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  • Home
  • About Us
  • Services
    • Gxp Audit
      • GMP Audit
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      • GLP Audit
    • Quality Compliance Services
      • QMS
      • Audit and Inspection Readiness
      • Qualification and Validation
    • Regulatory Affairs
      • Submissions & Publishing
      • Artwork & Labelling
      • Regulatory Intelligence
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      • End-to-End Support
    • Pharmaceutical Engineering Services
      • Brownfield Facility Assessment
      • Greenfield Project Support
      • FAT Audit Support
  • Industries
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        • API
        • Excipient
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        • OSD (Tablet/Capsule)
        • Biological
        • Liquid formulation
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About Us

Home » About Us
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ABOUT US

We Provide Expert EU-GMP Services For You.

AIM INTELLIX GLOBAL SERVICE Pvt. Ltd. provides comprehensive end-to-end consultancy services for pharmaceutical facilities, supporting companies in achieving and maintaining compliance with international regulatory standards such as EU-GMP, USFDA, PIC/S, TGA, and UK MHRA.

Our Vision

To be a trusted global pharmaceutical consultancy, empowering clients to meet evolving regulatory requirements and achieve successful EU-GMP audits.

Our Mission

To deliver end-to-end pharmaceutical consultancy services—including plant design, QMS development, and regulatory audits—ensuring global compliance and operational efficiency.

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The company offers expert services in Quality Management Systems (QMS), qualification and validation, media fill studies, facility/process/system risk assessment, and professional training programs. AIM INTELLIX also supports clients with CAPA preparation, audit readiness, audit response, audit trigger management, and post-audit implementation support.

In addition, the company provides Gap Audits, Vendor Audit Support, Dossier Submission Assistance, and Plant Design/Layout Review to ensure facilities are designed and operated in full compliance with regulatory expectations.

Their expertise covers a wide range of pharmaceutical manufacturing platforms, including Vial Lines, Ampoule Lines, Eye Drop Lines, Lyophilized Products, Prefilled Syringes (PFS), Blow-Fill-Seal (BFS), Oral Solid Dosage (OSD), and other allied dosage forms.

By offering complete regulatory, quality, validation, and compliance solutions under one roof, AIM INTELLIX enables clients to access all required pharmaceutical consultancy services in a single basket—simplifying operations and ensuring efficient regulatory compliance.

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EU-GMP COMPLIANCE
BILINGUAL SUPPORT
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MAJOR PROJECTS
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WHY CHOOSE AIM INTELLIX

Your Pathway to EU-GMP Success

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End-to-End Solutions

We provide comprehensive support from initial plant design and facility upgrades to complete equipment qualification and validation.

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Experienced EU-GMP Experts

Our specialized team ensures your Quality Management Systems (QMS) and SOPs meet the highest global regulatory standards.

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Audit Readiness & Training

We offer bilingual documentation, custom training modules, and active support during official EU-GMP inspections to ensure certification success.

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Get In Touch:

support@aimintellixglobal.com

or

Call Us Via:

+91 94152 76508

INSTRUCTORS

Course Instructors

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Jane Seymour
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TESTIMONIALS

What Our Students
Have To Say

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David Owens
Designer

“Lorem ipsum dolor amet consectur elit adicing elit sed do umod tempor ux incididunt enim ad minim veniam quis sit nosrud citation laboris nisiste aliquip comodo perspiatix une omnis iste natus error sit voluptatem accusantium dolore que laudantum”.

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Bob Limones
Student

“Lorem ipsum dolor amet consectur elit adicing elit sed do umod tempor ux incididunt enim ad minim veniam quis sit nosrud citation laboris nisiste aliquip comodo perspiatix une omnis iste natus error sit voluptatem accusantium dolore que laudantum”.

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Tom Hurley
Content Creator
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Take a Video Tour to Learn
Intro of Campus

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AIM INTELLIX GLOBAL SERVICE Pvt. Ltd. provides end-to-end consultancy and implementation support for EU-GMP compliance across pharmaceutical facilities, including Injectables, OSD, and allied dosage forms.

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