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"PharmAdvis Solutions LLP provides comprehensive Regulatory Solutions for global compliance, Quality Management for GMP excellence, and Training & Development to enhance team expertise in regulatory and quality systems."

WELCOME!
PharmAdvis is a firm specializing in advising, consulting, and training within the pharmaceutical industry.

INTRODUCTION

MISSION

  • Ensuring successful regulatory submissions and approvals for global markets through meticulous planning and execution.
  • Promoting industry best practices and upholding the highest standards of quality and compliance to meet international regulatory requirements.
  • Supporting pharmaceutical companies in navigating the complexities of regulatory landscapes, enabling them to bring safe and effective products to market swiftly.
  • Offering tailored training programs that build capabilities in regulatory filing strategies, quality management systems, and GMP remediation.
  • Collaborating closely with clients to develop customized strategies that enhance operational efficiency, mitigate risks, and drive sustainable growth in an ever-evolving industry.
  • By maintaining a client-centric approach and leveraging decades of industry experience, we aim to be a trusted partner in driving excellence and innovation across the global pharmaceutical sector.
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VISION

What We Do

Consulting Service

Regulatory Solution

At PharmAdvis Solutions LLP, we provide end-to-end regulatory services that ensure your product’s compliance with global regulatory standards. Our team assists with the development of regulatory strategies tailored to specific regions, guiding clients through the entire regulatory submission process, from initial filings to post-approval compliance.

Quality Management

We provide a comprehensive range of quality management services designed to help companies implement and maintain robust quality systems. Our services focus on ensuring compliance with Good Manufacturing Practices (GMP), preparing for regulatory inspections, and developing risk management frameworks that mitigate quality-related issues.

Training and Development

Our specialized training programs are designed to keep your regulatory and quality teams up-to-date with the latest industry standards and practices. We offer hands-on training in regulatory filing strategies, quality management systems, and international regulatory requirements (e.g., ICH guidelines).

Reviews From Our Happy Clients
*”Working with PharmAdvis Solutions LLP has been a game-changer for our business. Their team of experts guided us through the complex regulatory submission process with precision and professionalism. Thanks to their in-depth knowledge and strategic approach, we successfully secured approvals for our product in multiple international markets.

The quality management solutions they implemented have transformed our operations, ensuring we meet all global compliance standards effortlessly. Their training programs were incredibly comprehensive, keeping our team up-to-date with the latest industry best practices.

PharmAdvis is more than just a consulting firm – they are a true partner dedicated to our success. We highly recommend their services to any pharmaceutical company looking for a trusted, reliable, and expert-driven partner!”*

Carol Oliveira

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