Pharmazone
Kuldeep Dudhrejiya is a skilled clinical research professional with extensive experience in various roles within the pharmaceutical sector. Currently serving as a Clinical Research Associate and Senior Project Coordinator at Pharmazone since April 2021, Kuldeep previously held the position of Sr. Research Assistant at Veeda Clinical Research from April 2019 to April 2021. Prior experience includes working as a Stability Study Officer at Otsuka Pharmaceutical India Pvt. Ltd. from May 2018 to February 2019, where Kuldeep focused on the analysis of parental products in the stability department. Educational qualifications include an Advanced Post Graduate Diploma in Clinical Research from Imperial Institute of Clinical Research in 2019, a Post Graduate Diploma in Sophisticated Instrumentation Techniques for Pharma from Saurashtra University in 2018, and a Bachelor's degree in Chemistry from Saurashtra University, completed in 2017.
Pharmazone
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!