About
Pharmazone
Leading the way in pharmaceutical innovation, Pharmazone is dedicated to advancing health and wellness through cutting-edge research and superior quality products. Our commitment to excellence and patient-centric approach drives us to deliver impactful solutions that improve lives worldwide.
We strive to improve lives globally through
cutting-edge technologies and a passionate team of experts. Discover the future of healthcare with Pharmazone.
The Journey of
Pharmazone
2024
- Known as the most trusted integrated GxP & Regulatory Consulting firm Globally
2018
- Initiated Concept Development Support – New Service
- Expanded training portfolio to include e-Learning, workshops and complete Training support
- Recognized by one of the most reputed healthcare magazines- Silicon India under "10 Most Promising Clinical Trials Solution Providers – 2018”
- Awarded with “Brand Leadership Award” in healthcare category by CMO ASIA 2018
2017
- Moved to our new office location
- 1000 monitoring projects milestone
- Software support to Pharma Manufacturing
- Opened office in Canada
2016
- Introduced PV support
- Represented as Speaker on “Clinical Research” at CPhI Wordwide-2016, Barcelona
- CRO Development Greenfield projects
- Retrofitting for CROs
- Software support to CRO
2015
- Initiated GMP training
- 500 monitoring projects milestone
- Started QMS Review audit of CRO
- Introduced GMP Monitoring
- Conducted projects in Canada, USA, China, Jordan, Spain, Sweden, Romania
2014
- Dossier Licensing
- Contract manufacturing support
- Started Regulatory Services and Training
- Initiated GMP audits
2013
- Auditing Phase-I CROs
- Provided GCP/GLP Trainings
- Initiated API and RLD Sourcing
- CRO Set up & Upgradation
2012
- Emerged as a very strong player into Clinical Trials and specialized BE studies
- Performed many Retrospective GCP, Feasibility-CRO selection, GAP, Pre-Inspection Audits
- Became preferred partner for Middle East and EU Clients
- Created massive data base for conducting specialized Clinical Trials
- Site Management for clinical trials
2009
- Conceptualized the idea of providing independent Auditing and clinical monitoring
- Commenced operation in Monitoring of Clinical Phases
- Conceptualized the idea of providing Bio-analytical monitoring
- Became very strong player in Auditing and Monitoring of BA/BE Studies and Clinical Trials
- Tie up with Regulatory experts in India, EU, USFDA