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Company Intro

Your Trusted Regulatory Partner

We are a team of experts in providing global regulatory services for Pharmaceuticals, Medical Device, and Cosmetics on time, ensuring regulatory compliance. Connect with us today for more information.

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Global Regulatory Solutions

Empowering Regulatory Excellence Since 2017

We specialize in providing comprehensive regulatory affairs solutions for Pharmaceuticals, Nutraceuticals, Medical Devices, and more. Our expert team combines industry knowledge with a commitment to help clients through the complexities of global regulatory compliance, ensuring successful approvals and market entry. With a focus on quality and client satisfaction, we help businesses to thrive in a competitive world.

At Medwisdom LifeSciences Pvt Ltd, we are dedicated in consulting for the Pharmaceutical, Medical Device, Cosmetics, and Food Industries. With a team of industrial experts, boasting over 20 years of experience, we offer support across diverse domains, including development, technology transfer, regulatory affairs, intellectual property, clinical and non-clinical studies, manufacturing, and facility audits.

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Our Core Ethics

These values guide every decision, interaction, and deliverable we provide.

Quality

Every deliverable meets the highest global standards — no compromises.

Reliability

Consistent delivery, clear updates, and dependable timelines — always.

Transparency

Full visibility into processes, progress, and challenges at every step.

Excellence

Continuously raising the bar through precision and innovation.

Team Work

True collaboration — internal & with clients — for shared success.

Punctuality

Deadlines respected — high-quality work delivered exactly on time.

Our Specialized Services

Regulatory Submissions & Dossier

Excellence in Regulatory Submissions and Dossier Preparation

Our strength lies in delivering exceptional regulatory submissions and dossier preparation services including:

  • Expertise in handling CTD, eCTD, ACTD, and country-specific submission requirements.
  • Compilation and review of dossiers.
  • Efficiently addressing technical queries from global regulatory authorities to ensure timely approvals.

Global Quality Assessment and Monitoring Services

Medwisdom serves as a trusted partner for international pharmaceutical companies sourcing products from India. Our expert auditors, with over 20 years of experience, conduct thorough quality assessments and audits of Indian pharmaceutical manufacturers.

We identify gaps, recommend corrective measures, and ensure compliance with global standards, fostering trust and quality assurance.

Global Quality Assessment
Technical & Regulatory Services

Our Expertise in Technical and Regulatory Services

Medwisdom offers a wide range of technical and regulatory services to streamline operations for the life sciences sector. Our key services include:

  • Expertise in preparing Drug Master Files (DMF)
  • Conducting internal audits, pre-audits, and preparation for regulatory inspections
  • Providing professional training in GMP compliance, technical skills, and personality development

Driving Innovation and Compliance

At Medwisdom, we aim to create a bridge between pharmaceutical innovation and regulatory compliance. By focusing on quality, technical expertise, regulatory adherence, and skill development, we contribute to the sustainable growth of our clients.

Connect with us today for fast submissions and timely approvals.

Innovation & Compliance
Milestones

Our Achievements

100+

Projects Successfully Completed

15+

Countries Served

20+

Years of Combined Expertise

100%

Compliance Success Rate