One Stop Pharma Solution | Turnkey project | Global Leader in Regulatory Audit – Compliance, Regulatory Affairs services | GxP services | New Product Development | Bridging Academia and Pharma Industry for Innovation | Internship Project Support | Pharma Industry visit Assistance | Placement Assistance | Career Development Programs | Workshops | Webinars | Digital marketing | Social Media marketing | AI
CEO & Founder
DR. YAUVAN PANCHOLI (M.Sc., Ph. D.)
A Doctorate in Chemistry, highly versatile and a seasoned professional with over 20 years of extensive experience of well known Pharmaceutical industries.
Professional Experience
Educational Qualification
- Doctorate in "Supramolecular Chemistry"
- Publication in National and International Journals
- University Recognized Ph.D. Guide
Achievements
Greenfield projects, recurrent history of successful completion of USFDA with "Zero 483", EUGMP, MHRA, TGA, PICs, WHO and other regulatory agency audits.
Overview
Pharmex is the One Stop Solution for Pharma Industries, Healthcare industries, Graphic designing, Digital marketing, Artificial intelligence to provide various services under one roof.
Our group is backed up with high skilled professionals to provide scientific & quality solutions for pharmaceutical industries to achieve compliance for Local & International standards i.e. USFDA, EUGMP, MHRA, TGA, PICS, WHO and other regulatory standards. Our paramount goal is to provide quality work, which is well accepted globally.
Mission
To support Pharmaceutical companies GLOBALLY and be sustainable by providing various services that meet the highest level of quality standards in an efficient manner.
- Honest and ethical services/audits
- Fully committed to the client's requirements
Vision
Providing prompt, efficient and innovative pharma services solutions for the clients through integrity, honesty & uncompromising commitment to quality.
- Global workforce with local presence hence most cost effective
Our Services
Pharmex is the One Stop Solution for Pharma Industries, Healthcare industries, Graphic designing, Digital marketing & Artificial intelligence, etc.
New plant setup as per current regulatory requirement, renovation or expansion of existing plant, R&D setup and DSIR approval process, contract testing lab setup, CRO setup.
Formulation development support and troubleshooting, guidance on biostudy design, selection of CRO for BA/BE study, scaleup studies and technology transfer activities.
Audit, gap assessment & compliance assistance for all regulatory agency, third-party audit, vendor audit, internal audit, effective QMS implementation.
Preparation, compilation and submission of dossier, DMF as per latest country specific guideline, regulatory query response support, review of dossier, DMF, ANDA documents.
Technical support for any requirements of ADL and QC, guidance on analytical method development (AQBD), analytical method validation/verification, method transfer activities.
Industrial training/tour, online consultation from senior industrial & academic expert, technical training (onsite and offsite), recruitment of skilled manpower.
Our Expertise
