Pharmazone is a leading Consulting company with a strong legacy of trust amongst the global Pharmaceutical & Life Sciences industry. The company specializes in Regulatory Affairs, Pharmacovigilance, GxP Compliance solutions to clients for improving patient’s lives through unique Commit-Collaborate-Carry Model.
 
As a Regulatory Specialist, we assist our clients with solutions like Regulatory Intelligence & Strategy, Medical Writing, Submission & Publishing, Artwork, Labelling, translation, Health Authority interactions, and all post-approval requirements including an end to end Pharmacovigilance services like case management, Aggregate Reports, Signal Detection, MICC, etc. Our objective is to help large, medium & small-size life science companies in efficient execution & compliance of their drug development plans and Post-Approval Requirements for regulated markets and the developing world. 

Global Regulatory Landscape is dynamic and our compliance services (GXP) play a vital role for clients. Being a trendsetter in GCP Auditing & Consulting, Pharmazone has successfully carried out 2000+ projects for Clinical Monitoring (Bioequivalence, Late Phase), Study Design, Audits, CRO setup & Up-gradation & Programme Management. Our GMP Solutions include Audits, Report Library, Quality Consulting, USFDA/EMA/PICS/WHO accreditation Support, CSV & Engineering Services including Plant Setup & Upgradation. 

Though Client's trust is our biggest recognition, our hard work-filled journey has brought us various awards like "Best HealthCare Brand" by CMO Asia -ABP News, “Top 10 Clinical Research Provider” by Silicon India.

"Value Creation by Right Solutions” is Working Mantra at Pharmazone. The expert team at our global locations (INDIA, USA, EUROPE, CANADA and CHINA) have served 450+ Clients to satisfaction and we look forward to serving you!

Life Sciences

Pharmaceutical

Pharmazone

Pharmazone's headquarters in Ahmedabad, India

This department focuses on identifying growth opportunities and fostering relationships to expand the organization's market presence.

Business Development

The Clinical Research Team at Pharmazone is responsible for overseeing and managing clinical trials to ensure they are conducted in compliance with Good Clinical Practice (GCP) guidelines. This involves activities such as study design, clinical monitoring, auditing, and project management for bioequivalence and late-phase studies. The team collaborates with contract research organizations (CROs), manages clinical research associates, facilitates GCP audits, and supports the setup and upgrading of clinical research operations. Their work ensures the successful execution and regulatory compliance of clinical trials, contributing to the efficient development of pharmaceutical products.

Clinical Research Team

This department oversees global manufacturing practices and ensures compliance through auditing and project management.

GMP Services

This department is responsible for monitoring the safety and efficacy of pharmaceutical products to ensure patient safety.

Pharmacovigilance

This department conducts and manages clinical trials to evaluate the safety and efficacy of new medical treatments.

Clinical Research

The Business Development Team at Pharmazone is responsible for identifying and cultivating new business opportunities, maintaining client relationships, and expanding the company’s market presence globally. They work collaboratively to develop strategic partnerships, drive sales initiatives, and explore new markets, ensuring Pharmazone's growth and alignment with industry trends. This team plays a crucial role in introducing Pharmazone’s regulatory, compliance, and consulting services to potential clients across various regions.

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Other teams

Clinical Research Team

GMP Services

Pharmacovigilance

Clinical Research

Business Development Team