads Drive, Suite 301B, Bedminster, NJ 07921, USA
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